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Warehouse Supervisor About Site The newly launched manufacturing facility on Adair Blvd marks a pivotal expansion of Catalent’s Zydis® technology, a globally renowned, fast-dissolve oral dosage form that has…
Account Executive – Late Phase Position Summary: Catalent Pharma Solutions is recruiting for an Account Executive, Rx Pharmaceutical Softgel and Late-Stage Oral Solids. This position will be field-based and will be…
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…
The Technical Writer collaborates with subject matter experts to create and maintain manufacturing documentation, such as Master Batch Records, ensuring compliance with Good Manufacturing Practice (GMP) standards. This onsite role involves managing document databases, supporting regulatory audits, and coordinating cross-functional project documentation.
Senior Process Engineer - Equipment 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…
Leads pharmaceutical/biotech projects from initiation to completion, ensuring timelines, client satisfaction, and quality delivery in a cGMP clinical manufacturing environment.
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 a Finance…
Oversees clinical trial quality assurance, ensuring compliance with regulations, GMPs, and SOPs while validating testing methods, calibrating equipment, and managing deviations.
Ensures compliance with regulatory requirements and GMP standards in clinical trial projects, maintaining documentation and supporting quality processes for drug delivery products.
The Project Manager oversees non-technical aspects of inhalation drug development and manufacturing projects, serving as the primary point of contact for customers. They manage project lifecycles, timelines, and budgets using standard project management tools and methodologies.
Project Coordinator managing non-technical aspects of inhalation product development and manufacturing projects at Catalent's Chelsea, MA site, using Adobe Workfront and Microsoft Office to coordinate project lifecycles, track tasks, and facilitate client communication.
Manager, Quality Assurance leading QA associates at Catalent's Kansas City drug delivery facility — reviewing/approving batch documentation, deviations, investigations, change control, and IQ/OQ/PQ validations while ensuring GMP compliance.
Process Engineer - Engineering About Site Catalent’s Madison, Wisconsin site is a state‑of‑the‑art biologics development and manufacturing facility supporting customers from research through early‑ and mid‑stage…
Project Engineer 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 located 5 miles…
Warehouse Lead Catalent’s Malvern, Pennsylvania site—known as Catalent Micron Technologies—specializes in particle size reduction and advanced materials science services that support drug development from early stages…
Laboratory Analyst About Site Catalent’s Greenville, North Carolina site is a major oral solid dose development and manufacturing campus, delivering end‑to‑end, turnkey solutions from formulation development through…
Computer System Engineer 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…
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.
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