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American pharmaceutical company
Our Swindon facility houses our Zydis® fast dissolving tablet development and manufacturing operation as well as a CMC pharmaceutical analytical lab services unit that offers ASAP stability. Position Summary We have an…
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…
Supervise upstream biomanufacturing operations in a GMP facility, ensuring quality, schedule, and cost targets while leading a team and maintaining regulatory compliance.
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…
Senior Program Manager Position Summary: Work Schedule: M-F 8am-5pm 100% on-site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus,…
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.
Leads demand and supply planning for a global CDMO, coordinating forecasts, S&OP processes, and cross-functional teams to align production with customer needs in pharma and biotech.
Coordinates clinical-supply projects for a global pharma-services firm, tracking timelines, milestones, and documentation to ensure on-time, compliant delivery for patient trials.
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.
Part-time on-site internship in a pharmaceutical lab performing quality control tasks like cleaning glassware, preparing reagents, and assisting with experiments under supervision.
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…
Senior Program Manager - Program Management Position Summary: Work Schedule: M-F 8am-5pm 100% on-site Working for Catalent Biologics is an opportunity to join an entrepreneurial team. Catalent Biologics is making…
Position Title: Director, Process Excellence Location: Philadelphia, PA Summary: The Director, Process Excellence serves as a key member of the Philadelphia Site Leadership Team and is responsible for driving…
About Site The ~70,000‑square‑foot Manassas facility operates within Catalent’s Consumer Health portfolio, supporting programs from early development through commercial manufacturing and packaging. It is designed for…
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