to our growth, we’re looking to add a Quality Engineer located in Libertyville, IL. Reporting to the Sr Director, Quality, the... Quality Engineer will be to maintaining quality engineering programs, standards and improvements within the organization...
to our growth, we’re looking to add a Quality Engineer located in Buffalo Grove, IL. Reporting to the Quality Manager, the Quality... Engineer will be to maintaining quality engineering programs, standards and improvements within the organization...
Job Title Supplier Quality Engineer Job Description The Supplier Quality Engineer is a key member of Philips’ Sleep... quality and innovation. Conducts & reviews Design for Manufacturing and Assembly Technique (DFMAT), Supplier Approval Form...
Instruments. This role focuses on risk management, design verification, and quality engineering for NPD projects. The engineer...JOB TITLE: Sr. Quality Engineer JOB ID: 22117 LOCATION: Lafayette, CO 80026 (Onsite) DURATION: 12 Months PAY RATE...
verification & Risk Management (ISO 14971) , Failure Assessment (FMEA) - MUST HAVE Medical Device experience. Quality Engineer...Job Description: Quality Engineer w/ Design Quality Engineering experience, product quality support, design...
is preferred. 3-5 years of engineering experience related to Quality, preferably in an FDA regulated environment/Medical Device...Responsibilities: Senior Quality Engineer is responsible for leading and executing complex validations, driving...
, Design Control, Supplier Quality, medical device. Someone already experienced with Pharmaceutical would be preferred...Job Description: The Senior Engineer, External Manufacturing and Supplier Quality provides strategic and tactical...
, Design Control, Supplier Quality, medical device. Someone already experienced with Pharmaceutical would be preferred...Job Description: The Senior Engineer, External Manufacturing and Supplier Quality provides strategic and tactical...
Responsibilities: The Supplier Quality Engineer is responsible for managing finished goods Contract Manufactured (CM... part 820 regulations. Requirements: BS Engineering. 3+ years of Medical Device experience. PPAP experience...
. Minimum of 4+ years of work in medical device industry experience in Engineering, Quality and Supplier Quality... OR Advanced degree in Engineering field with 2+ years of work in medical device industry experience in Engineering, Quality...
' experience working in manufacturing of finished medical device or related industry. Working knowledge of the FDA Quality System...Job Description: As a Senior Supplier Quality Engineer, you have a unique impact on the quality and reliability...
Job Description: The Quality Engineer is responsible for providing quality assurance support for some or all the... of quality regulations: drug, biologics, device and/or combination products. Assist project teams in planning, preparation...
with minimal supervision and bring deep knowledge of medical device regulations, GMP, and supplier quality systems.... Take on additional duties as assigned with flexibility and adaptability. External Manufacturing & Supplier Quality. Medical Device...
experience related to Quality, preferably in an FDA regulated environment/Medical Device industry. Proven experience in the...Responsibilities: The Senior Quality Engineer is responsible for leading and executing complex validations, driving...
pharmaceutical, biologics, medical device, and combination product manufacturing operations. The Quality Engineer...Responsibilities: We are seeking an experienced Quality Engineer to join our team in Worcester, MA, supporting...
System, ISO, and medical device requirements Qualifications: Quality Engineer Qualifications Bachelor’s Degree...Overview: About rms Company rms Company provides contract manufacturing of high-quality, tight-tolerance medical...
Job Description: As a Quality Engineer for New Product Introduction (NPI) at Stryker, you will provide technical...). Maintain and review design history files (DHF) and risk management documentation per ISO 14971. Serve as a Quality lead...
's products. This role requires expertise in supplier, design, manufacturing, and software quality engineering. The engineer..., and production process control methodologies in a medical device environment. Previous work experience with product design changes...
Responsibilities: The Supplier Quality Engineer is responsible for managing finished goods Contract Manufactured (CM... part 820 regulations. Requirements: BS Engineering. 3+ years of Medical Device experience. PPAP experience...
industry, particularly within the medical device, bio-pharmaceutical, or biotechnology sectors, with a strong preference... 60601 and IEC 62304 experience is a plus. Experience in the medical device and/or regulated industry...