- Bristol Myers Squibb (Madison, NJ)
- …Promotion (OPDP) advisory submissions and subpart E and H submissions + Ensure full regulatory compliance of all promotions with approved labeling and /or FDA ... and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director Commercial Regulatory Affairs** **Description** :...guidances + Ensure regulatory compliance with subpart E/H and 2253… more
- Merck (Rahway, NJ)
- …Proper Documentation, Quality Control Management, Quality Management, Quantitative Assay, Regulatory Awareness, Regulatory Compliance , Regulatory ... **Job Description** The Associate Director, Quality Control within our Research and...within our Research and Development Division Device Quality & Regulatory is responsible for providing QA/QC oversight of the… more
- Capital One (New York, NY)
- …marketing and customer experience + Support to ensure adherence to legal and regulatory compliance requirements related to card issuance + Gather and report ... Principal Associate , Partnership Marketing ( Remote ) Capital One...store leadership and key internal partners (Marketing, Customer Experience, Compliance , etc.) to ensure a consistent and effective experience… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …a risk-based approach. **Key Responsibilities** * Monitor and assess global regulatory inspection outcomes, enforcement actions, quality and compliance metrics, ... advance benchmark inspection readiness and support a culture of quality and compliance . * Perform comprehensive on-site or remote inspection readiness… more
- Bristol Myers Squibb (Madison, NJ)
- …of the commercial program (vector, gene editing and cell therapy projects) to ensure regulatory compliance of GMP operations in support of the program.The PQL ... programs that are appropriate for a commercial program along with associated regulatory expectations and global compliance requirements. T he individual will… more
- Merck (Rahway, NJ)
- …Name Development, Process Improvements, Professional Presentation, Project Management, Regulatory Compliance , Strategic Planning **Preferred Skills:** Current ... the brand while ensuring adherence to internal processes and regulatory guidelines. To prepare for these launches, we are...prepare for these launches, we are looking for an ** Associate Director (AD)** to join our center of excellence.… more
- Merck (Rahway, NJ)
- …launch in alignment with the company's business goals, and quality and regulatory compliance . **Essential Duties and Responsibilities:** + Program Leadership and ... **Job Description** The Associate Director- Device Tech Transfer is a leadership...Build strategic partnerships with manufacturing sites and partner groups ** Regulatory Compliance and Quality Assurance:** + Ensure… more
- Ankura (New York, NY)
- … examinations. Once a company is licensed, Ankura can serve as the overall state regulatory manager in the US to ensure compliance with a myriad of state ... rules and regulations. Our compliance professionals can support all regulatory reporting...and licensing requirements and will keep clients abreast of regulatory changes. We are seeking a Senior Associate… more
- Bristol Myers Squibb (Princeton, NJ)
- …** + Ensure that business rules and model-driven recommendations operate within compliance , legal, and regulatory guardrails for pharmaceutical promotion. + ... cross-functional collaboration and communication skills. + Familiarity with governance, compliance , and regulatory requirements in US pharmaceutical… more
- Bristol Myers Squibb (Princeton, NJ)
- …This role provides medical oversight, ensures scientific rigor, and supports regulatory and compliance needs, collaborating closely with cross-functional ... Read more: careers.bms.com/working-with-us . **Position Summary:** The Established Brands Associate Director, Medical Affairs, is responsible for leading and… more
- Bristol Myers Squibb (Princeton, NJ)
- …with Program Managers, vendors, and cross-functional teams to ensure operational excellence, compliance , and improve patient access. The Associate Director will ... address maximizer/accumulator/AFP/cash-pay discount cards negatively impacting GTN + Ensure compliance with regulatory and company policies related to… more
- Merck (Rahway, NJ)
- **Job Description** We are currently seeking an Associate Principal Scientist (Engineer) for our Pharmaceutical Commercialization Technology (PCT) team. PCT is ... development of primarily oral solid dosage forms from Phase IIb through regulatory filings, process performance qualification, and into commercial supply. Our work… more
- Bristol Myers Squibb (Madison, NJ)
- …and regulatory requirements. . + Monitor and evaluate the evolving regulatory landscape to ensure compliance and best practices in benefit-risk assessment. ... across the organization, including medical safety assessment, clinical development, global regulatory , epidemiology and others. The SBRA Lead will drive functional… more
- Merck (Rahway, NJ)
- …As we prepare to bring this asset online, we are seeking an Associate Director, Operations to lead the end-to-end operational strategy, execution, and performance of ... that meet cGMP, aseptic processing, and safety requirements. In parallel, the Associate Director, Operations will design and execute a comprehensive hiring and… more
- Merck (Rahway, NJ)
- **Job Description** ** Associate Principal Scientist - Device Technical and Engineering Lead ( Associate Director Equivalent)** _Our company's Device Product & ... ensure products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements. This position will lead… more
- Merck (Rahway, NJ)
- **Job Description** ** Associate Principal Scientist, Analytical Commercialization Technology** The Analytical Commercialization Technology (ACT) group within ... Analytical Chemistry in Development and Supply (ACDS) is seeking applicants for an Associate Principal Scientist position available at the Rahway, NJ and West Point,… more
- Bristol Myers Squibb (Princeton, NJ)
- …The role partners closely with Translational Medicine, Clinical Development, Regulatory /QA, Finance/Legal, and external CRO/IVD partners to shorten cycle times, ... control rigor (risk management, traceability, DMR/DHR readiness) and partner with Regulatory /QA on submissions and audits. + Integrate diagnostic strategies into… more
- Bristol Myers Squibb (Princeton, NJ)
- …updates ** Compliance & Quality Focus** + Ensures tagging meets regulatory and quality standards required for the Pharmaceuticals industry + Proactive approach ... in their personal lives. Read more: careers.bms.com/working-with-us . **Summary:** The Associate Director, Tagging & Taxonomy Enablement is accountable for applying… more
- Bristol Myers Squibb (Summit, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . The Associate , Equipment Commissioning & Qualification (ECQ) Delivery supports the successful ... Commissioning and Qualification Activities: + Maintain qualified equipment systems in compliance with policies, guidelines and procedures. + Assist in the… more
- Bristol Myers Squibb (Princeton, NJ)
- …more: careers.bms.com/working-with-us . **Position Summary:** We are seeking an experienced Associate Director, Customer Experience (Cx), Patient & Care Partner to ... access measures, digital engagement). + Monitor industry trends, competitor offerings, and regulatory changes in the behavioral health market. + Build and nurture… more