- ThermoFisher Scientific (Wilmington, DE)
- …(Days) **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards **Job Description** Thermo Fisher's clinical research ... a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. The scientist will perform a variety of routine to complex sample preparation… more
- ManpowerGroup (West Point, PA)
- **Job Title: Scientist - I** **Duration:** 12 Month Contract **Location:** Onsite - 770 Sumneytown Pike, West Point, PA 19486 **Hours:** **3rd shift (12 AM to 8 AM) ... and cell biology techniques. + Experience in laboratory operations including GMP documentation, equipment maintenance, and scheduling. + **Experience with cell… more
- dsm-firmenich (Exton, PA)
- **Analytical Associate Scientist ** **Exton, PA** The Analytical Associate Scientist will assure that dsm-firmenich Biomedical products are of consistent and high ... manufacturing of medical device materials, products or technologies in compliance with GMP and ISO standards and participating on project teams consisting of R&D,… more
- Merck (West Point, PA)
- …and authoring of regulatory submissions. **Job Description:** The Senior Scientist /Engineer will contribute to commercialization activities of late-stage pipeline ... studies and/or on-site activities related to tech transfer and manufacturing. GMP tasks include authoring, reviewing, and approving technical and regulatory… more
- Merck (West Point, PA)
- …Development (VDPD), a part of our company's Research Laboratories, is seeking a Principal Scientist to join our department in West Point, PA. Our mission is to ... + Ability to develop and implement new methods/processes + Experience with GMP manufacturing of clinical supplies + Experience with use of statistical principles… more
- Eurofins (Malvern, PA)
- …with requirements set forth by the department in electronic notebooks. * Apply GMP /GLP in all areas of responsibility, as appropriate * Provide training for other ... (chemistry, pharmacy or equivalent sciences degree) + Prior work experience in a GMP laboratory Experience with protein analytics, including, but not limited to are… more
- Eurofins (West Point, PA)
- …Chemistry, Biochemistry, or related scientific field + At least one year of GMP laboratory experience + Experience with HPLC, SDS Page, Dialysis, and similar assays ... + Experience following Standard Operating Procedures (SOP) and recording work in a lab notebook following Good Documentation Practices (GDP) + Authorization to work in the United States indefinitely Preferred Experience and Skills: + Experience with deviation… more
- Merck (West Point, PA)
- …area interdependencies, including upstream, analytical, and secondary manufacturing and GMP site readiness. + Actively interacts with internal and external ... counterparts. Represents functional area on cross-functional and cross-divisional teams. + Authors required regulatory and technical documentation. Ensures that processes are developed and documented according to standard of our Company practices. **Education… more
- Eurofins (Exton, PA)
- …in a scientific discipline + Minimum 10 years of Quality Control experience in GMP environment in the biologics industry, with a minimum of 3 years direct management ... experience in Quality Control + Excellent knowledge of cGMP guidelines, USP/NF, 21 CFR Parts 210 and 211, 600, 21 CFR Part 11, and other regulatory standards + Writing experience in a similar role in the biologics or pharmaceutical industry + Experience in… more
- Eurofins (Exton, PA)
- …chemistry, or similar scientific discipline + 3+ years in a quality control GMP environment specifically working on Flow Cytometry methodology in a similar role in ... the biologics industry + 2+ years of mammalian cell culture in an academic or industrial laboratory + Knowledge of Current Good Manufacturing Practice, Good Documentation Practices, and Industry standards required + Familiarity with analytical equipment such… more
- Eurofins (Exton, PA)
- …chemistry, or similar scientific discipline + 3+ years Quality Control experience in GMP environment specifically working on ELISA methodology in a similar role in ... the biologics industry + 2+ years' experience in mammalian cell culture in an academic or industrial laboratory + Knowledge of basic laboratory skills (including aseptic technique, pipetting, biohazard control) + Knowledge of Current Good Manufacturing… more