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Why Lineage?
This is an excellent position to begin your career path within Lineage! Success in this role enables greater responsibilities and promotions! A career at Lineage starts with learning about our business and how each team member plays a part each and every day to satisfy our customers’ requirements. Beyond that, you’ll help us grow and learn on our journey to be the very best employer in our industry. We’ll ask you for your opinion and ensure we do our part to keep you developing and engaged as we grow our business. Working at Lineage is energizing and enjoyable. We value respect and care about our team members.
Lineage is an Equal Employment Opportunity Employer and is committed to compliance with all federal, state, and local laws that prohibit workplace discrimination and unlawful harassment and retaliation. Lineage will not discriminate against any applicant on the basis of race, color, age, national origin, religion, physical or mental disability or any other protected status under federal, state and local law.
Benefits
Lineage provides safe, stable, reliable work environments, medical, dental, and basic life and disability insurance benefits, 401k retirement plan, paid time off, annual bonus eligibility, and a minimum of 7 holidays throughout the calendar year.
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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’ll also have access to:
The Opportunity
This position works out of our Alameda, CA location in the Diabetes Care division. We’re focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology.
The Supplier QA Engineer II supports in the evaluation, selection, approval and maintenance of the division's approved suppliers by performing supplier quality system assessments, monitoring supplier performance, and driving supplier corrective action and/or improvement activities.
What You’ll Work On
Ensures that the division’s approved supplier list is maintained and accurate.
Assesses potential new suppliers and service providers for quality and quality system capabilities through the execution of on-site or desk top audits, and review of other objective evidence, as required.
Communicates division’s approval requirements to supplier and monitors feedback per project timelines.
Performs on-site quality assessments of new suppliers, as required, and ensures appropriate corrective action response to findings.
Ensures Document Control is notified of any changes to supplier statuses, as they relate to the Agile Manufacturer’s Tab.
Ensures that the supplier performs and documents the appropriate engineering approach to activities such as qualification and validation and provides assistance in these efforts, as appropriate.
Leads in the evaluation and approval of supplier requested changes or improvements. This activity may also include the identification and/or approval of a new supplier to provide an alternate material.
Conducts site visits at supplier sites to bring back understanding on how to resolve quality issues (process audits).
Evaluates Exception Reports (ERs) issued for nonconforming supplied material and works with the supplier on the investigation and resolution of root cause issues.
Notifies suppliers of customer complaints related to failures resulting from supplied material and requires investigation and corrective action.
Monitors supplier performance and reports supplier quality trend data. Drives improvement projects, as required, to improve supplier performance.
Assists in the preparation of area metric data for delivery to Sr. Management. Recommends areas for supplier improvement, as appropriate.
Participates with Incoming Quality Control on the development of incoming inspection activities or the reduction of these activities through implementation and maintenance of the Material Certification Program.
Responsible for approving First Article Inspections and/or Golden Samples, as initiated by suppliers.
Required Qualifications
Bachelor’s degree or an equivalent combination of education and work experience
Minimum 6 years of Quality Assurance experience in the medical device, pharmaceutical or other quality managed industries
Preferred Qualifications
Some working knowledge of applicable regulations such as FDA, QSR, ISO, MDD, or IVDD
Some knowledge in the areas of design controls, verification and validation activities, manufacturing practices and statistical techniques.
Some experience in conducting external quality assessments.
Certified Lead Auditor trained
Proficient in MS Office (Word, Excel, Outlook)
Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization
* Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
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 and @AbbottGlobal.
The base pay for this position is
$83,600.00 – $167,200.00In specific locations, the pay range may vary from the range posted.
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
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Pfizer Singapore is recruiting employees for manufacturing site expansion of PFIZER ASIA MANUFACTURING PTE LTD (PAMPL) in Singapore.
Why Patients Need You
Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.
What You Will Achieve
You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. Your knowledge of quality control will be helpful to support our quality programs. Your ability to analyze chemical, biological or microbiological products will help us manage our quality. Your contribution to environmental testing, utility monitoring, analytical testing, microbial identification and sterility testing will help Pfizer provide safe drugs to its patients.
Your qualifications of unique Quality Control instruments will help us meet accuracy specifications for sample management, retains managements, interpretation and evaluation. You will also be relied on for establishing requirements for the transfer of methodology from R&D.
As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.
It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
Qualifications
Position Summary:
The incumbent is a member of the Quality Control (QC) Laboratory Systems team. Under the supervision of the QC Manager / Supervisor (Systems team), the key responsibilities are:
· Perform / review and document analytical testing and results accurately and in accordance to test methods, site SOPs and relevant protocols, adhering to ALCOA principles and Data Integrity (DI) requirements.
· Assist in troubleshooting laboratory technical problems and support laboratory investigations.
· Author SOPs, analytical method transfer protocols and reports and other GMP documentation (e.g. trend reports).
· Perform preventive maintenance or calibration of instrumentation as required, undertake housekeeping responsibilities and follow safety regulations.
· Set up and maintain QC processes (e.g. reference standard and retention samples management)
· Use Imex "way of working" for day to day operations, problem solving, escalation and continuous improvements.
Responsibilities:
· Perform / review and document analytical testing and results accurately and in accordance to test methods, site SOPs and relevant protocols, adhering to ALCOA principles and Data Integrity (DI) requirements.
· Perform / review and document equipment verification and calibration in accordance to procedures.
· Highlight any abnormalities detected during testing / review and raise laboratory investigations as required.
· Support laboratory investigations and perform equipment troubleshooting where required.
· Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures are followed.
· Author SOPs, analytical method transfer protocols and reports and other GMP documentation (e.g. trend reports).
· Set up and maintain QC processes (e.g. reference standards and retention sample management), perform investigations as required for any associated deviations.
· Conduct training for fellow colleagues from QC and other departments (e.g. Production).
· Uphold Pfizer's code of conduct and values.
· Collaborate with cross-functional teams to drive flawless execution.
· Play an active and impactful role in Tier processes by updating performance against metrics, highlighting issues, with appropriate escalations. Support development and implementation of solutions.
· Contribute to the continuous improvement activities in QC laboratory or cross functional teams as nominated.
Job Related Requirements:
· Effective problem solving skills.
· Demonstrated ability to perform in a team.
· Knowledge of cGMPs and ALOCA principles.
· Possess a can-do/pride to succeed attitude.
· Embrace the use of digital technology to scale and speed up every form of interaction and action.
Must-Have
· Bachelor's Degree in Science
· Demonstrated technical skills in method validation and testing
· Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations
· Knowledge of Good Manufacturing Practices and its application standards, processes and policies
· Excellent organizational skills and strong ability to multi-task
· Strong written and verbal communication skills
Nice-to-Have
· A minimum of 1 year QC experience in an analytical laboratory is preferred.
· Laboratory work experience with analytical HPLC (High Pressure Liquid Chromotography) Technique
· Experience leading continuous improvement projects
· Knowledge of lean manufacturing, six sigma methodologies, and statistics
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Quality Assurance and Control#LI-PFEOfficial account of Jobstore.
About the role
As our next Quality Assurance, you will get a chance to help our customer, by recommending improvements, and develop automation to scale our testing process. You will actively collaborate with Product Managers, Engineering, and DevOps to help Amartha to deliver innovative and delightful user experiences.
Responsibilities
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About Us
G Adventures is the world’s largest small-group adventure travel company and we’ve been making epic travel memories happen on all seven continents for over 30 years.
Our mission is simple: to change lives through travel. And not just our travelers’ either. Since day one, our tours have been built to establish meaningful relationships with local communities, directly benefiting the people and places we visit at every step of our tours.
With the demand for travel coming back strong, we are set up and excited for this next chapter in our company’s story — and we’d love for you to be a part of it.
Our DNA revolves around building, nurturing, and developing a diverse culture of people and a true sense of belonging, where everyone is encouraged to bring their authentic self to work each and every day. You’ll have the opportunity to grow your career, and yourself, alongside a passionate, talented, and welcoming community that works hard to spread goodness around the world.
If all that sounds like your kind of thing, well, we can’t wait for you to join us.
About the Role
Changing the world through travel: that’s been our goal since 1990. Sure, call us dreamers (wouldn’t be the first time), but that idea has been at the heart of everything we’ve ever done and has helped us grow into one of the biggest adventure travel companies on the planet.
Our developers are excited to work at G Adventures because we love tech, travel, and changing people's lives. We pride ourselves in working in an open-source environment with the ability to select the right tools for the job. Our industry, adventure travel, is fun and there are many challenges for curious software engineers, or even just slightly inquisitive ones.
You’ll be joining the Reservations Systems team within the amazing Technology department here at G. Your role will focused on helping to drive our reservation system, Compass, and related applications forward. Compass is used globally by our Sales, Operations, and Finance teams and continues to evolve as we expand and modernize it.
We believe that embracing our unique perspectives and expertise is key to our success as a collaborative team. We are seeking product-minded, empowered individuals who work collaboratively with their globally distributed peers on interesting problems. We value diversity, attracting the best people in the world to serve as colleagues.
What You'll be Doing
Learn all you can about our existing system and applications
Test software applications and systems
Write clean, efficient, and maintainable test cases
Debug and troubleshoot software defects and performance issues
Develop and implement comprehensive testing plans, including unit, integration, and system testing
Maintain accurate and up-to-date documentation of code, processes, and project-related information
Stay up-to-date with industry trends and emerging technologies
Desired Skills and Experience
2+ years of Python experience; Django is a plus
3+ years of automated testing experience
Comfortability learning a bit of JavaScript, if you don’t know it already
Ability to navigate the command line
Strong and demonstrated data modeling experience with attention to detail
SQL familiarity; you can hand code moderately complex SQL queries, but only when needed
Excellent communication skills, written and verbal
Ability to write documentation clearly and concisely, and to communicate well with non-technical stakeholders
Experience working closely with Web/REST/GraphQL APIs
Understanding of common application stacks (nginx, uwsgi, etc.)
Knowledge of web standards; excitement about new technologies
What do we offer you?
Competitive salary commensurate with the role
Competitive benefits package
Birthday day off
Vacation time for you to recharge
Enhanced Parental Leave
Learning and growth opportunities
*Applicable based on location*
G Adventures is an equal opportunity employer committed to fostering a diverse and inclusive work environment. We consider all qualified applicants.
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Primary City/State:
Tucson, ArizonaDepartment Name:
Quality Improvement-CorpWork Shift:
DayJob Category:
Risk, Quality and SafetyGreat careers are built at Banner Health. There’s more to health care than doctors and nurses. We support all staff members as they find the path that’s right for them. Apply today, this could be the perfect opportunity for you.
Becker’s Healthcare recently honored Banner as one of 150 top places to work in health care for 2023, we are proud to offer our team members many career and lifestyle choices throughout our network of facilities. At Banner Health, we’re excited about what the future holds for health care. That’s why we’re changing the industry to make the experience the best it can be. If you’re ready to change lives, we want to hear from you.
In this role you will be reviewing safety metrics and escalating issues, working to identify opportunities and provide recommendations and ideas.. Your work will include:
facilitating team projects
collecting and analyzing data
organizing and facilitating committee meeting and projects
This role is onsite and has the options of a 5, 8 hour shift schedule or an 80 hours in 9 days schedule with every other Friday off!
Your pay and benefits are important components of your journey at Banner Health. This opportunity includes the option to participate in a variety of health, financial, and security benefits.
POSITION SUMMARY
This position supports high reliability in clinical performance through ongoing assessment of performance, prioritizes clinical improvement activities, facilitates performance improvement, and promotes successful implementation to achieve entity/system targets. This role requires strong communication, collaboration, teamwork, and change management skills in order to achieve desired results across the continuum of care.
CORE FUNCTIONS
1. Quality Leadership and Integration - Facilitates the integration of quality into the fabric of the organization to achieve objectives, such as Annual Initiatives, Centers for Medicare and Medicaid Services (CMS) and The Joint Commission (tJC) standards of care. Support the quality infrastructure, protect the use of privileged or confidential information, facilitate processes for engagement and interprofessional teamwork, identify and promote continuous learning opportunities to advance the organization/facility/entity and communicate effectively. Facilitates performance improvement projects with physicians, clinical leaders, and staff to identify improvement opportunities utilizing qualitative and quantitative data analysis, knowledge of health care operations and systems thinking.
2. Performance and Process Improvement – Serves as a subject matter expert in performance and process improvement, project management and change management methods to support operational and clinical quality initiatives. Facilitates activities related to or resulting from patient safety, harm reduction, clinical performance, peer review and compliance with regulatory and accrediting agencies. This is accomplished by utilizing performance and process improvement tools and principles, applying project management methods, and using change management principles and tools.
3. Population Health and Care Transitions - Evaluate and improve healthcare processes and care transitions to advance the efficient, effective, and safe care of defined populations. Foster integrated team-based clinical delivery model to population-based care. Implement Clinical Practices, standardized process, that are evidence-based Population Health management strategies, encourage and contribute to a holistic approach to improvement and collaborate to improve care processes and transitions back to the community. Monitor and report facility Clinical Practice performance that have been handed-off to Quality Improvement.
4. Health Data Analytics - Supports the organizations' analytic environment to help guide data driven decision making while facilitating meetings with departments and teams to guide quality improvement initiatives and activities. Adheres to procedures for the confidentiality and integrity of data, designing, influencing, and monitoring data collection plans for Key Performance Indicators. Collaborates with process owner(s), acquiring, and integrating data from internal and external benchmarking sources. Uses statistical and visualization methods to analyze data for administrative and clinical decision making. Provides on-going assessment of performance, analyzes clinical outcome data, and identifies performance improvement opportunities or trends. Conducts and reports to stakeholders in-depth assessment of qualitative and quantitative data.
5. Patient Safety - Participates in and contributes to a safe healthcare environment by promoting safe practices, nurturing a just culture, and improving processes that detect, mitigate, or prevent harm. Seves as an advocate for the patient safety culture, applying safety science principles/methods, identify and report patient safety risks/events and collaborates to analyze patient safety risks and events. They facilitate teams to improve processes that impact the safety of patients.
6. Regulatory and Accreditation - Supports the evaluating, monitoring, and improving compliance with internal and external requirements. Participates in processes to prepare for, participate in, and follow up on Regulatory Agencies and certifications. Participates in processes to support compliance with PI standards, contributes toward continuous survey readiness activities and participates in the survey processes and findings.
7. Quality Review and Accountability – Facilitate and support compliance with voluntary, mandatory, and contractual reporting requirement for data acquisition, analysis, reporting and process improvement. May support practitioner and nursing performance review activities as directed.
8. Professional Engagement - Engages in the healthcare quality profession with a commitment to practicing ethically, enhancing one's competencies and advancing the field by integrating ethical standards into practice, engaging in lifelong learning and participating in activities that advance the profession, such as participation in professional organizations and achievement of certification in healthcare quality.
9. Responsibilities cross all levels of internal customers including the department, facility and system, and external customers including but not limited to the medical staff, the community, regulatory bodies and state agencies.
MINIMUM QUALIFICATIONS
Requires a Bachelor’s degree in nursing or other healthcare field (i.e.: Pharmacy, Physical Therapy, Respiratory Therapy, etc.).
If in a profession that requires licensure, current licensure/certification/registration is required for state worked.
Requires a proficiency level typically attained with five years acute care clinical experience.
Requires ability to perform complex statistical analysis and highly developed problem-solving skills. Requires the ability to manage programs and projects. Requires demonstrated excellence in interpersonal and written communication skills.
PREFERRED QUALIFICATIONS
Registered Nurse (RN) license preferred. Certified Professional in Healthcare Quality (CPHQ) certification is preferred.
Master’s Degree is preferred. Experience with process improvement, regulatory/accreditation programs, data management, and analysis including graphic development and presentations is highly desirable.
Additional related education and/or experience preferred.
EOE/Female/Minority/Disability/Veterans
Our organization supports a drug-free work environment.
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Rentokil Initial
Rentokil Initial is an international business services company employing 57,700 colleagues across 90 countries.
We strive to protect people and enhance lives, for example by controlling pests, and improving hygiene. We are experts in the fields we operate in, investing in training, science, innovation and technology. Listening and acting on feedback is part of our culture to support colleagues and our customers. Rentokil Initial regards equality and fairness as a fundamental right of all of its colleagues. We live our values of Service, Relationships and Teamwork which were identified by our colleagues across the world.
Awards
Rentokil InitiaI Philippines is officially ranked in the top three most engaged places to work in the Philippines, as part of the annual Korn Ferry Employee Engagement Awards 2018.
Philippine Best Employer Brand Awards 2019.
Find out more on careers.rentokil-initial.com
Your day-to-day responsibilities will include:
Do you have what it takes? If you want to be considered for this role you will need:
Are you interested? Here's what you can expect when you join us.
Benefits From Start Date
Benefits after 6 months of continuous work and pass the performance evaluation;
Rentokil Initial believes in supporting all employees to provide equal opportunities and avoid discrimination. We also place emphasis on workplace diversity which means that we are serious about creating an inclusive environment that accepts each individual's differences, embraces their strengths and provides opportunities for all colleagues to achieve their full potential.
Do you love to provide a valued professional service throughout your community? Do you feel like you could do the job well? Apply for the role today!
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Digital Asset Custody, globally, without compromise.
Zodia Custody is a FCA, CBI and CSSF registered Virtual Asset Service Provider (VASP), offering Digital Asset Custody services to Institutional Investors. Zodia Custody is a Venture backed by Standard Chartered Bank, Northern Trust and SBI Digital Asset Holdings based in the UK, Europe, Hong Kong, Australia, Singapore and Japan.
We have ambitious plans to scale internationally, by way of internal and external growth. Zodia Custody has also partnered in Japan with SBI to launch the service in APAC and has plans to continue to expand in APAC and Middle-East. We aim to be the best in class in providing Crypto Custodian services.
Zodia Custody is an institution-first digital asset custodian that does not compromise on its control standards. We are regulation first in everything we do. Within the Risk & Compliance departments, we are at the forefront of innovation and alongside our colleagues are engaged in safely developing Business Services to support the fast-structuring crypto-industry.
The Risk and Compliance Teams are responsible for allowing the business to scale sustainably, whether it involves new markets, products, blockchains and more. Our Teams are involved in end to end processes to mitigate risks, including financial crime risks, and identification of areas of control weakness. We work directly with the business as key partners in driving control improvement.
The teams are also responsible for identifying any gaps or weaknesses in Zodia’s adherence to applicable laws, regulations, rules and standards of self-regulatory organisations. Risk & Compliance play a key role in in ensuring key business processes help to manage risks enabling our businesses to continuously improve its risk management processes.
You’ll have the opportunity to work with both the Risk and Compliance teams, which are core teams to Zodia Custody’s success. You will help Zodia Custody in its mission to enable Digital Assets, without compromise.
What you'll be helping us with:
You'll spend your time:
Above all, we are looking for people that are excited about helping Zodia Custody scale in a compliant, thoughtful and controlled way.
Key Stakeholders
You should apply if:
We offer a range of fantastic benefits including:
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Control Risks' Embedded Consulting Practice is growing in Sydney, Australia, and we have a great opportunity for someone with a few good years of business continuity experience to join us.
Working as part of a dedicated team, this role will be embedded within a leading tech sector client and will provide holistic Business Continuity services including proactive consultation, guidance, and direct support to corporate and other stakeholders as required.
Responsibilities will involve:
Preferred:
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Aegros is Latin for ‘Patient’. We chose this name because it speaks to our focus on the patient. Every day we strive to place the patient first by providing therapeutic plasma products they would not otherwise be able to access.
At Aegros we believe access to life saving therapeutic plasma drugs is a human right and not a privilege. In a nutshell our mission is to put the patients first through innovation.
Over 30 years we have developed our HaemaFrac™ process which enables countries to turn human plasma they collected into life saving hyperimmune products.
It's no secret that Aegros is expanding rapidly! An exciting opportunity has arisen for a Senior Manufacturing QA Associate to join our Quality Assurance team. Reporting to Quality Assurance Manager, you will provide support in developing the company’s quality management system and assist peers with the daily running of the Quality Assurance Department.
What you will be involved in………
• Audit of production and QC documentation.
• Perform line clearance, pre and post production run.
• Support the QA Manager in the set-up and maintenance of QMS.
• Ensure QMS and operational compliance with regulatory requirements.
• Support for key QMS systems such as audits, CAPA, SOP review, etc.
• Support RA activities.
• Support in developing and implementing quality strategies.
• Deviation, NCR and complaint management, Products and Materials Release, Validation and Change Control Support, New production introduction and Documentation Controls to ensure an efficient operational Quality System that assures full compliance with company policies, regulatory requirements and cGMP.
• Responsible for ensuring that material supplied is fit for purpose for customer.
• Responsible for providing quality oversight for Operations activities.
• Support the QA Manager in continuous improvement projects and quality related improvement initiatives.
• Assist in internal audits and the review of validation reports.
• Issue and review batch documentation and release of batches of Intermediate, Bulk and Finished products.
What we would expect from you:
• Life Sciences (Chemistry, Microbiology, etc.) academic degree with experience in Pharmaceutical / Biopharmaceutical industry within Australia and Internationally.
• Experience in research and large-scale bioprocessing techniques.
• An understanding and experience of quality systems and the need to develop and follow SOPs, particularly in a cGMP environment.
• Strong interpersonal and communication skills.
• Ability to grasp new concepts quickly and to assimilate data from a range of scientific ideas.
• Ability to work under pressure and to strict guidelines.
• Ability to manage time and to delegate as appropriate.
Here’s what we can offer you…
• An environment which allows the individual to grow alongside the company
• A role that provides the bandwidth to explore innovative solutions while keeping patients at the centre of everything we do
• The chance to work with global industry experts in an organisation where success will be defined not just on successful delivery of goals but on how they were achieved
• A multicultural environment where every voice is heard
• Competitive remuneration package which includes an annual Bonus + Employee Share Options
• Close to public transport.
Interested? Apply today...!!!!
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Do you inspire people to learn? Are you a qualified, experienced trainer passionate about delivering best in class customer experiences who can deliver results?
We are looking for an experienced trainer to design, develop and roll out customer service excellence training to our national frontline teams.
Rentokil Initial is one of the largest business services companies in the world. Our company operates in all major economies of Europe, North America, Africa, Asia and the Pacific. The company has some 78,000 employees providing a range of support services in over 50 countries worldwide.
To be successful in this role you will display demonstrated understanding of Contact Centre CX concepts and a variety of interactions practices, quality initiatives, coaching and mentoring, internal sales and the unique demands of frontline staff.
In this role, you will:
Essential criteria:
Desirable criteria:
This is an exciting and challenging position with an organisation that values its people. In return you will be rewarded with a generous remuneration, onsite parking and ongoing support and training.
If this sounds like you, apply now!
Employee Testimonials -
“I love working at Rentokil - I love how the internal team bands together and getting to work with different customers every day.”
Matt Jones
"There's a sense of purpose in what I do. I get up and go to work to make sure that my people are safe, they're happy and our clients are serviced."
Darran Gibson
"I have been with Rentokil Initial for 15 years and they have always been there and supportive of me...so I have tried to carry that on as a manager myself."
Deb Morris
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The roles and responsibilities of a quality assurance varies across different industries. The duties include regulate, arrange and concur on quality procedures, standards and specifications, assess requirements and ensure everything is complied.
The type of jobs related to quality assurance encompass analyst, associate, maintenance technician, audio & video equipment technician, manager of quality assurance, quality assurance assistant manager, quality engineer, quality assurance technician, maintenance manager, safety technician, HVAC technician, consultant, coordinator, director, quality inspector, field service engineer, specialist and supervisor.
The role of quality control is to examine products and materials for defects or deviations from specifications. Responsibilities include monitor operations to ensure that they meet production standards, recommend adjustments to the assembly process, test products being produced, discuss inspection results and report inspection.
The role of quality assurance is to ensure a product or service meets the established standards of quality including reliability, usability and performance required for distribution. Responsibilities include devise sampling procedures, review the implementation of inspection system, document internal audits, investigate customer complaints, compile statistical quality data and analyse data to identify areas of improvement in the quality system.
The role of quality assurance/quality control(QAQC) engineer is to work with quality assurance supervisors, analysing manufacturing processes for improvement using various methods of testing and inspection. Responsibilities include implementing methods for process control, promote quality standards, assist in process certification and review suppliers purchase orders while establishing supplier quality requirements.
The role of QC inspector is to monitor the quality of incoming and outgoing products for a company. Responsibilities include reading blueprints to understand the requirements of products/services, measure product dimensions, recommend improvements to the production process to ensure quality control, document inspection outcomes by completing detailed reports, advise production team about quality control concerns to improve product excellence and supervise the production process.
