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At Niagara, we’re looking for Team Members who want to be part of achieving our mission to provide our customers the highest quality most affordable bottled water.
Consider applying here, if you want to:
We offer competitive compensation and benefits packages for our Team Members.
Production OperatorThis position is responsible for daily operations of the production floor; ensuring the shift meets established safety, quality, and production goals in compliance with all applicable legal and food safety requirements.Essential Functions
Qualifications
*experience may include a combination of work experience and education
*experience may include a combination of work experience and education
Competencies
This position embodies the values of Niagara’s LIFE competency model, focusing on the following key drivers of success:
Education
Certification/License:
Foreign Language
Benefits
https://careers.niagarawater.com/us/en/benefits
Any employment agency, person or entity that submits a résumé into this career site or to a hiring manager does so with the understanding that the applicant's résumé will become the property of Niagara Bottling, LLC. Niagara Bottling, LLC will have the right to hire that applicant at its discretion without any fee owed to the submitting employment agency, person or entity.
Employment agencies that have fee agreements with Niagara Bottling, LLC and have been engaged on a search shall submit résumé to the designated Niagara Bottling, LLC recruiter or, upon authorization, submit résumé into this career site to be eligible for placement fees.
Official account of Jobstore.
At Niagara, we’re looking for Team Members who want to be part of achieving our mission to provide our customers the highest quality most affordable bottled water.
Consider applying here, if you want to:
We offer competitive compensation and benefits packages for our Team Members.
Production OperatorThis position is responsible for daily operations of the production floor; ensuring the shift meets established safety, quality, and production goals in compliance with all applicable legal and food safety requirements.Essential Functions
Qualifications
*experience may include a combination of work experience and education
*experience may include a combination of work experience and education
Competencies
This position embodies the values of Niagara’s LIFE competency model, focusing on the following key drivers of success:
Education
Certification/License:
Foreign Language
Benefits
https://careers.niagarawater.com/us/en/benefits
Any employment agency, person or entity that submits a résumé into this career site or to a hiring manager does so with the understanding that the applicant's résumé will become the property of Niagara Bottling, LLC. Niagara Bottling, LLC will have the right to hire that applicant at its discretion without any fee owed to the submitting employment agency, person or entity.
Employment agencies that have fee agreements with Niagara Bottling, LLC and have been engaged on a search shall submit résumé to the designated Niagara Bottling, LLC recruiter or, upon authorization, submit résumé into this career site to be eligible for placement fees.
Official account of Jobstore.
Founded in 1994, Silent-Aire is a technology-driven company that designs, engineers, and manufactures hyperscale cooling and modular data center solutions. Silent-Aire employs over 3000 people, with a total of 13 manufacturing facilities and over 1 million sq/ft of capacity in Edmonton, Alberta; Gilbert, Arizona; and Dublin, Ireland. There are sales/service centers in Seattle, Washington; Boardman, Oregon; Ashburn, Virginia; and Dublin, Ireland. Since May 2021, Silent-Aire has been a part of Johnson Controls' Data Center Solutions group. To learn more, please visit https://www.silent-aire.com/.
What you will do
You will be responsible for supervising and coordinating the activities of production and operation workers (approximately 50-75 employees), such as assemblers, inspectors, precision workers, machine operators, fabricators, and plant and system operators while ensuring that production schedules are created and completed on time, safely, and within budget.
How you will do it
Direct the manufacturing workforce to achieve production goals.
Enforce safety and sanitation regulations.
Anticipate production obstacles and manage team and stakeholders to overcome them.
Provide leadership and ownership of product quality while consulting with Quality staff and Engineers on quality issue while being accountable for the overall QA performance of the manufacturing unit.
Confer with management or subordinates to resolve worker problems, complaints, and production issues.
Provide motivation for employees, increasing morale, worker efficiency, and production rates.
Process and approve hourly timesheets and correct exceptions in a timely manner.
Monitor and assess employee’s performance, attendance, scheduling etc.
Ensure that work orders are completed in a timely fashion and within budget.
Ensure safety is a priority with all workers, oversee strict adherence to Alberta and Canadian Occupational Health and Safety guidelines, attend JHSA meetings as needed.
Work with other supervisors to coordinate operations and activities within and between departments
Demonstrate equipment operations and work and safety procedures to new employees or assign employees to experienced workers for training.
Read and analyze charts, work orders, production schedules and other records / reports to determine production requirements and to evaluate current production estimates and outputs and take action to meet schedule deadlines.
Read and review of manufacturing engineering packages and provide improvement feedback.
Performs all duties in accordance with Johnson Controls/Silent-Aire Limited Partnership safety program standards and Alberta Occupational Health and Safety Act, Regulations, and Code.
Other duties as required.
What we look for
Required:
3+ years’ experience as a production supervisor
Direct working knowledge of operations, warehouse, and transportation management
Knowledge of supplies, equipment, and/or services ordering, as well as inventory control of these items
Knowledge of local and federal regulations including AOHS and Employment Standards Code
Excellent analytical and problem-solving skills
Strong written and verbal skills to communicate with all levels of the organization and its executive team
Strong customer service orientation
Experience with all safe practices, procedures, and overall processes associated with manufacturing from raw materials to finished product
Ability to maintain a high level of communication with both internal and external stakeholders, customers, contractors, and industry peers
Always adhere to safety policies (wear protective equipment)
Shift hours are on a rotating schedule
Preferred:
University degree or diploma in related field
Training and knowledge of Six Sigma techniques, Kaizen, and Lean Manufacturing
First Aid skills and/or certificates
#LI-CC4
#LI-Onsite
Johnson Controls’ Canadian subsidiaries are committed to providing reasonable accommodation to applicants, candidates and employees with disabilities, in accordance with applicable human rights legislation, and in Ontario, in accordance with the Accessibility for Ontarians with Disabilities Act (“AODA”). When requested, accommodation will be provided throughout all stages of the recruitment and selection process. To request accommodation, please contact us. Any information you provide related to accommodation measures will be treated as confidential. A copy of Johnson Controls’ applicable AODA policies are available on our website at www.johnsoncontrols.com for your reference, and can be made available in accessible formats upon request.
Official account of Jobstore.
At Niagara, we’re looking for Team Members who want to be part of achieving our mission to provide our customers the highest quality most affordable bottled water.
Consider applying here, if you want to:
We offer competitive compensation and benefits packages for our Team Members.
Production OperatorThis position is responsible for daily operations of the production floor; ensuring the shift meets established safety, quality, and production goals in compliance with all applicable legal and food safety requirements.Essential Functions
Qualifications
*experience may include a combination of work experience and education
*experience may include a combination of work experience and education
Competencies
This position embodies the values of Niagara’s LIFE competency model, focusing on the following key drivers of success:
Education
Certification/License:
Foreign Language
Benefits
https://careers.niagarawater.com/us/en/benefits
Any employment agency, person or entity that submits a résumé into this career site or to a hiring manager does so with the understanding that the applicant's résumé will become the property of Niagara Bottling, LLC. Niagara Bottling, LLC will have the right to hire that applicant at its discretion without any fee owed to the submitting employment agency, person or entity.
Employment agencies that have fee agreements with Niagara Bottling, LLC and have been engaged on a search shall submit résumé to the designated Niagara Bottling, LLC recruiter or, upon authorization, submit résumé into this career site to be eligible for placement fees.
Official account of Jobstore.
Referred applicants should not apply directly to this role.
All referred applicants must first be submitted through Workday by a current Loblaw Colleague.
Founded in 2006, Joe Fresh is a leading source for modern style and accessible design, offering comprehensive lifestyle collections for men, women and children. Joe Fresh delivers quality and compelling value in categories spanning in apparel, accessories, and footwear. Joe Fresh collections are polished and sophisticated, with a focus on essential designs that appeal to a broad range of style-savvy consumers. With more than 350 Joe Fresh departments from coast to coast, the Joe fresh network is more than a great place to shop, it’s a great place to work. We’re committed to building our talented team who champion collaboration, kindness, and inclusivity. We are looking for innovative, hardworking, and collaborative team members for our Joe Fresh team. Join our team in our goal of helping Canadians Live Life Well®.
In addition, we believe that compliance with laws is about doing the right thing. Upholding the law is part of our Code of Conduct – it reinforces what our customers and stakeholders expect of us.
What you'll do:
Handle daily operation of a team of managers in ensuring smooth and timely execution of all Joe Fresh import orders.
Identify issues and ensure resolutions conducted in a timely manner. Make certain that all production related queries across internal and external partners are timely and properly address to.
Exercise sound judgement and critical thinking through problem resolution and setting of work/process guidelines to address any production follow-up issue.
Plan production organizational activities by establishing tasks, objectives and priorities. Balance workload distribution across the team and ensure appropriate support is established.
Disseminate/communicate production related corporate policies, processes and updates to internal and external partners as required by the business.
Work closely with internal partners to implement brand production initiatives and attend all critical meetings pertinent to production department.
Supervise personnel activity including hiring, training, and development of all subordinates to achieve department objectives and individual career goals performance including management of critical subordinate issues.
Review, evaluate, develop, and implement business procedures and policies to improve efficiency across the performance of the production team.
Collaborates with Supply Chain and Finance partners to mitigate risk and address all issues for on time delivery of all import orders.
Build relationships with both internal and external partners to foster a collaborative work environment and sustain long term alliances.
Provide accurate reports and detailed analysis on business deliverance.
Completes other tasks and assignments as required by management and aligns with Joe Fresh policies and procedures.
Building and leading diverse teams that foster a workplace of inclusiveness and belonging
What you bring:
Equivalent of a post-secondary diploma/degree combined with minimum 7 years in a supervisory experience preferably in sourcing/manufacturing/supply chain management within the fashion retail/ wholesale or garment manufacturing.
Well versed with Microsoft office applications.
Exceptional interpersonal, communication, negotiation and strong time management skills.
Well-developed organizational skills with ability to set and adjust to changing priorities, multi task and perform under deadline pressures in a fast-paced environment.
Reliable, responsible individual with strong work ethic, friendly attitude and willingness to learn.
High level of self-management, responsiveness, creative problem-solving and adaptability skills.
Analytical and highly collaborative.
How You’ll Succeed:
At Joe Fresh, we seek great people to continually strengthen our culture. We believe great people model our values, are authentic, build trust and make connections.
If that sounds like you, and you are open-minded, responsive to change and up to the challenges provided in a fast-paced retail environment, apply today.
Joe Fresh recognizes Canada's diversity as a source of national pride and strength. We have made it a priority to reflect our nation’s evolving diversity in the products we sell, the people we hire, and the culture we create in our organization. Accommodation is available upon request for applicants with disabilities in the recruitment and assessment process and when hired.
Official account of Jobstore.
The Role
Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.
Moderna's strategic partnership with the UK Government is exemplified by our innovative presence at Harwell. Our mission is to establish a leading-edge research, development, and manufacturing facility part of a long-term commitment to onshore mRNA vaccine production for respiratory diseases. This initiative will create a multitude of highly skilled jobs and foster collaboration with academic and NHS partners across the UK. We're looking for global experts eager to join us in this endeavor, contributing to a future where access to life-saving vaccines is a reality for all.
The Site Compliance Head at Moderna’s Harwell, UK site plays a pivotal role in implementing world-class quality system processes and operations. This leadership position is responsible for ensuring the highest level of compliance, providing strategic direction for the application of Moderna’s Quality Management System (QMS) in support of internal manufacturing of commercially registered products. The role involves assessing and monitoring the health of the QMS for continuous improvement, leading cross-functionally to maintain a state of inspection readiness, and building a culture of quality across the site.
Here’s What You’ll Do
Your key responsibilities will be:
Implementing Moderna’s overall Quality Management System (QMS), quality manual, policies, and procedures at the site.
Serving as a cross-functional quality leader and a GXP compliance subject matter expert.
Overseeing the performance and effectiveness of QMS programs, including Quality Risk Management, Training, Documentation and Records Management, and Data Integrity.
Maintaining the site in a constant state of inspection readiness, hosting inspections, and engaging directly with Health Authority inspectors.
Evaluating business goals, identifying improvement opportunities, and applying problem-solving techniques to improve product quality and process effectiveness.
Your responsibilities will also include:
Leading Management review meetings and monitoring the state of control of Moderna’s QMS at the site.
Serving as the site compliance representative on Global Compliance Councils.
Working collaboratively with the Compliance organizations across Global and the sites, along with the digital team, to drive effective and efficient processes supported with digital e-systems.
The key Moderna Mindsets you’ll need to succeed in the role:
We behave like owners: Taking ownership of the quality and compliance of our Harwell site, ensuring that every action reflects our commitment to excellence.
We pivot fearlessly: Embracing the dynamic nature of compliance and quality management, ready to adapt and respond to new data or regulations to maintain our high standards.
Here’s What You’ll Bring to the Table:
Bachelor degree, preferably in Sciences or Engineering
Applied Quality industry experience of 10+ years.
Demonstrated experience with Pharmaceutical Quality Systems.
Inspection experience preferred.
Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.
We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:
The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Moderna is a smoke-free, alcohol-free and drug-free work environment.
Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com. (EEO/AAP Employer)
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About Abbott Production Line Lead I
Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:
The Opportunity
This position works out of our Alajuela location. As the Production Line Lead I, your role is to assist the Production Supervisor in managing the daily activities of the production of ABBOTT products. Using his/her knowledge of the quality system, people management skills, and company policies and procedures, the Production Leader ensures that procedures are followed, non-conformance issues are elevated immediately, and that staff is performing at expected levels.
What You’ll Do
Required Qualifications
SHIFT B (Monday to Friday 3:30 pm to 10:00 pm and Saturdays 8:00 am to 3:30 pm)
Preferred Qualifications
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.
The base pay for this position is
N/A/hourIn specific locations, the pay range may vary from the range posted.
Official account of Jobstore.
About Abbott
Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:
The Opportunity
This position works out of our Alajuela, Zona Franca Coyol location in EP Business. In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.
What You’ll Do
This position executes Documentation Control activities which includes:
Supports supervisor optimizing the resources within the shift to achieve key indicator goals as Safety, Quality, line output, yield and productivity rates, among others.
• Assure the production schedule adherence for his/her area providing support to the direct labor personnel. Communicate results or deviations of the production schedule to the supervisor in a timely manner.
• Collaborate with the supervisor on administrative task as vacations coordination, direct labor attendance, personnel transportation, among others.
• Assure the manufacturing process is followed, documentation is filled out and the product is properly handled as to avoid any quality issues or discrepancies.
• Provides feedback to the supervisor related to personnel performance. Supports the supervisor providing continued feedback to direct labor, reinforcing and recognizing the desired behavior and confront the unaccepted behavior. Assure the company principles and policies are consistently followed.
• Might be responsible to keep track of the line metrics and report results on a daily basis.
• Additional to the normal duties should be capable to partially cover the supervisor responsibilities if needed taking people, safety and quality decisions as needed
• Supports the supervisor to control and or execute documentation tasks of production records as applicable.
Required Qualifications
Must have high school degree, Supervision, Engineering or similar career.
3-5 years’ experience as team member/trainer, technician or similar position in a complex manufacturing environment. (Medical Industry preferred).
Demonstrated knowledge of quality systems, production metrics, and inventory control methods.
Demonstrated computer skills and basic MS Office knowledge.
Demonstrate proficiency in technical aspects of the position to achieve a high level of performance. For example proficiency controlling production indicators, SAP, Windchill, or other systems utilized on the manufacturing environment.
Demonstrated capacity to lead/manage people.
Preferred Qualifications
Basic knowledge of English)
Desirable previous supervision/leader experience in Medical devices / Technological manufacturing environment, or proven experience leading direct labor personnel.
SHIFT TB
The base pay for this position is
N/A/hourIn specific locations, the pay range may vary from the range posted.
Official account of Jobstore.
*We are excited to announce that we are expanding our team and have multiple positions available for this role - join us in shaping the future!*
The Role:
Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.
Moderna's strategic partnership with the UK Government is exemplified by our innovative presence at Harwell. Our mission is to establish a leading-edge research, development, and manufacturing facility part of a long-term commitment to onshore mRNA vaccine production for respiratory diseases. This initiative will create a multitude of highly skilled jobs and foster collaboration with academic and NHS partners across the UK. We're looking for global experts eager to join us in this endeavour, contributing to a future where access to life-saving vaccines is a reality for all.
Reporting to the Quality Control Associate Director, the individual in this role will perform cGMP QC testing for QC Chemistry, release, and stability. You will also be responsible for supporting Global GMP stability programs, stability sample set down, pull, and sample shipment/receipt activities. Additionally, the individual in this role will be involved in routinely maintaining of stability databases, performing data trending and statistical analyses, creation, revision, review and approval of SOP’s, stability protocols and stability reports in accordance with current GMP, FDA, EU and ICH guidelines and regulations; this individual may support special projects as assigned.
Here’s What You’ll Do:
Your key responsibilities will be:
Performing routine analytical chemistry & stability testing, including HPLC, UPLC, GC, UV, Particle Analysis by Dynamic Light Scattering, KF, etc.
Supporting Global GMP stability programs, stability sample set down, pull, and sample shipment/receipt activities.
Maintaining stability databases, performing data trending and statistical analyses.
Creating, revising, reviewing, and approving SOPs, stability protocols, and reports in line with GMP, FDA, EU, and ICH guidelines.
Your responsibilities will also include:
LIMS sample result entry, execution of Electronic Assay Forms in LIMS.
General laboratory support activities, including reagent preparation, sample management, and equipment maintenance.
Establishing and maintaining a safe laboratory working environment.
Supporting and executing stability sample shipments to external labs, and updating in-house stability databases.
The key Moderna Mindsets you’ll need to succeed in the role:
Pivot Fearlessly: You will navigate through the complexities of QC testing and stability studies, adapting to new challenges and data with agility.
Pursue Options in Parallel: Your role demands managing multiple stability protocols and analytical methods simultaneously to ensure the most efficient outcomes.
Here’s What You’ll Bring to the Table:
BA/BSc in Chemistry (preferred) or other relevant scientific discipline.
Working experience: at least 5-7 years in quality control laboratory of a pharmaceutical company.
Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.
We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:
The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Moderna is a smoke-free, alcohol-free and drug-free work environment.
Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com. (EEO/AAP Employer)
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Official account of Jobstore.
The Role:
Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization, working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.
Moderna's strategic partnership with the UK Government is exemplified by our innovative presence at Harwell. Our mission is to establish a leading-edge research, development, and manufacturing facility part of a long-term commitment to onshore mRNA vaccine production for respiratory diseases. This initiative will create a multitude of highly skilled jobs and foster collaboration with academic and NHS partners across the UK. We're looking for global experts eager to join us in this endeavor, contributing to a future where access to life-saving vaccines is a reality for all.
As the Microbiology & Bioassay Quality Control Analyst at Moderna, you will embark on a transformative journey, reporting directly to the Associate Director of Quality Control. In this pivotal role, you'll perform critical Quality Control testing using cutting-edge Bioassay and Microbiology techniques within a GMP testing environment, supporting mRNA product production at Moderna’s manufacturing facility and affiliated organizations. Your work will encompass a broad range of microbiological and molecular biology methods, including but not limited to Bioburden, Sterility, BET, Micro sequencing, Agarose Gel Electrophoresis, UV/Vis measurement, Sanger Sequencing, protein concentration determination, qPCR, ELISA, and Cell-Based Potency testing. This role is instrumental in ensuring the highest quality of mRNA products, contributing to Moderna's mission of delivering the greatest possible impact to people through innovative mRNA medicines.
Here’s What You’ll Do:
Your key responsibilities will be:
Executing GMP QC Molecular Biology and Microbiology methods.
Supporting drug substances and drug products testing.
Conducting analysis related to Bioassay and Microbiology laboratory.
Participating in method transfers and qualification activities.
Assisting in the development, implementation, and maintenance of laboratory operational systems in accordance with cGMP requirements.
Your responsibilities will also include:
Providing support to audit teams.
Preparing and managing contract laboratory testing samples.
Performing general laboratory support activities.
Participating in equipment and method qualifications, validations, and method transfers.
Participating in authoring quality systems records and writing/revising SOPs, protocols, and reports.
The key Moderna Mindsets you’ll need to succeed in the role:
Pivot Fearlessly: This role requires adaptability and resilience, embracing change and new methodologies to ensure quality and efficiency in QC testing.
Pursue Options in Parallel: A strategic mindset to explore and implement various testing methodologies simultaneously, optimizing for the best outcomes in quality control processes
Here’s What You’ll Bring to the Table:
BSc/BA in a relevant scientific discipline with 5-7 years Quality Control experience in a cGMP organization with a focus in Molecular Biology, DNA Sequencing and Microbiology.
Hands on experience with molecular biology techniques including, but not limited to, gel electrophoresis, qPCR, and Sanger Sequencing.
Hands-on experience of various Microbiology testing techniques and analyses (e.g. Vitek, Isolator Technology, Bioburden, BET, Sterility, others)
Working knowledge of relevant and current FDA, EU, ICH guidelines and regulations preferred.
Working experience in a GMP environment.
Ability to collaborate effectively in a dynamic, cross-functional matrix environment.
Ability to efficiently prioritize and complete multiple projects and tasks in a fast-paced environment.
Proven ability to conduct investigations.
Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.
We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:
The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Moderna is a smoke-free, alcohol-free and drug-free work environment.
Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com. (EEO/AAP Employer)
-
Official account of Jobstore.
The Role:
Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.
Moderna's strategic partnership with the UK Government is exemplified by our innovative presence at Harwell. Our mission is to establish a leading-edge research, development, and manufacturing facility part of a long-term commitment to onshore mRNA vaccine production for respiratory diseases. This initiative will create a multitude of highly skilled jobs and foster collaboration with academic and NHS partners across the UK. We're looking for global experts eager to join us in this endeavour, contributing to a future where access to life-saving vaccines is a reality for all.
Reporting to the Quality Control Associate Director, the individual in this role will perform cGMP QC testing for QC Chemistry, release, and stability. You will also be responsible for supporting Global GMP stability programs, stability sample set down, pull, and sample shipment/receipt activities. Additionally, the individual in this role will be involved in routinely maintaining of stability databases, performing data trending and statistical analyses, creation, revision, review and approval of SOP’s, stability protocols and stability reports in accordance with current GMP, FDA, EU and ICH guidelines and regulations; this individual may support special projects as assigned.
Here’s What You’ll Do:
Your key responsibilities will be:
Performing routine analytical chemistry & stability testing, including HPLC, UPLC, GC, UV, Particle Analysis by Dynamic Light Scattering, KF, etc.
Supporting Global GMP stability programs, stability sample set down, pull, and sample shipment/receipt activities.
Maintaining stability databases, performing data trending and statistical analyses.
Creating, revising, reviewing, and approving SOPs, stability protocols, and reports in line with GMP, FDA, EU, and ICH guidelines.
Your responsibilities will also include:
LIMS sample result entry, execution of Electronic Assay Forms in LIMS.
General laboratory support activities, including reagent preparation, sample management, and equipment maintenance.
Establishing and maintaining a safe laboratory working environment.
Supporting and executing stability sample shipments to external labs, and updating in-house stability databases.
The key Moderna Mindsets you’ll need to succeed in the role:
Pivot Fearlessly: You will navigate through the complexities of QC testing and stability studies, adapting to new challenges and data with agility.
Pursue Options in Parallel: Your role demands managing multiple stability protocols and analytical methods simultaneously to ensure the most efficient outcomes.
Here’s What You’ll Bring to the Table:
BA/BSc in Chemistry (preferred) or other relevant scientific discipline.
Working experience: at least 5-7 years in quality control laboratory of a pharmaceutical company.
Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.
We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:
The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Moderna is a smoke-free, alcohol-free and drug-free work environment.
Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com. (EEO/AAP Employer)
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Official account of Jobstore.
The Role:
Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization, working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.
Moderna's strategic partnership with the UK Government is exemplified by our innovative presence at Harwell. Our mission is to establish a leading-edge research, development, and manufacturing facility part of a long-term commitment to onshore mRNA vaccine production for respiratory diseases. This initiative will create a multitude of highly skilled jobs and foster collaboration with academic and NHS partners across the UK. We're looking for global experts eager to join us in this endeavor, contributing to a future where access to life-saving vaccines is a reality for all.
As the Microbiology & Bioassay Quality Control Analyst at Moderna, you will embark on a transformative journey, reporting directly to the Associate Director of Quality Control. In this pivotal role, you'll perform critical Quality Control testing using cutting-edge Bioassay and Microbiology techniques within a GMP testing environment, supporting mRNA product production at Moderna’s manufacturing facility and affiliated organizations. Your work will encompass a broad range of microbiological and molecular biology methods, including but not limited to Bioburden, Sterility, BET, Micro sequencing, Agarose Gel Electrophoresis, UV/Vis measurement, Sanger Sequencing, protein concentration determination, qPCR, ELISA, and Cell-Based Potency testing. This role is instrumental in ensuring the highest quality of mRNA products, contributing to Moderna's mission of delivering the greatest possible impact to people through innovative mRNA medicines.
Here’s What You’ll Do:
Your key responsibilities will be:
Executing GMP QC Molecular Biology and Microbiology methods.
Supporting drug substances and drug products testing.
Conducting analysis related to Bioassay and Microbiology laboratory.
Participating in method transfers and qualification activities.
Assisting in the development, implementation, and maintenance of laboratory operational systems in accordance with cGMP requirements.
Your responsibilities will also include:
Providing support to audit teams.
Preparing and managing contract laboratory testing samples.
Performing general laboratory support activities.
Participating in equipment and method qualifications, validations, and method transfers.
Participating in authoring quality systems records and writing/revising SOPs, protocols, and reports.
The key Moderna Mindsets you’ll need to succeed in the role:
Pivot Fearlessly: This role requires adaptability and resilience, embracing change and new methodologies to ensure quality and efficiency in QC testing.
Pursue Options in Parallel: A strategic mindset to explore and implement various testing methodologies simultaneously, optimizing for the best outcomes in quality control processes
Here’s What You’ll Bring to the Table:
BSc/BA in a relevant scientific discipline with 5-7 years Quality Control experience in a cGMP organization with a focus in Molecular Biology, DNA Sequencing and Microbiology.
Hands on experience with molecular biology techniques including, but not limited to, gel electrophoresis, qPCR, and Sanger Sequencing.
Hands-on experience of various Microbiology testing techniques and analyses (e.g. Vitek, Isolator Technology, Bioburden, BET, Sterility, others)
Working knowledge of relevant and current FDA, EU, ICH guidelines and regulations preferred.
Working experience in a GMP environment.
Ability to collaborate effectively in a dynamic, cross-functional matrix environment.
Ability to efficiently prioritize and complete multiple projects and tasks in a fast-paced environment.
Proven ability to conduct investigations.
Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.
We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:
The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Moderna is a smoke-free, alcohol-free and drug-free work environment.
Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com. (EEO/AAP Employer)
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Official account of Jobstore.
At Niagara, we’re looking for Team Members who want to be part of achieving our mission to provide our customers the highest quality most affordable bottled water.
Consider applying here, if you want to:
We offer competitive compensation and benefits packages for our Team Members.
Aseptic Production Operator IIAs an Aseptic Production Operator II, your primary responsibility is to ensure the safe, efficient, and compliant operation of aseptic manufacturing processes and equipment. You will focus mostly on the Aseptic Block Equipment (Blowmolder, Filler, and its peripherals devices). You will play a crucial role in maintaining sterile conditions and producing high-quality beverage products. As a senior production team member, you will also provide junior operators guidance, training, and support.Key Responsibilities
Please note that this job description is not designed to contain a comprehensive list of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time, with or without prior notice.
Qualifications
*Experience may include a combination of work experience and education
*Experience may include a combination of work experience and education
Competencies
This position embodies the values of Niagara’s LIFE competency model, focusing on the following key drivers of success:
Education
Microbiology, Chemistry, or Engineering.
Certification/License
Foreign Language
Benefits
https://careers.niagarawater.com/us/en/benefits
Any employment agency, person or entity that submits a résumé into this career site or to a hiring manager does so with the understanding that the applicant's résumé will become the property of Niagara Bottling, LLC. Niagara Bottling, LLC will have the right to hire that applicant at its discretion without any fee owed to the submitting employment agency, person or entity.
Employment agencies that have fee agreements with Niagara Bottling, LLC and have been engaged on a search shall submit résumé to the designated Niagara Bottling, LLC recruiter or, upon authorization, submit résumé into this career site to be eligible for placement fees.
Official account of Jobstore.
We are currently looking for a talented manufacturing engineer to oversee and improve manufacturing processes for our Switchgear & Automatic Transfer Switch facilities in Apodaca, Mexico.
The manufacturing engineer will serve as a key member of the Operations and Engineering teams. A successful candidate will need to be able to work effectively within a team and have a high level of technical expertise. As part of this role, they will be developing and optimizing manufacturing processes to improve efficiency, productivity, cost, and quality.
Major Responsibilities:
Required Education, Experience and Skills:
Regal Rexnord Corporation (“Regal Rexnord”) is a leading manufacturer of electric motors, electrical motion controls, power generation and mechanical power transmission products and sub-systems, serving customers around the world in the general industrial, consumer, commercial construction, food & beverage, and alternative energy end markets, among others. Regal Rexnord sells its products and solutions to OEMs, through distributors, and directly to end-users. Regal Rexnord is a $7.2B company with 36,000 associates globally.
You may not know it, but Regal Rexnord impacts your life every day. The company’s products enable the fans in HVAC systems that keep us comfortable; the power source that keeps smart buildings running; the agricultural and food service equipment that keeps us fed; and the conveyer systems that keep e-commerce flowing, to name a few of the applications where our products are used.
Regal Rexnord’s business purpose is to create a better tomorrow by energy-efficiently converting power into motion. This means creating innovative solutions while focusing on both customer needs and the company’s commitment to sustainability. The company’s industrial powertrain and automation solutions offerings are an important part of the company's growth strategy. The company’s strategy includes leveraging 80/20 to prioritize all activities, including product excellence, operational excellence and commercial excellence (i) driving organic sales growth through the introduction of innovative new products, with a particular focus on improving energy efficiency, (ii) establishing and maintaining new customers, as well as developing new opportunities with existing customers, (iii) participating in higher growth end markets and geographies, and (iv) identifying and consummating strategic, value creating acquisitions.
Official account of Jobstore.
The Role:
Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.
Moderna's strategic partnership with the UK Government is exemplified by our innovative presence at Harwell. Our mission is to establish a leading-edge research, development, and manufacturing facility as part of a long-term commitment to onshore mRNA vaccine production for respiratory diseases. This initiative will create a multitude of highly skilled jobs and foster collaboration with academic and NHS partners across the UK. We're looking for global experts eager to join us in this endeavor, contributing to a future where access to life-saving vaccines is a reality for all.
We are seeking a Quality Assurance Specialist for real-time quality oversight of internal manufacturing at Moderna Inc., located at our Harwell, UK site. This role involves being part of a cohesive team responsible for supporting cGMP mRNA drug substance production internally. The successful candidate will work cross-functionally with Operations, Manufacturing Science and Technology, and other departments, providing real-time quality oversight and expertise to ensure technical success with strict adherence to the Quality System. This position requires strong decision-making skills, independent thinking, and the ability to make or escalate decisions regarding operations as needed.
Here’s What You’ll Do:
Your key responsibilities will be:
Providing on-the-floor Quality support to Manufacturing, including real-time observation of activities and monitoring process operations to ensure compliance with specifications.
Making quality decisions and/or escalating issues to management that may impact operations, identifying risks, and communicating gaps for quality and GMP process/systems.
Performing routine walkthroughs of the manufacturing suites to ensure appropriate suite maintenance, implementation of GMP best practices, and troubleshooting when problems arise.
Enforcing adherence to cGMPs, SOPs, and manufacturing documentation.
Partnering with manufacturing and support teams to initiate and triage new deviation events, reviewing minor manufacturing deviations.
Authoring and reviewing documentation, including SOPs and WIs, to ensure compliance and adherence to regulations/cGMP operations, and reviewing executed electronic and paper batch record documentation.
Practicing safe work habits and adhering to Moderna’s safety procedures and guidelines.
Utilizing knowledge to improve operational efficiency.
Operating on a shift structure.
Your responsibilities will also include:
Engaging in continuous learning and development related to quality assurance, cGMP practices, and operational efficiency.
The key Moderna Mindsets you’ll need to succeed in the role:
We push past possible: Demonstrating a relentless pursuit of innovation and operational excellence in quality assurance.
We pivot fearlessly: Adapting quickly to operational challenges and changes in manufacturing processes with a solutions-oriented approach.
Here’s What You’ll Bring to the Table:
Bachelor’s Degree in a science field (e.g., Biology, Microbiology, Chemistry, Pharmacy, Engineering) or equivalent combination of education and experience
3 – 5 years of pharmaceutical or related work experience with emphasis on current Good Manufacturing Practices
Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.
We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:
The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Moderna is a smoke-free, alcohol-free and drug-free work environment.
Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com. (EEO/AAP Employer)
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Official account of Jobstore.
Manufacturing jobs are involved in developing new products with raw materials or components. These jobs are located in a factory, plant or mill. Manufacturing and production are comprised of technicians, production manager, production planner, production supervisor, assembler, operators, assemblers, machinists, fabricators, printing, quality control, tailors, welders, water treatment and woodworkers.
The role of welder is to cut and join metals at facilities. Responsibilities include reading measurements to plan layout, determine the appropriate welding equipment, set up components for welding according to specifications, align components using clamp pieces, repair machinery, inspecting welded structure to find flaws and maintain equipment in a condition that does not compromise safety.
The role of production engineer is to oversee the production of goods in various industries at factories. Responsibilities include handling budget, ensuring project deadlines are met, analysis of the data found in charts, analysis of operational issues, provide team with technical support and training.
The role of production manager is to organise and oversee the manufacturing of goods. Responsibilities include liaising with other managers to formulate objectives, prepare budgets, organise workflow to meet specifications, monitor production to resolve issues, evaluate the performance of production personnel, approve maintenance work, enforce health and safety regulations.
The role of production planner is to organise production according to demand and quality standards. Responsibilities include plan operations to ensure maximum performance, assign workers to particular production operations, schedule shift according to production needs, monitor jobs to ensure they will finish on time, address issues when they arise aiming for minimum disruption and keep paperwork organised.
The role of operator is to set up, maintain and operate machinery. Responsibilities include feed raw material to semi-automated machines, inspect parts with precision, test operations of machines periodically, fix issues that might occur during the shift, check output to spot any machine-related mistakes, keep records of products and maintain activity logs.
The role of maintenance technician is to manage maintenance in the facilities to ensure the smooth running of upkeep or repair operations, Responsibilities include inspect facilities periodically to determine problems, prepare weekly maintenance schedules, recruit maintenance technicians, supervise tradesmen during installations,ensure adherence to quality standards, health and safety regulations.
The role of technician is to deliver the desired customer service experience. Responsibilities include providing customer support during field visits, tie workflow to schedule, manage all on site installations, diagnose technical problems, produce detailed service reports, document process, follow all company’s filed procedures and protocols.
The role of OSH officer is to facilitate compliance with occupational health and safety(OHS) guidelines. Responsibilities include supporting the development of OHS policies, advise on various safety-related topics, conduct a risk assessment, review existing policies, organise OHS training of employees, prepare reports on occurrences and provide statistical information to upper management.
The role R&D engineer is to conduct research and development activities for an organisation. Responsibilities include summarise research results, assess the scope of research projects, ensure projects are within budget, develop technical documentation for all projects, take leadership of projects in development, collaborate with engineers and developers to create product designs with marketing teams to develop sales plans for future products.
The role of boilerman is to maintain heating systems in large buildings in the boiler, engine and mechanical rooms. Responsibilities include handling hot water heating systems, perform routine maintenance, keeping safety at the forefront when attending to problems, record service data in logs and follow strict safety procedures during work.
The role of CNC machinist is to use computer numerically controlled(CNC) machinery safely and accurately to perform a variety of functions. Responsibilities include understand specifications of the task at hand, translate instructions into cnc programming so the machines can perform the correct function, prepare raw materials, prepare test runs for cnc mills and maintain machinery daily to ensure functionality.
The role of machine operator is to set up, maintain and operate machinery. Responsibilities include set up machines to start a production cycle, adjust machine settings, feed materials to semi-automated machines, test operations of machines periodically, fix issues that might occur during the shift, check output to spot any machine-related flaws and maintain activity logs.
The role of storekeeper is to manage the maintenance of a department’s storeroom which includes stocking of operational materials and supplies. Responsibilities include keeping records to maintain inventory control, oversees mail handling, operate simple office machines, perform related and peripheral site-specific duties as required.