- CBRE (Concord, NC)
- Quality & Compliance Manager - Pharmaceutical Manufacturing Job ID 182517 Posted 05-Sep-2024 Service line GWS Segment Role type Full-time Areas of Interest ... have appropriate license and/or certification where required by law. Must hold Quality in Pharmaceutical Manufacturing environment. **Why CBRE?** At CBRE, we… more
- Procter & Gamble (Greensboro, NC)
- …Quality Assurance Manager to lead a team responsible for end-to-end quality assurance in our pharmaceutical & dietary supplement manufacturing facility in ... Job Location Greensboro Job Description P&G Manufacturing is all about safety, quality , and productivity. It's where our products are packaged and palleted, ready to… more
- Belcan (Berkeley, CA)
- Project Manager - Pharmaceutical Conformance Job Number: 353354 Category: Project Management Description: Job Title: Project Manager - Pharmaceutical ... of experience in a related field such as: Engineering, Quality , or Manufacturing in the pharmaceutical industry...Werum Pas-X) * Risk Assessments * Authoring/Reviewing Documents for Regulatory Review * Lean Six Sigma and Continuous Improvement… more
- Catalent Pharma Solutions (Kansas City, MO)
- …Associate Pharmaceutical Technician. At the direction of the Zone Operations Manager or Pharmaceutical Manufacturing Lead, the Associate Pharmaceutical ... **Associate Pharmaceutical Technician** **Position Summary** Catalent is a global,...adhering to policies and procedures with an emphasis on regulatory related processes such as SOPs, cGMP and safety… more
- American Institutes for Research (Rockville, MD)
- …a Project Manager or Project Director). + Review and interpret regulatory and sub- regulatory guidance. May include, interpreting policy and regulation. + ... is seeking a confident, self-motivated, and creative **Medication and Pharmaceutical Policy Analyst** to join ourHealth (https://www.air.org/our-work/health) team to… more
- MD Anderson Cancer Center (Houston, TX)
- …with the research team and Principal Investigator (PI) to coordinate clinical trial quality assurance, submission and regulatory process for the departmental. To ... The primary purpose of the Manager , Clinical Protocol Administration position is to collaborate...trial inspection readiness. To provide leadership and supervision of Regulatory and Quality Assurance (QA) team ensuring… more
- Chiesi (Cary, NC)
- Global Regulatory Affairs Manager Date: Nov 25, 2024 Department: Global Regulatory Affairs Job Type: Direct Employee Team: R&D, Pharmacovigilance & ... (Chiesi Group). To achieve its mission of improving people's quality of life by acting responsibly towards society and...one of us is Chiesi." **Purpose** The Global RA Manager supports the Global Regulatory Teams in… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders. **Summary** The Manager , Regulatory Affairs - Regulatory Project Management (RPM) ... 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
- 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
- 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 in North...for me?** + Opportunity to work with a leading pharmaceutical company in the industry. + Remote work option.… more
- Amgen (Washington, DC)
- …team. Join us and transform the lives of patients while transforming your career. ** Regulatory Labeling Manager ** **What you will do** Let's do this. Let's ... Labeling (GL), and under the supervision of the Therapeutic Area Lead, the Regulatory Labeling Manager is responsible for supporting the facilitation and… more
- Mount Sinai Health System (New York, NY)
- …QA ( Quality Assurance) program for order verification and comprehensive pharmaceutical care. * Oversees all aspects of medication-related policies and procedures ... **Job Description** Responsible for all regulatory and compliance related activities, coordination, record keeping and presentation for all of the facilities within… more
- AbbVie (North Chicago, IL)
- …, R&D, or Industry-related experience is required. 2-3 years in pharmaceutical regulatory activities is preferred. + Demonstrates excellent negotiation ... with regulations, company policies, procedures, & guidance in alignment with regulatory product strategy & Quality Dossier Program (QDP). Qualifications… more
- Olympus Corporation of the Americas (Westborough, MA)
- …and coordinating compliance response communications working cross functionally with Market Quality , Marketing, Operations/Ops Quality , Regulatory , Risk and ... good working relationships with all Olympus locations and internal departments (Market Quality , Marketing, Manufacturing, Quality , Regulatory , Risk, R&D,… more
- Gilead Sciences, Inc. (Foster City, CA)
- … Affairs. We work collaboratively to advance the strategy and create high- quality documents for successful regulatory submissions, by bringing our passion ... quality review for a variety of clinical and regulatory documents. We are dedicated to attracting new talent...team, stakeholders, and vendors. + Engages with vendor business manager (s) and vendor staff as needed. May participate in… more
- West Pharmaceutical Services (Exton, PA)
- …guidance documents and current state-of-art standards/regulations. + Collaborate with regulatory lead(s), cross-functional project manager (s) and SMEs (Subject ... medical device use. + Ability to handle technical reports, drawings, specifications, regulatory and quality documentation with a high degree of confidentiality.… 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
- Boehringer Ingelheim (Ridgefield, CT)
- …and compliance issues, ensuring that documents meet the highest standards of quality and compliance. * Coordinate and prepare regulatory labeling documents ... **Description** The Regulatory Affairs Labeling Operations Fellowship is designed to...to contribute to their respective functional area within a pharmaceutical company. The Fellow will be based at Boehringer… more
- University of Washington (Seattle, WA)
- …well as ensure compliance with the SOPs/guidelines. This position may also perform Quality Assurance checks on regulatory files as needed and implement/maintain ... of Medicine: Hematology and Oncology has an outstanding opportunity for Regulatory Coordinator.** **Position Purpose:** The University of Washington's Division of… more
- Gilead Sciences, Inc. (Foster City, CA)
- …the critical issues,negotiate, influence, and provide strategic advice to peers in Pharmaceutical Development and Manufacturing, RA, and Regulatory Operations. + ... support as required, analyzes and interprets information provided to facilitate informed regulatory decisions for submissions. + Author high quality global CMC… more