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- Planet Pharma is seeking a Purification Consultant to support cGMP manufacturing operations with responsibilities in execution and adherence to procedures. Ideal candidates will have a high school education or GED, with a preference for an AS/BS/BA in a science-related...Suggested
- ...Therapeutics, Inc. is seeking a Gowning Training Specialist in Raritan, New Jersey. This role involves conducting gowning training in a cGMP environment, ensuring compliance with quality and safety regulations. Responsibilities include executing training programs and...Suggested
- ...experience in a biologics/pharmaceutical. Experience developing and executing process, equipment, and validation protocols. Knowledge of cGMP practices and standards. Excellent written and verbal communication and interpersonal skills; prefer an individual with a positive,...SuggestedShift work
- An established industry player is seeking a dynamic Training Specialist to enhance organizational effectiveness through strategic training initiatives. This role involves conducting training needs analysis, designing impactful programs, and collaborating with various departments...Suggested
- A prestigious research institution in Chicago is seeking a candidate to support the documentation and reporting for clinical research efforts. This role involves environmental monitoring, equipment setup, and regulatory compliance within a cleanroom environment. The ideal...Suggested
- ...hiring a Biotechnician I in Hopewell, NJ to support the startup of their new manufacturing facility. The position involves executing cGMP operations and ensuring compliance with manufacturing protocols. Ideal candidates will have at least one year of experience in a...Suggested
- ...biotechnology firm is seeking a Quality Assurance Operations Specialist based in Philadelphia, PA. The role involves ensuring compliance with cGMP regulations, providing oversight during manufacturing, and reviewing batch records. Ideal candidates will hold a bachelor’s degree...SuggestedLong term contract
- ...seeking a Production Chemist in Torrance, CA to support the manufacture of high-quality Active Pharmaceutical Ingredients (APIs) in a cGMP-regulated environment. The role spans from executing batch production to maintaining compliance with safety and quality standards....Suggested
- Medium in Nashville, TN is seeking a Validation Supervisor to lead the validation team and manage validation projects in compliance with cGMPs. The ideal candidate will possess a BS in a relevant field and 6+ years of validation experience in the pharmaceutical or biotech...Suggested
- We are looking for a multiple Engineering resources to join our Life Sciences team to support major projects for various pharmaceutical clients in the Massachusetts and Southern NH areas (or other locations depending on interest). Ideal candidates should have a strong understanding...Suggested
- GREAT WHITE LABEL LLC is seeking an experienced Sanitation Technician for their cGMP-certified nutraceutical manufacturing facility in Ontario, California. This full-time, on-site role calls for a detail-oriented individual who can maintain clean production areas, crucial...SuggestedFull time
- ...intermediate-level role, the successful candidate will engage in complex laboratory activities adhering to prescribed processes, including CGMP and GLP guidelines. Key responsibilities include completing R&D work, conducting studies, ensuring data accuracy, and performing...Suggested
- Teva Pharmaceuticals is seeking an Investigator I to lead cGMP investigations in OSD manufacturing. This role involves coordinating quality and compliance efforts, root cause analysis, and corrective actions to ensure product quality. The ideal candidate holds a Master...Suggested
$83.68k - $115.06k
...California seeks a Production Coach to lead a manufacturing team. This role involves overseeing production stages, ensuring compliance with cGMP standards, and providing technical training and support. Candidates should have a degree in chemistry or biochemistry, and...Suggested- Concordance Healthcare Solutions, LLC in Edison, NJ is hiring a Quality Coordinator to support the cGMP compliant quality program. You will work with the management team to ensure regulatory adherence and maintain quality practices across distribution operations. The ideal...Suggested
- ...quality protocols within a fast-paced workplace. Applicants must have a high school diploma and preferably six months of experience in a cGMP setting. Strong problem-solving skills and attention to detail are key. The position offers opportunities for growth in a dynamic...
- ...Logics, Inc. is looking for a Site Quality Associate in Las Vegas, NV. The role involves ensuring compliance with quality programs in a cGMP-regulated environment. Responsibilities include coordinating quality programs, conducting audits, and maintaining documentation. The...
$37k - $60k
Pharmavite is seeking a Gummies Associate to support our manufacturing and warehouse operations in New Albany, Ohio. This role involves operating equipment and ensuring compliance with quality standards. Ideal candidates will possess a high school diploma and have some ...- Gift of Life Marrow Registry is seeking a Quality Assurance Coordinator based in Boca Raton, Florida. This role assists with oversight of the Quality Management System, ensuring compliance with federal and state regulations involving quality culture throughout the organization...Full timeFlexible hours
- Neier Inc. is seeking an MS&T Specialist - Deviations Investigator in Davie, FL. The role involves leading cGMP investigations, managing cross-functional collaboration, and ensuring compliance in OSD manufacturing. The ideal candidate will have a Master's or Ph.D. in a...
$87.58k - $92k
...Control (QC) Specialist to support manufacturing of biologics and cell and gene therapy products in its Good Manufacturing Practices (cGMP) facility. The role includes designing, developing, evaluating, and implementing quality control testing, assays, and procedures for...Full timeFixed term contract- Houston Methodist is looking for a Sr. Current Good Manufacturing Practices (cGMP) Specialist to ensure adherence to SOPs and cGMP regulations while overseeing compliance with quality operations. The role involves reviewing procedures, guiding team members, and contributing...
- ...seeking a qualified leader to oversee QA and QC operations in New Brunswick, New Jersey. The position requires ensuring compliance with cGMP standards and managing quality goals aligned with global objectives. Applicants should have a Bachelor's degree in a related field,...
- Guerbet is looking for a Warehouse Operations Lead in Raleigh, North Carolina. The role involves leading day-to-day warehouse operations in compliance with safety and quality standards, ensuring accurate handling of materials, and training warehouse associates. The ideal...
- Wedgewood is looking for a Quality Manager to manage quality assurance and control at their Albany facility. You will ensure high-quality execution of responsibilities and compliance with regulatory standards. The ideal candidate has over 10 years of experience in the biotech...Full time
$60.5k - $71.5k
A biopharmaceutical company in Cleveland is seeking a Specialist I in Quality Assurance to ensure compliance with cGMP guidelines and support manufacturing operations. The ideal candidate will hold a Bachelor's degree and have at least one year of experience in a regulated...- A leading IT staffing company is seeking a candidate with 0-3 years of GMP manufacturing or QA experience for a role in compliance and quality assurance. Responsibilities include ensuring adherence to regulatory requirements, coordinating batch records, and approving documents...
$131k - $165k
...disability, contact this employer to ask for an accommodation or an alternative application process. QMS Compliance Manager - IVD cGMP Full Time Fremont, CA, US 6 days ago Requisition ID: 1167 Salary Range: $131,000.00 to $165,000.00 Annually At Cytek Biosciences,...Full timeShift work- Houston Methodist is seeking a Sr. Current Good Manufacturing Practices (cGMP) Specialist in Houston, Texas. This role is vital in ensuring adherence to cGMP regulations and SOPs related to manufacturing therapeutics. Responsibilities include overseeing quality compliance...
- Hims, Inc. is seeking a Quality Control Specialist in Gilbert, Arizona, to enhance quality processes and ensure compliance with industry standards. The role involves conducting inspections and tests, maintaining product quality from manufacturing to delivery, and reporting...