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American pharmaceutical company
Supervise a QA team in a pharmaceutical manufacturing plant, ensuring cGMP compliance, batch release, and quality systems while resolving deviations and training staff.
Oversee capital projects for a biologics manufacturing site, coordinating schedules, budgets, and cross-functional teams to deliver GMP-compliant facilities and equipment on time.
Oversee pharmaceutical manufacturing projects, from equipment installation to regulatory approval, ensuring compliance with cGMP standards and delivering on time and budget.
Ensure workplace safety and environmental compliance at a pharmaceutical manufacturing site by auditing processes, tracking hazards, and implementing EHS programs under OSHA, EPA, and ISO standards.
Senior Manager, Supply Chain Position Summary: Work Schedule: M-F 8am-5pm 100% on-site Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical…
Reliability Engineering Manager About Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities is…
Job Description Supervisor, Manufacturing About Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing…
Principal Process Engineer leads tech transfer, process improvements, and GMP manufacturing support for mammalian cell culture biologic production in a 100% onsite Madison facility.
Operate packaging machines for pharmaceutical products, inspect labels and components, and maintain compliance with cGMP and SOPs in a clinical/commercial production environment.
Senior Scientist, Analytical Development, Manager About Site Catalent’s San Diego, CA site is an early‑phase development facility supporting small‑molecule and peptide programs from preformulation through cGMP clinical…
Manager, Facilities Catalent’s Philadelphia, Pennsylvania site serves as the company’s North American Center of Excellence for clinical supply packaging, delivering comprehensive, end‑to‑end support for global clinical…
On-site role in Madison, WI ensuring OSHA/EPA compliance for a biomanufacturing CDMO, managing biochemical safety, hazardous waste, and EHS programs while embedding safety practices across operations.
Position Summary We have an opportunity for a Manager, Process Excellence to join our team and lead global process governance for clinical supply systems. In this role, you will ensure compliance, efficiency, and…
Oversees on-site Quality Assurance (QA) for cell therapy manufacturing, ensuring compliance with GMP regulations, batch record reviews, and real-time QA support in cleanroom environments.
Supervise a team ensuring pharmaceutical packaging and distribution meet strict quality and regulatory standards, using cGMP and SOPs in a manufacturing environment.
Oversee engineering, maintenance, and facilities at a gummy manufacturing site, ensuring compliance, reliability, and efficiency while leading capital projects and process improvements.
Oversee pharmaceutical quality systems and compliance at a new manufacturing site, ensuring cGMP standards and regulatory approvals for Catalent’s Zydis® drug technology.
Sr. Manager, Manufacturing Operations – Plasmids Position Summary: Work Schedule: Monday – Friday, 8am – 5pm. 100% on-site Catalent is a leading global CDMO partnering with pharma and biotech innovators to accelerate…
Manager, Quality and Compliance Position Summary: Work Schedule: M-F 8am-5pm 100% on-site Catalent Biologics is a fast-growing business within Catalent Pharma Solutions focused on providing innovative technologies and…
Technician I - Facilities, Maintenance Position Summary Shift: Tuesday - Friday 10:00pm - 8:00am 100% on-site $5,000 SIGN-ON BONUS OFFERED Catalent, Inc. is a leading global contract development and manufacturing…
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