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Leidos has an opening for a Fire Protection Engineer at NASA Glenn Research Center in Cleveland, Ohio. The primary functions for the Fire Protection Engineer are to provide support to the Facilities Infrastructure Division for Fire Protection and Life Safety. Services provided will ensure that Building and Fire Codes, NFPA, Life Safety Codes and NASA standards are identified and addressed in the concept and requirement phases, incorporated into the facility design and acquisition phases, and implemented in the facility construction.
Primary Responsibilities:
Basic Qualifications:
Preferred Qualifications:
Must be able to pass a Public Trust background investigation.
While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above.
The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.
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Looking for an opportunity to make an impact?
The National Security Sector at Leidos combines technology-enabled services and mission software capabilities in the areas of cyber, logistics, security operations, and decision analytics to support our defense and intel customers’ mission to defend against evolving threats around the world. Our team’s focus is to ensure our customers have the right tools, technologies, and tactics to keep pace with an ever-evolving security landscape and succeed in their pursuit to protect people and critical assets.
Your greatest work is ahead!
The CSS Operation at Leidos is seeking a motivated individual to work in a dynamic environment with a team of Cyber Engineers in reverse engineering, vulnerability research, prototyping, design, development, integration, and test tasks to develop capabilities against various networking devices. This work will leverage your ability to deconstruct and tear-down of a variety of hardware and software, focusing on network devices and technologies, and developing capabilities to utilize the vulnerabilities discovered. The candidate must be experienced in working with a dynamic team of cyber researchers and engineers through all stages of the product lifecycle – from vulnerability research to development and test. This position is contingent upon contract award.
What you’ll be doing:
What does Leidos need from me?
Favorable if you have:
While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above.
The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.
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A qualified candidate will be self-motivated with strong technical and analytical skills as well as possess practical and hands-on approach to engineering control in the areas of metrology management
Responsibilities:
· Recipe creation and optimisation for new R&D applications requirement.
- Preventive and corrective maintenance planning cum execution and vendor management.
· To take charge of new tools technical assessment and tender creation (equipment cum process application startup) and service contract tender set-up
· Drive continuous improvement projects (CIP) to achieve better measurement repeatability (MSA, GR&R, SPC etc).
· To set-up appropriate process and product control plan and out of control action plans (OCAP)
· Provide technical training to related staff on best-known practices in terms of application metrology recipe creation.
Requirement:
· Diploma/Bachelor degree in Electrical and Electronics, Material, Physics or Chemical engineering
· Minimum 3~5 years of hands-on semiconductor experience (preferably in metrology application and equipment maintenance)
· Possess computer soft ware skills (i.e. JMP, Minitab, SQL, Visual basic, etc)
· Knowledge in problem solving and quality control skills (i.e. LEAN 6sigma, RCA, DOE, etc)
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Responsibilities:
Qualifications:
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Job Summary:
We are seeking a skilled and experienced Mechanical Design Engineer to join our dynamic team. The successful candidate will be responsible for designing and developing mechanical systems and components for DxD Hub. The role involves collaborating with cross-functional teams, utilising CAD software, conducting feasibility studies, verification testing and ensuring designs meet technical and regulatory requirements.
Roles and Responsibilities
· Conceptualise, design, and develop mechanical components and mechanisms for medical devices
· Prepare and maintain design documentation such as specifications, bill of materials, test protocols, test reports, etc.
· Perform structural analysis, thermal analysis, and other relevant tests to validate and optimise designs.
· Conduct feasibility studies to assess the viability and performance of proposed designs.
· Work closely with cross-functional teams, including biological scientists, electrical engineers, software engineers, and project managers.
· Ensure compliance with DxD Hub Quality Management system, standards, and regulatory requirements such as FDA and ISO13485 etc.
Key Requirements
· Bachelor’s Degree in Mechanical Engineering, or related field. Master"s degree is a plus.
· Minimum 2 years of experience in mechanical design engineering.
· Proficient in CAD software, such as SolidWorks or AutoCAD.
· Strong understanding of engineering principles, materials, and manufacturing processes.
· Excellent problem-solving and analytical skills.
· Effective communication skills and ability to work collaboratively in a team.
· Knowledge in quality, product verification test, QMS, and ISO13485 would be an advantage.
· Self-driven team player who is able to work in a fast-paced environment.
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A qualified candidate will be self-motivated with strong technical and analytical skills as well as possess practical and hands-on approach to engineering control in the areas of metrology management
Responsibilities:
· Recipe creation and optimisation for new R&D applications requirement.
- Preventive and corrective maintenance planning cum execution and vendor management.
· To take charge of new tools technical assessment and tender creation (equipment cum process application startup) and service contract tender set-up
· Drive continuous improvement projects (CIP) to achieve better measurement repeatability (MSA, GR&R, SPC etc).
· To set-up appropriate process and product control plan and out of control action plans (OCAP)
· Provide technical training to related staff on best-known practices in terms of application metrology recipe creation.
Requirement:
· Diploma/Bachelor degree in Electrical and Electronics, Material, Physics or Chemical engineering
· Minimum 3~5 years of hands-on semiconductor experience (preferably in metrology application and equipment maintenance)
· Possess computer soft ware skills (i.e. JMP, Minitab, SQL, Visual basic, etc)
· Knowledge in problem solving and quality control skills (i.e. LEAN 6sigma, RCA, DOE, etc)
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Responsibilities:
Qualifications:
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Role Summary/Purpose
Suntar is looking for a highly driven individual equipped with relevant technical skills in ensuring the smooth implementation of electrical design, PLC and HMI programming, installation, and commissioning of industrial membrane separation projects. Participate in project bidding, electrical after-sales service, etcs.
Responsibilities
· Electrical design of engineering projects, control programs for engineering projects, installation, commissioning, execution and supervision of engineering projects.
· Liaise with related parties and ensure smooth operation
· Compilation and summary of project completion materials.
· Participation in preliminary project design and technical support.
· Learning and application of new technologies and processes, design and development of control for new processes and products, assisting in the formulation and improvement of company's electrical control standardization documents.
· Ensure assigned tasks are completed on time
Qualifications / Requirements
· Bachelor's degree or higher in Electrical Engineering, Electrical Automation, Mechatronics, or related fields
· Ability to independently manage the design, installation, and commissioning of large-scale projects
· Minimum of 2 years of experience in engineering installation, commissioning, and troubleshooting
· At least 3 years of related experience in water treatment industry
· Willingness and ability to travel as required
· Strong sense of responsibility, resilience, and teamwork spirit, with a dedication to professional ethics.
· Responsible, resourceful, independent and proactive individual yet able to work well in a team
· Fluency in other regional languages/dialects is a plus, because the role require the candidate to deal international client from other region (Chinese, Hokkien etc.)
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Join the Innovation at ISCE2: Seeking a Visionary and Talented Scientist
Are you ready to be a part of a dynamic, forward-thinking team to drive the future of green and sustainable technology in biomanufacturing?
ISCE2 is actively looking for a passionate Scientist with proven track record in chemical biology, biocatalysis or biotechnology research to join our multi-disciplinary team to develop next generation green and sustainable technology for the manufacturing of fine and specialty chemicals.
What Sets Us Apart:
Next-Generation Technology: Be at the forefront of innovation, utilizing advanced technologies, including automation, data science, AI and machine learning, to accelerate development.
Key responsibilities:
The successful candidate may be responsible for but not limited to:
Requirements:
What We Offer:
The above eligibility criteria are not exhaustive. A*STAR may include additional selection criteria based on its prevailing recruitment policies. These policies may be amended from time to time without notice. We regret that only shortlisted candidates will be notified.
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Join the Innovation at ISCE2: Seeking a Visionary and Talented Scientist
Are you ready to be a part of a dynamic, forward-thinking team to drive the future of green and sustainable technology in biomanufacturing?
ISCE2 is actively looking for a passionate Scientist with proven track record in chemical biology, biocatalysis or biotechnology research to join our multi-disciplinary team to develop next generation green and sustainable technology for the manufacturing of fine and specialty chemicals.
What Sets Us Apart:
Next-Generation Technology: Be at the forefront of innovation, utilizing advanced technologies, including automation, data science, AI and machine learning, to accelerate development.
Key responsibilities:
The successful candidate may be responsible for but not limited to:
Requirements:
What We Offer:
The above eligibility criteria are not exhaustive. A*STAR may include additional selection criteria based on its prevailing recruitment policies. These policies may be amended from time to time without notice. We regret that only shortlisted candidates will be notified.
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Job Requirements:
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A healthy heart is essential to good health. That's why we're committed to advancing treatments for people with cardiovascular disease. As a global leader in Cardiac Rhythm Technologies, our breakthrough medical technologies help restore people's health so they can get back to living their best lives, faster. We focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.
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:
Career development with an international company where you can grow the career you dream of .
Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
An excellent retirement savings plan with high employer contribution
Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
Our Minnetonka, MN location currently has an opportunity for a Engineer I, Research and Development.
Engineer I, Research and Development, under general supervision, is responsible for providing engineering support to device manufacturing operations. Develops and implements efficient, cost-effective process improvements and work on delivery tools, such as catheters and introducers. Work requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more academic course of study and applying engineering and scientific principles to evaluating and solving technical problems. Stays abreast of and communicates technical advancements to colleagues and associates. Identifies and routinely uses the most effective, cost-efficient, and best practices to execute processes; continually evaluates their effectiveness and appropriateness.
WHAT YOU’LL DO
Provide engineering support for existing operations
May perform dimensioning and tolerance evaluations of components, drawings and tooling
May perform electrical analysis of failed components or devices for troubleshooting and corrective action purposes
Oversee device configuration control and modifies the configuration as required
Write Engineering Test Reports (ETR’s), memos, Engineering Change Papers, create travelers, and develop written operator procedures
Perform process validations on equipment and processes as required.
Resolve and/or facilitate the resolution of problems, including identifying causes to prevent re-occurrence
Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
Qualifications
Bachelors Degree in Mechanical Engineering, Biomedical Engineering or related field.
Minimum 1 year of relevant design and manufacturing work experience as related to medical devices.
Demonstrated ability to analyze and evaluate technologically complex devices.
Experience working in a broader enterprise/cross-division business unit model preferred.
Ability to work in a highly matrixed and geographically diverse business environment.
Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
Ability to leverage and/or engage others to accomplish projects. Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
Multitasks, prioritizes and meets deadlines in timely manner. Strong organizational and follow-up skills, as well as attention to detail.
Ability to travel approximately 5%, including internationally.
* 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
$48,000.00 – $96,000.00In 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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Wherever you work and whatever role you fill, when you represent the Bridgestone name you know that you are a valued teammate who is part of our larger mission to “Serve Society with Superior Quality.” We start by offering each teammate more than just a salary. We provide formal training, competitive performance incentives, paid vacation and holidays, healthcare packages for full-time and part-time employees, and a 401k plan to help build your future.
We believe people can only provide superior service and quality to others when they are allowed to bring their whole selves to work and know they are supported. We believe in championing all perspectives, individuals and teams because we understand the importance of seeing the world and our business through many different lenses. We are building a team as diverse as the world we serve. So, show us what you’re made of. Show us the smart stuff, the tough stuff, the bold, beautiful and brave stuff. Because who you are is what we need.
Bridgestone Americas, Inc. is headquartered in Nashville, Tennessee and is the U.S. subsidiary of Bridgestone Corporation headquartered in Japan. Bridgestone Americas and its subsidiaries develop, manufacture and market a wide range of Bridgestone, Firestone and associate brand products to address the needs of a broad range of customers and industries.
Responsibilities:
• Keeping Safety First and maintaining a safe work environment as "The Top Priority".
• Works on repair and maintenance problems of moderate scope and assists with projects or processes while receiving general instructions from higher level professionals
• Participates in planning and coordination of maintenance work, including review of mechanical specifications
• Performs reviews of proposed new equipment designs for reliability, ease of maintenance, and availability of replacement parts
• Liaises with production staff to coordinate repair work, statutory safety inspections and supply of new plant and equipment with production schedules
• Participates in the installation and commissioning of new equipment
• Supports continuous improvement/automation activities
• Other duties as assigned
Minimum Qualifications
6+ years of relevant work experience;
GED or equivalent
Preferred Qualifications
Associates' Degree in Applied Sciences
Typically requires an Associate's Degree and a minimum of 6 years of related experience; or equivalent work experience
Bridgestone is proud to be an Equal Employment Opportunity / Affirmative Action employer. It is our policy to consider for employment all individuals regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, gender, sex, sexual orientation, gender identity and/or expression, genetic information, veteran status, or any other characteristic protected by federal, state or local law.
Employment Eligibility
If hired, a Form I-9 Employment Eligibility Verification must be completed at the start of employment. Temporary work authorization or the need for sponsorship may disqualify you from employment.
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At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. Join our team to help people #SeeBrilliantly!
We foster an inclusive culture and are looking for diverse, talented people to join Alcon and we are looking for an Associate Director, Reprocessing Engineering to join our team in Lake Forest, CA.
Responsibilities:
As corporate SME interprets regulatory standards or guidance relating to reprocessing and translates into local and corporate procedures.
Establishes global implementation strategy and timelines for new or updated standards.
Provides detailed analysis of standards and impact on existing technical files. Partners with sustaining engineers to properly maintain reusable product technical files.
Proactively monitors literature, standards, industry guidance, trends, and customer reprocessing expectations globally.
Rapidly assimilates new technology and requirements, evaluates long term organizational needs in reprocessing.
Monitors and represents Alcon globally on select reprocessing standards committees.
Collaborates with Marketing, CASs, and HFE's to optimize reprocessing for customers and create global competitive advantage.
Guides NPI teams globally in developing suitable reprocessing methods, instructions, and requirements.
Guides engineers during product lifecycle activities relating to reprocessing requirements.
Provides guidance to reprocessing label development or updates to meet evolving regulatory and customer requirements.
Provide SME input during regulatory or corporate audits, and regulatory submissions.
Collaborates with RA/QA and Med Info Teams to develop materials to address customer inquiries.
Provides SME input for inquiries from customers, regulators, or Alcon staff relating to execution, content, and alternatives to reprocessing instructions.
Major Accountabilities
Performs corporate level assessments of emerging, newly published, or recently altered standards impacting the reprocessing field.
Leads critique/evaluation of product design and directions for use with respect to reprocessing objectives.
Provides expert technical guidance, maintains local and corporate reprocessing procedures, directs/conducts reprocessing verifications.
Works with teams to address reprocessing challenges, design reprocessing methods, and validate methods to support project objectives.
Develops superior cleaning, disinfection, drying, and sterilization test methods as needed to advance state of the art practices and customer needs.
Provides QA/RA with summaries or guidance in regulatory submissions, audits, or preparing IFUs.
Develops in-depth understanding of configuration, application, and engineering of reusable devices, establishes product families and adoption practices.
Leads efforts to select/approve external labs as strategic partners in developing better reprocessing regimens; develops in house test methods as feasible.
Collaborates with PSE to ensure technical files are updated as needed to stay compliant to current standards.
Lead efforts to address customer inquiries, develop FAQ resources with RA/QA or Global Med Info groups.
Create (or oversee) protocols, coordinate testing, verification reports, needed to support reprocessing instructions. Identify when reverification is required.
Experience:
10+ years of experience in QSR/EU MDR compliant medical device development including ability to:
Provide global technical leadership. Influences effectively in a cross-functional environment (e.g. multi-site, NPI, customer inquiry support)
Provide SME interpretation of: ISO 11135, ISO 11138-X, ISO 10993-X, ISO 17664-1/-2, ISO 17665-X, ISO 11607-X, ISO 15883-X, EN 13060, EN 285, AAMI ST 79, AAMI TIR 12/30, AAMI ST8, AAMI ST98, ISO 14161, EN 14885, EN ISO 11737-X, FDA Endotoxin and Reprocessing guidelines, RKI Guidance, MHP Central Sterilization supplements.
Effectively communicate complex concepts in presentations, regulatory submissions, and in technical reports to global audiences.
Develop reprocessing methods, lead IFU validations, resolve cleaning and sterilization concerns during development.
Apply detailed knowledge of common microbiological and biochemical laboratory methods (sterility & disinfection testing, protein/TOC/endotoxin assays, etc.)
Key Requirements/Minimum Qualifications:
Bachelor’s Degree or Equivalent years of directly related experience (or high school+15 yrs; Assoc.+11 yrs; M.S.+4 yrs; PhD+3 yrs)
The ability to fluently read, write, understand, and communicate in English.
7 Years of Relevant Experience
Work hours: M-F, standard
Travel Requirements: 10%
Relocation assistance: yes
Sponsorship available: yes
#LI-DNI
ATTENTION: Current Alcon Employee/Contingent Worker
If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.
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Total Rewards
Alcon’s Total Rewards programs are designed to align to incentives with business goals, encourage the right values and behaviors, and deliver long-term value. The first layer of our rewards program is compensation. We offer a combination of fixed pay and variable pay, which includes short-term incentives, and long-term incentives for eligible population. Our benefits program provides security for life events through life and disability insurance, supports savings for retirement, promotes good health and well-being and supports associates and their families during times of illness. To learn more about Alcon’s Corporate Social Responsibility including our Total Rewards, click here
Pay Range
$132,560.00 - $198,840.00
Pay Frequency
Annual
Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.
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At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers.
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Sr. Validation Engineer supporting Manufacturing Science & Technology, you will be trusted to work on design, develop, and implement new or revised production processes for the efficient/economical mass production of goods at Sinking Spring, PA.
ATTENTION: Current Alcon Employee/Contingent Worker
If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.
Find Jobs for Contingent Worker
Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.
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