- AbbVie (North Chicago, IL)
- …on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Senior Manager Regulatory Affairs , Chemistry, Manufacturing and Controls (CMC) ... Preferred Experience: 10 years pharmaceutical experience including 5-plus years in regulatory affairs or 5-plus years in Discovery, R&D, or Manufacturing. +… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …as other research areas centered around rare diseases and immune disorders. **Summary** The Manager , Regulatory Affairs - Regulatory Project Management ... is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address...provides planning and coordination supports for global and US regulatory activities. The Manager RPM is responsible… more
- United Therapeutics (Silver Spring, MD)
- …and pulmonary diseases, and other orphan diseases. **How you'll contribute** The Senior Regulatory Affairs Manager partners with senior regulatory ... regulatory experience in pharmaceutical /biotech industry with PhD/PharmD/MD + Regulatory Affairs Certifications (RAC)-RAPS The salary for this position… more
- Chiesi (Cary, NC)
- Global Regulatory Affairs Manager Date: Nov 25, 2024 Department: Global Regulatory Affairs Job Type: Direct Employee Team: R&D, Pharmacovigilance & ... Regulatory Affairs Contract Type: Permanent Location: Cary,...one of us is Chiesi." **Purpose** The Global RA Manager supports the Global Regulatory Teams in… more
- BeiGene (San Mateo, CA)
- …Skills:** Microsoft 360 **Other Qualifications:** + 7+ years of related pharmaceutical or biopharmaceutical industry regulatory CMC experience with proven ... **General Description:** BeiGene is seeking an experienced and energetic regulatory professional to manage, evaluate, and complete regulatory projects consistent… more
- Amgen (Washington, DC)
- …over 10 million patients worldwide. It's time for a career you can be proud of. ** Regulatory Affairs Senior Manager - Regional Regulatory Lead** **Live** ... do** Let's do this. Let's change the world. The Regulatory Affairs Senior Manager at...Qualifications:** Doctorate degree and 2 years of experience in regulatory or pharmaceutical drug development Or Master's… more
- AbbVie (North Chicago, IL)
- …will be added to our talent pipeline and considered for future opportunities. Global Regulatory Affairs Strategy roles (US and Canada) are: 1. Responsible for ... , R&D, or Industry-related experience is required. 2-3 years in pharmaceutical regulatory activities is preferred. + Demonstrates excellent negotiation… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- Support CMC development activities from a regulatory standpoint during early phase, development, submissions and post market requirements for gene therapies. **A ... in cross-functional meetings for program-specific discussions, proactively identify CMC regulatory issues and suggest appropriate strategies to mitigate risks +… more
- Envista Holdings Corporation (Brea, CA)
- …its Quality Systems. + Prepares monthly reports on status of current issues to the Manager of Regulatory Affairs . + Work on ad-hoc projects when required. ... **Job Description:** **JOB SUMMARY:** The Regulatory Affairs Specialist is responsible for...work experience required, preferably in the Medical Device or Pharmaceutical industry or technical field. + Ability to understand… more
- ManpowerGroup (Schenectady, NY)
- Our client in the pharmaceutical industry is seeking a Regulatory Affairs Project Specialist to join their team. As a Regulatory Affairs Project ... Specialist, you will be part of the regulatory affairs team supporting the Carve-out project...for me?** + Opportunity to work with a leading pharmaceutical company in the industry. + Remote work option.… more
- Actalent (Union, MO)
- Job Title: Regulatory Affairs Project SpecialistJob Description The Regulatory Affairs Project Specialist will play a crucial role in supporting the ... regulatory affairs team during the Carve-out project...documentation and regulatory adherence. + Familiarity with regulatory documents in the food industry, pharmaceutical ,… more
- University of Pennsylvania (Philadelphia, PA)
- …approvals and associated site initiation documentation. Reporting to the Regulatory Affairs New Study & Continuing Review Manager , the Regulatory ... trials that offer cutting-edge oncology treatments. Contingent upon funding. The CRU OCCR Regulatory Affairs Office seeks a full-time Regulatory Affairs… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …Job Overview** The Senior Manager , Public Policy in International Government and Regulatory Affairs (IGRA) is an integral position within a global team of ... public policy and regulatory affairs experts. The candidate will play...the policy content generated and managed by the Senior Manager will be utilized in dialogues with policy makers… more
- Takeda Pharmaceuticals (Lexington, MA)
- …+ 10+ years of overall biopharmaceutical/device industry experience with 8+ years pharmaceutical Regulatory CMC and / or devices experience, while leading ... assigned products as GRA CMC Product Lead. Represents and contributes to Regulatory , Pharmaceutical Development, and Commercial project teams throughout clinical… more
- Takeda Pharmaceuticals (Boston, MA)
- …and be empowered to deliver your best. As part of the Global Medical Affairs Oncology team, you will report to the Head of Evidence Generation, Global Medical ... Affairs Oncology. You will work cross-functionally with but not...cross-functionally with but not limited to Clinical Operations, Legal, Regulatory , Procurement, Patient Value Access and Safety. + Provides… more
- Takeda Pharmaceuticals (Lexington, MA)
- …my knowledge. **Job Description** **Senior Manager , US Medical Ad/Promo Regulatory Review** **Takeda Pharmaceutical ** **Lexington, MA or Exton, PA** **About ... the role:** Join Takeda as a Senior Manager , US Medical Ad/Promo Regulatory Review where...potential issues. **POSITION ACCOUNTABILITIES:** + Collaborate with colleagues in Regulatory Affairs , Medical, Legal, Commercial, and Compliance… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …point of contact for cross-functional teams, including R&D, clinical operations, regulatory affairs , quality assurance, and marketing. + Facilitate communication ... Senior Project Manager , External Manufacturing & Supply Organization Date: Oct...Lead the planning, execution, and delivery of multiple large-scale pharmaceutical projects, including drug development, and regulatory … more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Regulatory Affairs Labeling Operations Fellowship is designed to provide pharmacists with exposure to regulatory requirements for US ... opportunity to complete rotations in areas within and beyond Regulatory Affairs . This position will require the...to contribute to their respective functional area within a pharmaceutical company. The Fellow will be based at Boehringer… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Regulatory Affairs Labeling Content Fellowship is designed to provide pharmacists with exposure to regulatory requirements for US product ... opportunity to complete rotations in areas within and beyond Regulatory Affairs . This position will require the...to contribute to their respective functional area within a pharmaceutical company. The Fellow will be based at Boehringer… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and document policies and procedures within the CMC regulatory affairs department under supervision of manager . Participates in initiatives internal ... regulatory affairs ; or Bachelor's Degree with 5+ years of pharmaceutical CMC regulatory related experience. + Degree in Pharmacy, Biology, Chemistry,… more
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