- Bristol Myers Squibb (Princeton, NJ)
- …for regulated bioanalytical studies and CDx development, ensuring high quality, compliance , and timely delivery of internal and outsourced projects. This role ... liaison with CROs and external partners, managing study milestones, deliverables, and compliance with BMS quality systems and regulatory standards. ** Compliance … more
- Catalent Pharma Solutions (Princeton, NJ)
- …with Raw material work by being responsible for ensuring the quality and compliance of raw materials used in pharmaceutical manufacturing. This role involves ... testing, support method development/validation, and ensure audit readiness. + Maintain compliance with SOPs and regulatory requirements ( FDA , EMA, cGMP)… more
- BioLife Plasma Services (Trenton, NJ)
- …management. Gain exposure to real-world challenges such as audit processes, compliance requirements, and team performance management. + **Production Environment & ... service by assisting with production tasks while maintaining strict regulatory compliance and safety standards. + **Develop Leadership and Employee Relations… more
- Pfizer (Parsippany, NJ)
- …management or within a Health Authority. + Extensive knowledge of the pharmaceutical industry including Pharmacovigilance and ICH compliance regulations and ... equivalent) with commensurate experience in inspections, audits, quality and compliance . Experience: + 3-4 years minimum experience focusing on Pharmacovigilance,… more
- L'Oreal USA (Clark, NJ)
- …and finished products developed by, or acquired by L'Oreal USA, in compliance with global regulations and guidelines. This position requires an in-depth working ... of highly technical individuals responsible for the review and compliance of the safety of raw materials and finished...may have local and global regulatory impacts (CIR, RIFM, FDA , ANVISA, Health Canada, and other testing requirements of… more
- Actalent (Princeton, NJ)
- …testing, and routine lab operations to ensure product and facility compliance with GMP standards. Responsibilities + Perform environmental monitoring (EM) of ... in laboratory notebooks and electronic systems, ensuring data integrity and compliance . + Assist in investigations related to out-of-specification (OOS) results or… more
- Integra LifeSciences (Plainsboro, NJ)
- …set new standards of care. The **Quality Assurance Engineer II** will provide Quality compliance support on all aspects of the Plainsboro, NJ CMC Quality System. The ... that the development, manufacture and distribution of medical products is in compliance with corporate policies, US Food and Drug Administration regulations, ISO… more
- Fujifilm (Trenton, NJ)
- …diagnosed per year, number of hepatologists). + Adheres to company and compliance guidelines, policies, and procedures. + Effective communication within FUJIFILM IVD ... organization of sales, quality and compliance issues. + Utilization of the IVD reporting systems...with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard… more
- IQVIA (Parsippany, NJ)
- …destination platforms and provide offline & online matches. + Responsible for full compliance and adherence to FDA Pharma Guidelines (where applicable). + Work ... digital media planning (2 plus years) + Exposure to Medical / Pharmaceutical digital marketing industry + Expertise in overall programmatic landscape, programmatic… more
- Capgemini (Titusville, NJ)
- …for internal and external stakeholders + Ensure all documentation aligns with FDA , EMA, ICH, and other relevant regulatory standards + Support audits and ... bring:** + 3-5+ years of experience as a Technical Writer in the pharmaceutical or life sciences industry + Strong understanding of validation processes (equipment,… more