Get new jobs by email
$100k - $199k
...deliver our broad portfolio of analytical solutions, and OneSource services. Job Title Senior/Manager, Automation Engineering (cGMP) - Project Farma Location(s) Boulder, CO, Boulder, CO, Cambridge, MA, Columbus, OH, Concord, NC, Customer Site - AL, Customer Site...SuggestedFull timeWork visa- ...support daily operations in a regulated environment. You will handle materials, label, store, stage, and ship goods while following cGMP and GDP guidelines to ensure product quality and accurate documentation. Responsibilities include operating PITs, performing ERP/SAP...Suggested
- ...warehouse associate to support daily operations in a regulated environment. You will handle, label, store, and ship materials in line with cGMP and GDP, with emphasis on accuracy and procedural discipline. The role involves operating PIT equipment, using SAP ERP and RF...Suggested
$39.95 - $45.24 per hour
...comprised of the faculty, students and staff that make the university what it is. USC's Keck School of Medicine, Department of Medicine - cGMP is seeking a dynamic facility coordinator for its cGMP facility. The coordinator will oversee all cGMP lab and ancillary space...SuggestedHourly payFor contractorsWork experience placementLocal area- ...materials to end users. This role collaborates with Supply Chain teams to ensure accurate receipt and processing of materials in support of cGMP compliance. The successful candidate will perform inventory transactions, maintain documentation, and help maintain warehouse...Suggested
- The University of Southern California (USC) seeks a dynamic Facility Coordinator for its cGMP facility within the Keck School of Medicine. You will oversee cGMP lab spaces, ensure compliant operations, and support the development of cell and gene therapies. Responsibilities...SuggestedFor contractors
$76k - $121.9k
...the path from lab to life while championing patients every step of the way. Learn more at We are searching for the best talent for cGMP Compliance and Investigations Lead to join our Innovative Medicine team in Spring House, PA. Purpose The cGMP Compliance and...SuggestedWork at officeLocal area- Renaissance Lakewood LLC in Lakewood Township, New Jersey, is seeking a capable production associate to perform assigned tasks safely and accurately in a pharmaceutical manufacturing setting. You will empty trash, sweep, mop, clean restrooms and locker rooms, replenish ...Suggested
- ...at the Marietta facility. The role focuses on calibration, validation, and ongoing equipment maintenance to ensure compliance with cGMP and regulatory standards. The ideal candidate has an Associate degree in engineering or science and at least two years in a medical...Suggested
- mycts seeks a Quality Specialist to ensure cGMP compliant lab testing processes and accurate final release of results to customers. Under supervision, you will apply standard procedures and contribute to performance improvement and data integrity. You will review QC data...Suggested
- AbbVie in the Chicago area seeks a Cleaning Specialist to support cGMP manufacturing with microbial control cleaning and strict documentation. You will prepare solutions, follow gowning procedures, and use various cleaning equipment in a regulated environment. Strong attention...Suggested
- ...LLC is seeking a Training and Development Coordinator to design, implement, and manage comprehensive training programs that ensure cGMP compliance and support employee growth across departments. Under the Director of Training and Development, you will standardize training...Suggested
- A prominent IT staffing company is seeking a Manufacturing Technician in Sanford, North Carolina. In this role, you will operate and maintain production equipment, ensure compliance with regulatory requirements, and clean facilities according to Good Manufacturing Practices...Suggested
- ...Biotec North America in Gaithersburg, MD is seeking a warehouse associate to perform routine inventory and material handling tasks in a cGMP environment. You will operate PITs, use SAP and RF systems, and ensure accurate data entry and documentation. You will pick, package...Suggested
- About the Role Catalent Pharma Solutions is seeking a Manufacturing Operator to support its pharmaceutical production operations in a cGMP-regulated environment . This role plays a critical part in ensuring high-quality softgel manufacturing, inspection, and packaging...SuggestedImmediate start
- Stokes Healthcare in Mount Laurel, NJ, seeks a labeling technician to operate in a cGMP environment under supervision of the Manufacturing Manager. You will perform labeling, packaging, and QA coordination, ensuring precision and timely results for both human and animal...
- ...perform all mixing and blending operations to ensure products are manufactured according to master manufacturing records, SOPs, and FDA cGMP standards. You will weigh, load, mix ingredients, monitor batch progress, ensure blend uniformity, and maintain a clean, compliant...
- Johnson & Johnson Innovative Medicine in Spring House, PA seeks a cGMP Compliance and Investigations Lead to drive deviation investigations and CAPA programs supporting cell therapy development and manufacturing. You will work across Manufacturing, QA, QC, and technical...
$42k - $46k
...level. Track schedule changes to proactively adjust label and documentation needs. Review batch records for completeness and cGMP compliance; compute product and label yields and investigate variances outside expected ranges. Guide plant personnel and Manufacturing...Temporary workWork at officeMonday to FridaySTERIS - Operations
Saint Louis, MO3 days ago- PolyPeptide Laboratories Torrance, CA is seeking a Production Chemist I-III to support peptide manufacturing in a cGMP environment. You will work across upstream synthesis and downstream purification, ensuring quality and compliance while contributing to manufacturing...
- Miltenyi Biotec, Inc. is seeking an entry-level manufacturing staff to support biologics production in a cGMP facility in Gaithersburg. This role follows established SOPs, performs batch records, and adheres to gowning procedures for cleanroom work. The position requires...
- ...will operate inspection equipment, perform visual and physical inspections, and ensure accurate batch documentation while maintaining cGMP standards. The role requires reading SOPs, data entry, and collaboration with the manufacturing team. Training, lean participation,...
- ...a Senior Training and Development Associate responsible for designing, developing, and implementing training programs that support cGMP compliance and company policies. You will partner with Quality Assurance, Manufacturing, and other leaders to ensure training content...
- Johnson & Johnson is seeking a cGMP Compliance and Investigations Lead in Spring House, PA to champion deviation investigations, CAPA development, and risk-based remediation across cell therapy development and manufacturing. The role requires regulatory knowledge (FDA/...
- ...and warehousing lines. You will coordinate with QA, Supply Chain, and R&D to transfer new products to manufacturing and ensure strict cGMP compliance. The role emphasizes equipment upgrades, system validation, and strong analytical problem-solving to minimize downtime...
- ...Medicine, Department of Medicine, seeks a QC Specialist to oversee quality control testing for cell and gene therapy products in a cGMP facility. You will design and implement QC testing, review batch records, and support technology transfer from pre-clinical to cGMP....
$87.58k - $92k
...biologics and drugs for cell and gene therapy of internal/external users in the university's current Good Manufacturing Practices (cGMP) facility. The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and implementing quality control...Fixed term contractWork experience placementLocal area- Stokes Healthcare in Mount Laurel, NJ seeks a Chemistry Laboratory Assistant to support cGMP analytical chemistry operations, focusing on routine cleaning, sample receipt and distribution, and ordering laboratory supplies. Responsibilities include maintaining glassware...
- SGS Consulting in Vacaville, CA, seeks a Quality professional to support PQS integration and management of Quality Documents within Veeva. This on-site role requires 1-3 years of Quality experience in pharma or biopharma, preferably in supplier quality. Knowledge of Veeva...
- Hims & Hers in New Albany, OH is seeking a Compounding Operations Documentation Specialist to draft, revise, and maintain manufacturing documentation, including SOPs, work instructions, logs, forms, and compounding protocols, in support of regulated production. You will...
