- Sanofi Group (Bridgewater, NJ)
- **Job Title:** Associate Director of Training-Patient Support Services **Location** : Cambridge, MA, Bridgewater, NJ **About the Job** The US Patient Support ... goals and to continuously develop a service excellence organization. The Sanofi Associate Director of Training- Patient Support Services (PSS), reports to… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Product Development Princeton, NJ, USA Req #448 Thursday, March 6, 2025 Looking for a chance to make a meaningful difference in the oncology ... is the role for you. Position Summary: + The Associate Director , Product Development will be responsible...cross-functional project teams and work closely with Quality Assurance, Regulatory as well as external Contract Organizations to ensure… more
- J&J Family of Companies (Raritan, NJ)
- …will be considered as a single submission. We are currently seeking an Associate Director , Global Labeling Product Leader. This position can be located ... in Raritan, NJ; Titusville, NJ; or Horsham, PA. The Associate Director , Global Labeling Product Leader will...required. + A minimum of 6 years of direct regulatory labeling content experience developing and writing … more
- Bristol Myers Squibb (Summit, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director , Therapeutic Area Audit Strategy Lead will be ... inspections . + External engagement as needed with industry/trade/QA associations, regulatory agencies, vendors, and licensing partners as well as pharmaceutical… more
- Merck (Rahway, NJ)
- **Job Description** The Associate Director of Scientific Nomenclature and Reference Data is responsible for assigning accurate chemical nomenclature to small ... incumbent will play a pivotal role in meeting cross-divisional and regulatory requirements by their strong scientific background, excellent communications skills,… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …designs at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre-specified product profile. - CRO / Vendor ... Health Authorities globally by providing input for the interaction or by writing the interaction document. May participate in meeting or teleconferences with Health… more
- Merck (Rahway, NJ)
- …modeling, Quality by Design (QbD) and Lean Six Sigma principles. + Experience supporting/ writing regulatory filings (IND, MAA, BLA) and inspections with multiple ... manufacturing sites, manufacturing investigations, process validation, and authoring of regulatory submissions. Under the general scientific and administrative direction… more
- Actalent (Morristown, NJ)
- Job Title: QA AssociateJob Description The QA Associate Operations of 3rd Party Quality reports to the Sr. Director , 3rd Party US Quality. This position supports ... client's commercial business and works closely with Supply Chain, Project Management, Regulatory Affairs, R&D, and external suppliers and partners. The position has… more