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American pharmaceutical company
Perform real-time quality checks on pharmaceutical manufacturing, reviewing documents, testing samples, and ensuring cGMP compliance for oral solid dose products.
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.
On-site QA role ensuring GMP compliance for biologic drug manufacturing in Madison, WI. Daily tasks include batch record review, document control, and auditing to safeguard product quality and regulatory adherence.
Oversee pharmaceutical manufacturing projects, from equipment installation to regulatory approval, ensuring compliance with cGMP standards and delivering on time and budget.
QC Chemist I 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 manufacturing for oral and…
Manager, Manufacturing, Fill Finish Position Summary: Work Schedule: Monday – Friday, 8am-5pm 100% on-site Catalent is a leading global CDMO, partnering with pharmaceutical, biotech, and self-care companies to…
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.
About Site Our Bridgewater location is the corporate office for Catalent. The facility is located approximately 45 minutes from Newark Liberty airport. Position Summary Catalent is a global leader in clinical supply…
Senior Account Director , Cell & Gene Therapy Position Summary Catalent is seeking a Senior Account Director, Cell & Gene Therapy to drive new business acquisitions across our Cell & Gene Therapy…
Process Engineer MS&T About Site Catalent’s Princeton, New Jersey site is a key part of the company’s cell therapy network and serves as a U.S. commercial manufacturing facility for autologous and allogeneic cell…
About Site Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. Position Summary We have an opportunity for an…
Manager, Biochemical Analysis Role About Site Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. Position Summary…
Process Engineer About Site Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. Position Summary We have an…
En Catalent estamos buscando un Operario de Encapsulado para nuestra planta productiva de Buenos Aires. Principales Responsabilidades: Preparar las máquinas de encapsulado y elaborar capsulas de gelatina a partir de la…
Quality Control Technician I About Site Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. Position Summary We have…
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…
Develop and test early-stage drug formulations in a pharma lab, following protocols to prepare preclinical and clinical products under supervision.
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