- Sokol Materials & Services (Skillman, NJ)
- …+ Knowledge of biotech, bulk drug substance or finished product manufacturing , medical device analytical testing ishighly desirable. + Extensive knowledge of ... Proven attention to details + Comfortable working in an FDA regulated environment. About the Role DUTIES AND RESPONSIBILITIES:...Provide QA support to the Devens site and QA Manager by reviewing and approving investigations and corrective actions… more
- Endo International (Rochester, MI)
- …in a body of information required for the job_ _e.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing , Six-Sigma, etc._ + Strong knowledge of ... 72 hours. May attend meetings in place of the Manager Quality Systems and determines priorities and make appropriate...+ Attends meetings as requested in place of the Manager Quality Systems and determines priorities and makes appropriate… more
- CVS Health (Mount Prospect, IL)
- …based control systems. + Performing preventative maintenance on equipment, notifying the Manager of any concerns regarding major repairs needed or any additional ... prioritize. + 3+ years of performing Preventive Maintenance (PM) to automated manufacturing equipment and utilizing LOTO procedures. + 3+ years of troubleshooting,… more
- AbbVie (Irvine, CA)
- …reviews. + Refine and develop selected concept(s) with little guidance from manager . + Investigate and evaluate materials, adhesives, and assembly techniques based ... members, + Help develop assembly procedures and assist in transfer methods to manufacturing . + Document ECO changes within the Document Control system. + Coordinate… more
- AbbVie (Pleasanton, CA)
- …reviews. + Refine and develop selected concept(s) with little guidance from manager . + Investigate and evaluate materials, adhesives, and assembly techniques based ... members, + Help develop assembly procedures and assist in transfer methods to manufacturing . + Document ECO changes within the Document Control system. + Coordinate… more
- Medtronic (Fridley, MN)
- …and compliance, we empower teams focused on research, innovation, development, and manufacturing . As a Calibration / Metrology Technician III, you will perform job ... intervals, and out-of-tolerance reporting. + Familiar with these regulations: FDA 21 CFR Part 820 cGMP, ISO 13485, ISO...computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions… more
- Actalent (St. Louis, MO)
- …for tracking finished production. + Place non-conforming products on hold for QC Manager 's review. + Pull and retain product samples. + Comply with all company ... as assigned. Essential Skills + Experience with GMP, quality inspection, GMP/ FDA regulations. + Proficient in Quality, Laboratory, Quality Assurance, QC, Document… more
- Actalent (Sanford, NC)
- …+ Ensure alignment with company quality systems and regulatory expectations ( FDA , EMA, etc.). + Participate in deviation investigations and CAPA implementation ... Work Environment The role is based in a pharmaceutical manufacturing facility with office space within the engineering compliance...may be some flexibility in working hours at the manager 's discretion. Pay and Benefits The pay range for… more
- Mentor Technical Group (Juncos, PR)
- …provides a comprehensive portfolio of technical support and solutions for the FDA -regulated industry. As a world leader in life science engineering and technical ... MPs. + Approve process validation protocols and reports for manufacturing processes. + Request Quality on incident triage team....Own site quality program procedures. + Designee for QA manager on local CCRB. + Review Risk Assessments. +… more
- Medtronic (Juncos, PR)
- …Have:** + Advanced Knowledge of EO and Ebeam sterilization + Familiarity with FDA , ISO 11135, ISO 11737, and other relevant standards for sterilization and ... + Ability to clearly communicate findings and collaborate with regulatory bodies, manufacturing teams, and R&D. + Fully bilingual. **Physical Job Requirements** The… more