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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.
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…
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…
Review and approve batch records for clinical drug packaging to ensure GMP compliance and timely release, serving as the liaison between Catalent and client quality teams.
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…
Review and approve pharmaceutical quality-control data to ensure regulatory compliance and patient safety in a biologics manufacturing environment.
On-site QA specialist ensuring cGMP compliance for biologic drug manufacturing, reviewing documents, investigating deviations, and managing cell bank inventory at a Madison facility.
Oversee incoming material inspection, specifications, and lifecycle records for biologics manufacturing to ensure FDA compliance and support drug production for patient treatments.
Manages document control systems and ensures compliance with FDA and internal quality standards for a biologics manufacturer producing therapies for COVID-19, cancer, and other diseases.
Responsable développement produit Location: Beinheim, France Time Type: Full time Job Description Pour notre site de développement et de production implanté à Beinheim, à 30min de Strasbourg (67), nous recherchons pour…
Oversee quality assurance for biopharmaceutical manufacturing, validating equipment and processes to ensure GMP compliance and support production of life-saving therapies.
Validation Engineer Location: Chelsea, MA Time Type: Full time Job Description Validation Engineer Position Summary: Work Schedule: Monday - Friday, 8:00am to 5:00pm 100% on-site The Chelsea facility is Catalent’s…
Engineer, Facilties Location: Harmans, MD Time Type: Full time Job Description Engineer, Facilities About Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the…
Oversee clinical supply packaging projects for global drug trials, manage a team, and ensure on-time delivery while maintaining regulatory compliance.
Über den Standort Catalent Schorndorf ist ein zentraler Bestandteil des europäischen und globalen Netzwerks für klinische Versorgung von Catalent und bietet umfassende Dienstleistungen im Bereich der klinischen…
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…
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