Provides guidance, training, and mentoring to PBF staff regarding cGMP documentation and quality systems. GMP QA Document Control Specialist. PBF is a..Share
Assists QA management in processing, reviewing, and maintaining SOPs, Forms, Batch Production Records (BPRs), trending charts, and other cGMP document..Share
PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next-generation development for cutting-edge companies and gov..Share
PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next-generation development for cutting-edge companies and gov..Share
Posted 3 weeks ago
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Maintain a full-time on-site presence to observe GMP manufacturing operations from material staging through final fill-finish • Monitor complian..Share
Description Your Role: The role is responsible for supporting implementation and maintenance of the GMP Training program to ensure compliance with all..Share
The GMP Cleaner is responsible for maintaining a clean working environment that meets the standards of (GMP) Good Manufacturing Practices. Works in pr..Share
Your Role: The role is responsible for supporting implementation and maintenance of the GMP Training program to ensure compliance with all relevant re..Share
life insurance, paid time off, paid holidays, sick time, tuition reimbursement, 401(k), retirement plan Join one of the largest bottlers and distribut..Share
Job Description R.D. Laboratories is a contract testing laboratory specializing in analytical analysis for the pharmaceutical industry. Applicants wil..Share
JOB SUMMARYThe Supervisor, Manufacturing, GMP Cleaning and Sanitization is responsible for supervising and ensuring the thorough and compliant executi..Share
Knowledge of GMP and non-GMP documentation requirements. Archive and maintain GLP and GMP documents with an accurate inventory, both on and offsite. Share