- United Therapeutics (Research Triangle Park, NC)
- … Management principles + 5+ years of experience in managing Quality Management Systems/Records in PV in the pharmaceutical industry + 5+ years of ... we are** We are the first publicly-traded biotech or pharmaceutical company to take the form of a public...about pharmacovigilance! You are a team player who loves quality , compliance, finding solutions and ensuring training standards are… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- … Pharmaceutical Sciences, or equivalent Experience: Minimum 3 years in Quality Assurance in the pharmaceutical , biopharmaceutical, or medical device industry, ... Quality Compliance Specialist Department: Quality Location:...well-positioned to successfully emerge as a leading integrated research-based pharmaceutical company. POSITION SUMMARY: Under the direction of the… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …Pharmaceutical Sciences, or equivalent Experience: + Minimum 3 years in Quality Assurance in the pharmaceutical , biopharmaceutical, or medical device ... Quality Systems Specialist Department: Quality Plant... Events, Deviations, Corrective and Preventative actions, QMR, Risk Management . This individual works closely with cross-functional teams at… more
- Kelly Services (Wilson, NC)
- …engineering, or technical discipline. + 3+ years of document control or records management experience within the pharmaceutical or biologics industry. + Strong ... **Now Hiring:** Quality Documentation Specialist (Coordinator 2 - Document Control)...exciting opportunity to work onsite in a dynamic, mission-driven pharmaceutical /biotech setting. **What You'll Do** In this role, you… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …but is not limited to, the following systems: Document Control, Electronic Quality Management Systems (Investigation, Change Control, CAPA) and Annual Product ... or relevant science degree Knowledge and Skill: 15-25 years in Pharmaceutical Industry - Investigations, Sterile Manufacturing Quality Assurance, Validation… more
- ThermoFisher Scientific (Greenville, NC)
- …+ Conduct quality risk assessments, and takes appropriate actions during quality system management and oversight activities (eg during review/approval) to ... cGMP experience and leadership required. + Deep knowledge of cGMPs and pharmaceutical contract manufacturing, Quality Assurance, Compliance, Quality Control… more
- Lilly (Durham, NC)
- …+ Resolve or escalate any compliance issues to the project, site, and Quality Management . **Minimum Requirements:** + Bachelor's degree in a science, ... Quality Systems, Engineering Technical Center, Global Parenteral Program, Pharmaceutical Delivery Systems, Global Packaging and Sterility Assurance Hub as… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- Senior Quality Control Analyst Department: Chemistry Location: Monroe, NC START YOUR APPLICATION ... position is for a highly motivated member of the Quality Control (QC) Lab at the Monroe manufacturing facility,...team responsible for drug product development and support to management , as necessary + Domestic and international travel up… more
- Lilly (Concord, NC)
- …resolution. In addition, this role will serve as the site steward for One Quality Management System (One QMS) during the project phase. Key Responsibilities: ... and investigation metrics. One QMS Responsibilities + Manage the transition of the Quality Management System (QMS) from TrackWise to Veeva for the Concord… more
- Otsuka America Pharmaceutical Inc. (Raleigh, NC)
- …and motivate others. **Qualifications** Required + Experience working within the pharmaceutical industry within data operations/data management environments. + ... **Job Summary** The Associate Director (AD), Commercial Data Management (CDM) within Data Enablement (DE) for Business...data sources. + Work closely with the DE Data Quality & Standards capability to apply quality … more