- Daiichi Sankyo, Inc. (Bernards, NJ)
- …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 & Co. (Rahway, NJ)
- Job DescriptionThe 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
- Legend Biotech USA, Inc. (Raritan, NJ)
- Legend Biotech is seeking Associate Technical Lead as part of the Technical Operations team based in Raritan, NJ. Role OverviewThe Associate Technical Lead will ... Responsibilities This individual with provide direct support to the Director of Manufacturing Excellence by providing technical expertise to Technical… more
- Merck & Co. (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
- 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
- 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
- PSEG (Newark, NJ)
- …as the attention, camaraderie, and care for one another you might typically associate with a small business. Our focus on combatting climate change through clean ... internal controls and maintenance of tax accounting related databases. In addition, the Director - Tax Accounting and Reporting collaborates with the Director of… 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
- PSEG (Newark, NJ)
- …as the attention, camaraderie, and care for one another you might typically associate with a small business. Our focus on combatting climate change through clean ... including setting Board meeting agendas, working with the PEGPAC director to create the PEGPAC budget and manage all...working across the Enterprise to create timely and accurate regulatory compliance filings at the state and federal levels;… more
