- Quality Chemical Laboratories (Wilmington, NC)
- Quality Chemical Laboratories (QCL), a pharmaceutical testing, manufacturing, and development lab in Wilmington, is seeking a highly motivated scientist for our ... technology transfer into cGMP manufacturing, familiarity with analytical techniques, regulatory requirements, and early phase cGMP manufacturing is preferred. QCL… more
- Deloitte (Los Angeles, CA)
- …serve + Limited immigration sponsorship may be available Preferred: + Understanding of pharmaceutical regulatory data and regulatory filing requirements and ... analytics solutions + 4+ years of experience with Life Sciences Pharmaceutical R&D regulatory data lifecycle . Experience to include introducing new technologies… more
- Cardinal Health (Mansfield, MA)
- …ICH guidelines, FDA regulations, Data Integrity, Quality Risk Management and other pharmaceutical regulatory requirements, preferred. + Working knowledge of ... as LabWare. + Possesses significant working knowledge of USP, FDA and ICH regulatory requirements as applicable to pharmaceutical stability testing. + Possess a… more
- Takeda Pharmaceuticals (Boston, MA)
- …including Tetrascience, QbDVision, PAS-X, SAP or Databricks + Understanding of regulatory standards in pharmaceutical industry **Behavioral Competencies:** + ... to putting patients first. As the Director, Technology Business Partner for Pharmaceutical Sciences R&D Data Digital and Technology (R&D DDT), you will serve… more
- Takeda Pharmaceuticals (Boston, MA)
- …+ 10+ years of overall biopharmaceutical/device industry experience with 8+ years pharmaceutical Regulatory CMC and / or devices experience, while leading ... products as GRA CMC Product Lead. + Represents and contributes to Regulatory , Pharmaceutical Development, and Commercial project teams throughout clinical… more
- Cardinal Health (Helena, MT)
- …Standards + Drug, Biologic (IV, Injectable) and Medical Device Development + Regulatory Outsourcing + Pharmaceutical Compliance + Product Lifecycle Management + ... **Position Summary** For nearly five decades, Cardinal Health Regulatory Sciences' industry-trained regulatory consultants have provided expertise and guidance… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …Public Health, or related field. + 10+ years of experience in pharmaceutical stability, regulatory compliance, and product lifecycle management. + Proven ... record of developing stability testing protocols, managing stability data for regulatory submissions, and implementing automated systems for stability tracking and… more
- West Pharmaceutical Services (Exton, PA)
- …Bachelor's with 5+ years; Master's degree/PhD with 3+ years of medical device, pharmaceutical or regulatory experience **Work Experience** + Bachelor's with 5+ ... years of medical device, pharmaceutical or regulatory experience + Master's degree/PhD with 3+ years of medical device, pharmaceutical or regulatory … more
- Stryker (Trenton, NJ)
- …disposition and release in addition to Quality Assurance responsibilities.Viewed as pharmaceutical regulatory expert within business. + Leads communication with ... aspects in external agency audits/inspections. + Stays abreast of external pharmaceutical regulatory requirements and expectations. **Education & Special… more
- Taiho Oncology (Princeton, NJ)
- … requirements and submission processes. + In depth knowledge of global regulatory requirements for pharmaceutical development and manufacturing. + Strong working ... our dynamic and expanding mid-size company in the role of Director for Regulatory CMC directly reporting to Executive Director, Regulatory CMC. Your expertise… more
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