- Astrix Technology (New Brunswick, NJ)
- **Mircobiology Manager ** Laboratory Middlesex County, NJ, US Pay Rate Low: 48 | Pay Rate High: 50 + Added - 24/06/2025 Apply for Job Our client, a dynamic ... with a global footprint in both R&D and manufacturing, is seeking a Microbiology Manager to join their growing team on a contract to hire basis. **Job Title:**… more
- West Pharmaceutical Services (Williamsport, PA)
- Process Engineering Manager Requisition ID: 70704 Date: Jul 16, 2025 Location: Williamsport, Pennsylvania, US Department: Operations Description: At West, we're a ... planet through our sustainability efforts. **Job Summary** The Process Engineering Manager will lead the engineering team responsible for developing, optimizing, and… more
- Dr. Reddy's Laboratories (Princeton, NJ)
- …issues, Laboratory and Manufacturing investigations, Product Specifications, Analytical Method Validation , Process Validation , Method and process Transfer and ... data. + Reviews Analytical method and process development, enhancements and validation /verification, transfer related documents and raw data generated at DRL… more
- AbbVie (Worcester, MA)
- …influencing quality on a global scale. + Oversee the development and validation of analytical methods for new product introductions (NPIs), ensuring they meet ... Data Integrity: + Ensure the integrity and accuracy of raw data used in validation processes and Test Method Transfers (TMTs) within our global network of Quality… more
- VTI Life Sciences (Los Angeles, CA)
- …excellence by providing Commissioning, Qualification, Quality Engineering, Automation and Validation Services to the Pharmaceutical , Biotechnology, Biologics and ... and ambitious engineers looking to accelerate their career in the pharmaceutical , biotechnology and medical device industries. We offer an opportunity to… more
- Element Materials Technology (North Liberty, IA)
- **Overview** Element Iowa City has a current opening for an **IT Manager ** to join our growing team. The **IT Manager ** provides strategic and operational ... regulated environment. This includes managing the continued development and validation of the organization's custom Laboratory Information Management Systems (LIMS)… more
- Cambrex High Point (Longmont, CO)
- …world. Start a career where You Matter by applying today! Job Overview The Manager of Quality Assurance is responsible for the daily operations of the Quality ... are in compliance with company SOPs, cGMP/cGLP standards and FDA/EU regulations. The Manager of Quality Assurance leads and mentors the quality team and is expected… more
- Fujifilm (Holly Springs, NC)
- **Position Overview** The Manager , QC Laboratory Information Management System (LIMS) is responsible for developing strategic plans for implementing FDB's global ... the transition of QC into a paperless environment. The Manager , QC LIMS guides a team of LIMS experts...the LIMS implementation process o Develop, implement,, and review validation protocols, SOPs, test scripts, and training materials for… more
- Gilead Sciences, Inc. (Foster City, CA)
- …GxP, FDA, EMA, and other regulatory bodies. + Lead the development of validation strategies and documentation to support compliance efforts. **Integration with SAP & ... FDA 21 CFR Part 11, and other applicable standards. + Partner with Validation teams to develop and maintain validation documentation, including validation… more
- AbbVie (North Chicago, IL)
- …internal partners to establish best in class practices for risk management, validation and other related Quality Systems for pharmaceutical products, biologics, ... Risk Management (QRM) activities for AbbVie products such as Combination, Pharmaceutical and medical devices. Support the strategic direction to ensure business… more
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