- The US Pharmacopeial Convention (USP) (Rockville, MD)
- **Description** ** Pharmaceutical Product Quality Testing (PPQT) Market and Demand Generation Consultancy** The **U.S. Pharmacopeial Convention (USP)** is an ... Africa, Asia, and South America, strengthening global supply chains and pharmaceutical ecosystems that enable a resilient supply of high-quality medical products.… more
- Actalent (Sanford, NC)
- …Description We are seeking a Quality Assurance Associate to support a major pharmaceutical client. The QA Associate will be responsible for real-time batch record ... review on the manufacturing shop floor, among other duties....a manufacturing facility. + At least 6 months of pharmaceutical quality experience. Additional Skills & Qualifications + Experience… more
- Catalent Pharma Solutions (Kansas City, MO)
- ** Pharmaceutical Packaging Technician II** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose ... Pharma Solutions in Kansas City, MO is hiring a Pharmaceutical Packaging Technician II. The Pharmaceutical Packaging...Join Catalent:** + Defined career path and annual performance review and feedback process + Diverse, inclusive culture +… more
- Cardinal Health (Charleston, WV)
- …Legal function. **_Job Summary_** The Assistant General Counsel - Specialty Pharmaceutical Distribution will be responsible for providing exceptional legal advice ... and guidance to the Specialty Pharmaceutical Distribution segment business clients. **_Responsibilities_** + Demonstrate strong...other status protected by federal, state or local law._ _To read and review this privacy notice click_ here… more
- Merck (Rahway, NJ)
- …for sterile operations under the remit of Our Company's Research Labs Pharmaceutical Sciences (Pharm Sci), Pharmaceutical Operations Engineering group (Pharm Ops ... Ops Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply (PSCS) The FLEx sterile...are suitable for both GMP and developmental use. Author, review and approve GMP procedures and documentation, with an… more
- Boehringer Ingelheim (Ridgefield, CT)
- …will play a pivotal role supporting Boehringer Ingelheim's US Human Pharmaceutical Business, particularly our Patient Excellence and Therapeutic Areas. Duties ... have acquired knowledge of law in at least two (2) specialized areas of pharmaceutical law, one of which must be FDA Regulatory (eg, patient support programs, market… more
- AbbVie (North Chicago, IL)
- …parameters or recipes. + Leads Execution of Risk Management. including, periodic review and update per the Validation Master Plan, interface with best practices, ... including overall program. Understands risk management principles. Can find and review documentation. Understands controls, impact of change, trace controls, and can… more
- PCI Pharma Services (Bedford, NH)
- …activities, and equipment maintenance + Directs personnel to complete and review all associated batch record and SOP documentation + Writes, reviews/approves ... with disabilities to perform the essential functions. + Proficiency in pharmaceutical process development for aseptically produced products or medical device… more
- PDS Tech Commercial, Inc. (Millburn, NJ)
- …Tech Commercial** , we're partnering with a leading name in ** Pharmaceutical Manufacturing** to deliver innovation and excellence in **Radioligand Therapy (RLT)** ... and clearly communicate findings and resolutions + Draft and review GMP-compliant manufacturing documentation **What You Bring:** **Required:** + Bachelor's… more
- Lilly (Indianapolis, IN)
- …around the world. **Position Brand Description:** The Assoc. Director - GQAAC GMP Pharmaceutical role is part of the Global Quality Auditing and Compliance (GQAAC) ... and regulatory compliance. The Assoc. Director - GQAAC GMP Pharmaceutical plays a key part in contributing to the...of audit plan + Ensure consistency between audits + Review and approve audit and assessment reports and summaries… more