- J&J Family of Companies (New Brunswick, NJ)
- External Manufacturing Compliance Principal - 2406215428W **Description** Janssen Supply Group, LLC. is recruiting for an ** External Manufacturing ... Compliance Principal is accountable for regulatory compliance oversight of External Manufacturers within the...prepare, manage, and respond to health authority inspections at external manufacturing sites, support external … more
- Merck (Rahway, NJ)
- **Job Description** ** Principal Scientist / Director, GLOBAL REGULATORY CMC Biologics (R5)** Under general supervision of an Executive Director/Senior Director, the ... Principal Scientist /Director is responsible for developing and implementing...Scientist /Director is responsible for developing and implementing Chemistry, Manufacturing , and Controls (CMC) regulatory strategies for our organization's… more
- Catalent Pharma Solutions (Hillside, NJ)
- ** Principal Scientist, DMPK Advisory Services** **Position Summary:** Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical ... industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …device development, marketing, supply chain, global procurement, logistics, internal and external manufacturing sites, to successfully develop, tech transfer and ... primary packaging related regulatory filings pre and post approval. + Supports Manufacturing sites, Procurement, Global Quality and Compliance in supplier,… more
- Merck (Rahway, NJ)
- **Job Description** **Position Description:** **Associate Principal Scientist, Statistical Programming** The Associate Principal Scientist, Clinical Trial ... of focus include: + the assurance of deliverable quality and process compliance , + effective deliverable development utilizing global and TA standards that optimize… more
- Merck (Rahway, NJ)
- …**Position Description:** **Early Device Program Strategy and Due Diligence** The Principal Scientist of Early Device Program Monitoring & Due Diligence will ... selection, clinical evaluation, early combination product development, and regulatory compliance . **Position Qualifications** **:** **Education Minimum Requirement:** + Bachelor's… more
- Boehringer Ingelheim (New Brunswick, NJ)
- …to deliver fully-functional deliverables / projects meeting Customer requirements + Ensure compliance to regulatory requirements and BI / external standards ... decisions on new technologies to support future definition of innovative manufacturing platforms + Lead development, maintenance and advancement of technical body… more
- Merck (Rahway, NJ)
- …methodologies and tools to enable the discovery, development, regulatory approval, manufacturing , and marketing of medical drugs and vaccines for the benefit ... + Demonstrated success in the assurance of deliverable quality and process compliance . + Strategic thinking - ability to turn strategy into tactical activities;… more
- Merck (Rahway, NJ)
- …methodologies and tools to enable the discovery, development, regulatory approval, manufacturing , and marketing of medical drugs and vaccines for the benefit ... + Demonstrated success in the assurance of deliverable quality and process compliance . + Familiarity with statistics and clinical data management concepts. … more
- Merck (Rahway, NJ)
- …consolidated financial results in accordance with US Generally Accepted Accounting Principal (GAAP). The candidate will coordinate and prepare the financial data ... Assist with the preparation of our Company's US Generally Accepted Accounting Principal (GAAP) Consolidated Income Statement, Balance Sheet, Cash Flow Statement and… more
- MTA (New York, NY)
- …additionally responsible for the annual review of DBE certified firms for compliance with certification eligibility criteria and assisting in the management of the ... applications are processed within 90 days by Managers in compliance with the federal regulatory requirements of 49 CFR...+ Conduct a site visit to the applicant firms principal place of business for each new applicant firm,… more
- MTA (New York, NY)
- …additionally responsible for the annual review of DBE certified firms for compliance with certification eligibility criteria and assisting in the management of the ... the MTA, to gather information relative to the applicant's compliance with certification eligibility criteria as set forth in...submitted documentation. + Conduct an on-site review of the principal place of business for each new applicant, as… more