- Astrix Technology (Los Angeles, CA)
- …DOE **Location:** LA County, CA **Job type:** 6-month contract -to-hire **Schedule:** Monday-Friday 7:30am-4:30pm **Position Overview** The Manufacturing Engineer ... role ensures the facility operates safely, efficiently, and in compliance with relevant regulations. Responsibilities include managing building systems, coordinating… more
- Cambrex High Point (Minneapolis, MN)
- …Information You Matter to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development ... transfer analytical methods for APIs, API intermediates and raw materials. Strict compliance with cGMP guidelines is required to perform most job tasks.… more
- Specialty Rx, Inc. (Columbus, OH)
- …expenses and recommend cost-saving initiatives + Review vendor invoices for accuracy and contract compliance + Research and recommend new vendors for improved ... Technician Our Company: SpecialtyRx is a Long-Term Care pharmacy providing pharmaceutical services to long-term care facilities and assisted living communities. We… more
- Aerotek (Parsippany, NJ)
- …projects and upon completion. Construction and remodeling work is reviewed for compliance with specifications and building codes, and work is performed under general ... Construction software, written job requests, and emergency calls. + Ensure compliance with specifications and building codes during construction and remodeling… more
- Catalent Pharma Solutions (Winchester, KY)
- **Production Supervisor** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to ... a Patient First culture through excellence in quality and compliance , and to the safety of every patient, consumer...of Bachelors Degree. + 3+ years of experience in pharmaceutical manufacturing or a relative industry is required. +… more
- ThermoFisher Scientific (Wilmington, NC)
- …oversee the execution of select study/ies in assigned clinical program(s) in compliance with quality standards (including ICH GCP, local regulations and Takeda ... and/or other CROs + Oversee Strategic Partners/CRO/vendor selection, budget and contract negotiation, and proper supervision of performance for all activities… more
- Actalent (St. Louis, MO)
- …verification, and archival of batch records and associated documentation to ensure compliance with internal SOPs, cGMP, and FDA regulations. This role is primarily ... + Perform comprehensive batch record reviews for completeness, accuracy, and compliance with GDP and SOPs. + Review supporting documentation including logbooks,… more
- Actalent (St. Louis, MO)
- …You will manage and maintain the integrity of critical documents, ensuring compliance and efficiency within our operations. Responsibilities + Scan and archive batch ... accountability. + Document all activities to meet cGMP requirements. + Maintain cGMP compliance in assigned work and follow all safety procedures, including the use… more
- ThermoFisher Scientific (Boston, MA)
- …in the future. Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, ... you, the employee, to gain direct experience working onsite at a pharmaceutical / biopharmaceutical company, all while maintaining full-time benefits. This is a fully… more
- Boehringer Ingelheim (Fulton, MO)
- …the execution of a global development strategy for new pharmaceutical products (early research through regulatory submission). Independently operates, troubleshoots ... + Develop, validate, troubleshoots, modify and utilize methods in compliance with global regulatory requirements. + Independently operates, troubleshoots and… more