- Burns & McDonnell (Morristown, NJ)
- **Description** The Senior Architect - Process will lead in the development of pharmaceutical and life science projects teams to create world-class designs for Life ... effective management of change orders. + Applies knowledge and understanding of FDA , cGMP, and other concepts, practices, codes, and procedures within the industry.… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …transparency. This is a quality assurance role, helping maintain global compliance , reinforcing audit excellence, and ensuring the consistent delivery of ... oversight and completion of assigned tasks. + Track resources and ensure compliance with regulatory timelines and quality standards for audit deliverables. + Support… more
- J&J Family of Companies (Raritan, NJ)
- …clinical supplier quality point of contact to ensure quality of the GxP system, compliance with regulatory requirements and SOPs, and to ensure a continued state of ... mitigations, conduct qualification audits and provide guidance to ensure compliance with Good Clinical Practices (GCP), external regulations/ requirements, and… more
- Terumo Medical Corporation (Somerset, NJ)
- …Blood and Cell Technologies, Inc. (collectively "Terumo"), including ensuring compliance with privacy laws and regulations, developing and implementing privacy ... and regulations. Will be responsible for protecting Terumo against legal and compliance risks related to privacy and data management. Additionally, the Senior… more
- Merck (Trenton, NJ)
- …management, communication, and networking skills + A thorough comprehension of FDA , OIG, HIPAA, and other ethical guidelines, laws, and regulations relevant ... to the pharmaceutical industry and its customers + Ability to organize,...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance **Los… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- **Job Description Summary** As Associate Director of Technical Solutions at BD Pharmaceutical Systems, this role holds a strategic position in managing the customer ... experience management for high-stakes clients as Associate Director at BD Pharmaceutical Systems. **Key Responsibilities include:** + Lead the strategy for managing… more
- Sokol Materials & Services (Skillman, NJ)
- …Minimum of 3 years of experience in CQV and/or CSV within the pharmaceutical , biotechnology, cell therapy or medical device industries. + Experience with Cell ... including risk-based validation approaches. + Knowledge of regulatory requirements, including FDA , EMA, and ICH guidelines. Knowledge, Skills & Abilities: +… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …This role is responsible for ensuring the robustness, scalability, and compliance of downstream operations through effective technology transfer, validation support, ... operations. + Experience with cGMP manufacturing environments and regulatory requirements ( FDA , EMA, ICH). + Familiarity with process validation principles and CPV.… more
- Robert Half Legal (Mahwah, NJ)
- Description Our client, a research-led, innovative, global pharmaceutical company, is looking for a senior corporate paralegal to join their team in Elmwood Park, ... expert for current e-billing system. * Proactively manage all invoices for compliance with outside counsel guidelines and approve invoices pertaining to legal… more
- BrightSpring Health Services (Totowa, NJ)
- …room areas and related equipment are cleaned, sanitized and maintained in compliance with company policies and procedures. + Obtain supply inventories form ... meetings and quality improvement activities. + Adhere to all accreditation, OSHA, FDA , state, local and federal regulations and standards relevant to infusion… more