Join Total eQMS Management as a Biotech eQMS Entry-Level Contractor. Manage eQMS software, test solutions, author SOPs, and develop training materials. Prioritize tasks effectively and contribute to efficient, compliant solutions for biotech clients....
Join our team as a Quality Assurance Associate in Albany, OR, for a 9-month contract. Assist in document management, audits, NCRs, CAPAs, and data entry. Ensure document integrity and compliance while collaborating with the team. Bachelor's degree an...
Seeking a Biotech eQMS Entry-Level Contractor to manage software solutions, test and validate systems, draft SOPs, and develop training materials. Opportunity to advance in a dynamic organization focused on efficient and compliant eQMS solutions for ...
Seeking a seasoned Training Lead to spearhead the training program at Wheeler Bios. Ideal candidates will have a background in bioprocessing or pharma, strong regulatory knowledge, and experience in instructional design. Responsibilities include prog...
Seeking an Engineer for Biotech Process Equipment at a top biotech firm in Thousand Oaks, CA. Responsible for ensuring the reliability and compliance of manufacturing equipment while driving safety and quality. Supports capital projects and fosters a...
Join a Biotech Company in Exton, PA as a QA Specialist. Review manufacturing records, manage batch disposition, uphold quality standards, and support QA programs. Required: Bachelor's degree, 3-5 years in biotech/pharma QA, MasterControl familiarity....
Exciting role overseeing QA programs at a global industry giant's SC plant. Manage team, ensure compliance, quality, and standards in production. Drive continuous improvement, mock recalls, and HACCP program. 7-10 years QA exp in FDA, GMP, SAP enviro...
Join a rapidly growing Pharmaceutical Manufacturing company in Fort Worth, TX as their new Director of Quality Assurance. Lead a team in implementing top-tier quality systems for renowned pharma and biotech firms. Oversee audits, SOPs, and compliance...
Join Validated Cloud, a top Community Cloud for Life Science Regulated Systems. Seeking a meticulous Senior Quality Specialist in Waltham, MA. Requires 4+ years in pharma QA, adept in GxP, HIPAA, GDPR, 21 CFR Part 820, and 21 CFR Part 11. $90K/yr wit...
Join a top drug and medical device company as a Quality Assurance Specialist in Albany, OR. Manage document processes, audits, CAPAs, and deviations. Ideal candidates have a Science degree and 2-3 years' regulated industry experience. Enjoy great ben...
