| Job alert | Jobs 11 - 20 of 371 |
QC Analyst I
Piramal Pharma Solutions
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Sellersville, PA, 18960
... review Knowledgeable in compendial (USP/EU) testing requirements and ensuring compliance per FDA 21 CFR Qualifications Bachelor's degree in chemistry, biology, microbiology or other related science with relevant laboratory coursework is required. ... - Apr 22
Quality Assurance Manager
LHH
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Conshohocken, PA, 19429
... Responsibilities: Up-to-date understanding of FDA regulations, cGMP "Current Good Manufacturing Practice" and internal policies/procedures. Manage deviations, nonconformances, complaints, safety incidents, Corrective and Preventive Actions (CAPAs), ... - May 02
Validation Engineer - Life Sciences
Joulé
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Warminster, PA, 18974
... Responsibilities: Develop and execute validation protocols for pharmaceutical equipment, including systems and software validation, in accordance with regulatory requirements such as FDA, EU GMP, and ISO standards. Collaborate with cross-functional ... - May 02
Quality Assurance Manager
Extremity Care
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Conshohocken, PA, 19428
... Duties & Responsibilities: · Maintain a working knowledge of FDA 21 CFR 1271, FDA 21 CFR 820, AATB, other regulations (as appropriate), and industry standards. · Author, revise, and maintain procedures/controlled documents according to FDA, AATB, ... - Apr 25
Compounder (WKND)
Accupac
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Harleysville, PA, 19451
... In addition, the Compounder will ensure proper manufacturing operation is performed in a manner that complies with Accupac’s SOP and the FDA’s Good Manufacturing Practices Regulations. The Compounder’s level and compensation will be determined by ... - May 12
Senior Software Tester, Team Lead
YPrime
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Malvern, PA, 19355
... working in the biotech/pharmaceutical or CRO industries Demonstrated knowledge of the principles of SDLC Experience with FDA 21 CFR Part II requirements Experience reading Business Requirements Documents Here are some more details about the job: ... - May 06
Validation Engineer - Life Sciences
Joulé
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Warminster, PA, 18974
... Responsibilities: Develop and execute validation protocols for pharmaceutical equipment, including systems and software validation, in accordance with regulatory requirements such as FDA, EU GMP, and ISO standards. Collaborate with cross-functional ... - May 02
HCG Quality Engineer
Horizon Controls Group
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Philadelphia, PA, 19101
... Ensure Device History Records are maintained in compliance with FDA requirements. Metrics Management: Work with operating entities to establish and maintain procedures for inspection, process control, data analysis and product conformance. Issue ... - May 01
Manager - Microbiology Lab
Accupac
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Harleysville, PA, 19438
... Demonstrates strong knowledge of cGMP, ICH, FDA and compendial (USP, EP, JP) guidance. Strong knowledge of microbiological test methodology, environmental monitoring and industry-standard investigation process of any OOS that are related to ... - May 11
Regulatory Manager, Advertising & Promotion
CSL Behring
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King of Prussia, PA, 19406
... Review or reject promotional programming based on US Code of Federal Regulations, FDA's implementing regulations and guidelines established by Health Canada. Follow related SOPs and work instructions for established internal processes. Review ... - Apr 25