- 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
- Belcan (San Diego, CA)
- …all work carried out and equipment installed is safe, effective and in compliance with the appropriate industry standards. * Ensure all work undertaken is reflected ... group operations perspective) - Quality (who approve documents from a regulatory compliance standpoint) * Lead the execution of qualification protocols on process,… more
- Actalent (Englewood, CO)
- …compounding/clean room areas and related equipment are cleaned, sanitized and maintained in compliance with company policies and procedures, and USP 797 and USP 800 ... and humidity monitors, records all sterility testing done in the clean room in compliance with company policies and procedures, and USP 797 and USP 800 standards +… more
- PCI Pharma Services (Rockford, IL)
- …activities associated with medical device assembly lines within a fast-paced Contract Development and Manufacturing Organization (CDMO). The ideal candidate will ... lead equipment, process, and cleaning validation efforts to ensure compliance with FDA, ISO 13485, and other applicable regulatory standards. This role is critical… more
- Astrix Technology (Champaign, IL)
- …laboratory that partners with leading supplement, cosmetic, food, and pharmaceutical companies, providing industry-leading analytical services. **Type:** Contract ... + Perform testing for the food and nutrition supplement industries in compliance with cGMP, ISO standards, and company procedures, ensuring accurate results, timely… more