| Job alert | Jobs 1 - 10 of 366 |
PRIVATE LABEL COMPLIANCE SPECIALIST I
NOW Foods
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Bloomingdale, IL, 60108
... This responsibility includes but not limited to knowledge of FDA-CFR reference, regulatory compliance of certi Permanent - May 03
Sr. Electrical / Firmware Engineer
Ontogen Medtech
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Lisle, IL, 60532
... creative electrical design solutions to abstract problems Demonstrated experience generating product ideas and developing through to production Experience with medical device development and FDA quality practices and standards, including ISO 13485; ... - Apr 21
Specialist, Quality Assurance -Change Control
Sagent Pharmaceuticals
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Schaumburg, IL, 60195
... Work in partnership with Regulatory Affairs, Global Alliance Management, Labeling and CMOs to ensure Sagent’s requirements for changes are met in accordance with FDA requirements. Support the existing Quality Management System (QMS) including ... - Apr 11
Director of Manufacturing
Newmedical Technology, Inc.
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Northbrook, IL, 60065
... Regulatory Compliance: Ensure compliance with regulatory standards and requirements relevant to medical devices or OTC products, such as FDA regulations, ISO standards, and Good Manufacturing Practices (GMP). Implement and maintain processes to ... - Apr 17
Quality Lab Manager - Medical Devices
Medical Murray
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Barrington, IL, 60010
... Minimum Qualifications: BS or MS in technical, life sciences, or engineering discipline Knowledge and understanding of ISO 13485, ISO 17025, and FDA 21 CFR Part 820 cGMP standards Quality assessment/audit experience is desirable 3-5 years in Quality ... - Apr 27
Delivery Technician - No Experience
Prism Health Care Services
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Schaumburg, IL, 60196
... * Ensure compliance with OSHA FDA, DOT and ACHC requirements; maintain necessary logs. * Assist with equipment cleaning and maintenance when required. * Assist warehouse staff with inventory control. * Place any dirty or contaminated equipment in ... - Apr 29
Quality Assurance Manager
CMIC, Inc.
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Hoffman Estates, IL
... · Solid understanding of FDA regulations relating to GLP, 21 CFR Part 58 and Part 11. · Sound understanding of quality systems pertaining to contract research supporting Pharmaceutical industry and good documentation practices within a CRO, life ... - Apr 11
Sanitation Manager
Sterling Engineering
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Bartlett, IL, 60103
... Understanding of GMP, SQF audits, FDA, PMO, HACCP, and OSHA requirements. Strong leadership and team management skills. Excellent communication and interpersonal skills. Detail-oriented with a commitment to cleanliness and hygiene standards. Fluency ... - May 04
Regulatory Affairs Specialist
Medline Industries LP
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Northfield, IL
... Applied knowledge of FDA regulations and guidelines. Ability to evaluate information to determine compliance with standards, laws, and regulations. Travel required up to 5%. 795813 - May 02
Validation Engineer
Automated Systems, Inc.
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Round Lake, IL
... In this role, the Validation Engineer will lead specific C&Q activities for pharmaceutical manufacturing equipment and processes, ensure compliance with quality standards/requirements, and industry standards (FDA, EMA, ISO, ICH, etc.). In this ... - May 04