- AbbVie (Chicago, IL)
- …than problems as projects encounter the inevitable ups and downs associated with new drug development or on-market product support. Must be a self- starter and ... across all products within their TA portfolio integrates and aligns with the product strategy plans from matrix groups as well as commercial interests and scientific… more
- Teva Pharmaceuticals (West Chester, PA)
- …resources for medical writing support in clinical research documentation used in drug development and product registration. **Travel Requirements** : Up to ... of global regulatory guidelines and AMA style + Familiarity with drug development, therapeutic areas, and statistical concepts Job-Specific Competencies: + Excellent… more
- The Boeing Company (Charleston AFB, SC)
- …audiences and varying levels of the organizations/Military ranks to convey product design/repair design strategies. ** Drug Free Workplace** **:** Boeing ... is a Drug Free Workplace where post offer applicants and employees are subject to testing for marijuana, cocaine, opioids, amphetamines, PCP, and alcohol when criteria is met as outlined in our policies. **General** All information provided will be checked… more
- Rhythm Pharmaceuticals (Boston, MA)
- …in life sciences preferred + 8+ years of Regulatory Affairs experience in drug development and product registration activities within the pharmaceutical or ... (regulations, directives and guidance/guidelines) pertaining to the development and registration of drug products in multiple ICH regions + Evidence of being a… more
- Penn Medicine (Plainsboro, NJ)
- …State University of New Jersey. The Pharmacy staff provides all sterile intravenous product preparation and oral medications, drug information, and reviews all ... and regulatory agency requirements. Assists in the management of controlled drug substances, inventory and the procurement process **Benefits You'll Receive at… more
- Teva Pharmaceuticals (West Chester, PA)
- …medical-writing support in the production of clinical research documentation used in drug development and product registrations. The Director offers clear ... regulatory medical writing expertise, strong writing/editing skills, knowledge of drug development regulations + Global regulations and guidelines for document… more
- Penn Medicine (Philadelphia, PA)
- …purchasing and inventory issues including loaning/borrowing medications, managing blood factor product consignment, receipt of controlled drug orders and ... appropriatelyReview, evaluate, and approve or deny non-formulary requests when Drug Information services are unavailableAccess outpatient pharmacy after-hours as… more
- Sokol Materials & Services (Skillman, NJ)
- …Qualification and some project management experience. + Knowledge of biotech, bulk drug substance or finished product manufacturing, medical device analytical ... experience in a GMP, GCP, or GXP with at least 8 years focused on product quality. Preferred Active member of ASQ or ISPE. + Prior experience of QC equipment… more
- Ascendis Pharma (Princeton, NJ)
- …to the FDA's Advertising and Promotional Labeling Branch and Office of Prescription Drug Promotion for respective product (s) and will ensure materials are ... regulations, guidance, and enforcement trends governing the promotion of prescription drug and biologic products. The Senior Manager Regulatory Affairs, Advertising… more
- Sanofi Group (Framingham, MA)
- …Excellence** provides scientific expertise to accelerate technical modernization for product commercialization within the MSAT Recombinant Drug Substance ... with innovative approaches to process and analytical comparability, whilst supporting product technical teams to assess risk, probability of success and change… more