- Reckitt (Parsippany, NJ)
- …in development and manufacturing in the consumer goods, pharmaceutical, or medical device industries. + Must have experience with quality tools such as: SPC, ... appropriate law. **Nearest Major Market:** New York City **Nearest Secondary Market:** Newark **Job Segment:** Medical Device , Counseling, Nutrition, Healthcare more
- embecta (Parsippany, NJ)
- …is a critical role within embecta, a global leader in medical device manufacturing. This position ensures that all quality systems and operations comply ... regulatory requirements, including FDA and ISO standards. The Quality Compliance Auditor plays a strategic role in maintaining...quality compliance or a related role within the Medical Device or Pharmaceutical manufacturing industry. +… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …degree and 15+ years of experience in a FDA regulated pharmaceutical and/or medical device industry environment + Strong knowledge of current global Good ... an experienced and dynamic Executive Director of R&D Global Quality to join our team. This pivotal role will...Previous experience of working in the global pharmaceutical and medical device industry. + Experience working with… more
- Sanofi Group (Morristown, NJ)
- …science, or equivalent with at least 10 years relevant experience in the pharmaceutical, biotech, medical device or a related industry or at a Regulatory ... **Job Title:** Global Quality Lead, GMP, GDP Audit and Inspection -...secure product launches and support compliance through audits, inspections, regulatory surveillance, and advocacy. Grounded in core values Integrity,… more
- Merck (Rahway, NJ)
- …advanced degree (Master's or PhD) preferred. + Minimum of 10 years of experience in medical device or combination product engineering, with at least 5 years in a ... + Demonstrated technical leadership in Technology Transfer and Design Transfer for medical device and combination product component manufacturing, assembly, and… more
- Merck (Rahway, NJ)
- …and Skills: . **Manufacturing** - Injection Molding and Automated Assembly of Medical Device Components. Final Assembly and Packaging of Combination Products. ... Vaccine Products. Our team works with a "Safety First, Quality Always" mindset. As the primary point of contact...development and manufacturing for MDCP (21 CFR Part 4, Medical Device Reporting, ISO 13485:2016, EU … more
- Integra LifeSciences (Plainsboro, NJ)
- …corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to ... patient outcomes and set new standards of care. The ** Quality Inspector I** will be responsible for performing ...clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. + QA experience in… more
- Integra LifeSciences (Plainsboro, NJ)
- …corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to ... patient outcomes and set new standards of care. The ** Quality Inspector I** will be responsible for performing ...clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. + QA experience in… more
- Integra LifeSciences (Plainsboro, NJ)
- …corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to ... patient outcomes and set new standards of care. The ** Quality Inspector I** will be responsible for performing ...clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. * QA experience in… more
- Merck (Rahway, NJ)
- …**Required Experience and Skills:** + Experience in the pharmaceutical, biotechnology, chemical, medical device , or closely related industry. + Experience in one ... GMP documents. + Ensure all API are manufactured in compliance with cGMP and regulatory filings. + Perform independent quality review and approval of batch… more