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American pharmaceutical company
Manager - Commercial Operations Position Summary : Catalent is seeking a Manager - Commercial Operations to support our Madison, Wisconsin Cell Line Development business. This role serves as the commercial lead for…
Marketing Specialist Location: Bridgewater, NJ or in Philadelphia, PA preferred with minimal travel Position Summary: The Marketing Specialist supports the execution of integrated marketing programs for Catalent’s…
Associate Director of Engineering, Facilities 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…
Product Manager coordinating Catalent's Quality Assurance operations at the Winchester, KY pharmaceutical manufacturing site, serving as the primary quality liaison for clients and handling audits, investigations, complaints, and quality agreements using Microsoft Office and Trackwise/JDE.
Oversees quality systems and compliance for biopharmaceutical manufacturing, managing deviations, CAPAs, and investigations while collaborating with stakeholders to ensure operational excellence in a GMP facility.
Supervisor - Quality Control Position Summary: Work Schedule: M-F 8am-5pm 100% on-site Catalent’s Madison, Wisconsin site is a state‑of‑the‑art biologics development and manufacturing facility supporting customers from…
Buyer/Planner II - Supply Chain 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…
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 Quality…
Pharmaceutical Development Senior Associate Scientist I Position Summary: Work Schedule: 2nd shift Monday – Thursday, 12pm-10pm 100% on-site Catalent’s Kansas City (KCM) facility is a premier site for integrated drug…
Process Engineer - Manufacturing Sciences & Technology (MS&T), Downstream Technology Transfer Position Summary: Work Schedule: Monday – Friday, core hours 8am-5pm 100% on-site (Madison, WI) On-call rotation…
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…
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.
Packaging Technician 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…
Associate Scientist II - Quality Control Position Summary: Work Schedule: M-F 8am-5pm 100% on-site Catalent’s Madison, Wisconsin site is a state‑of‑the‑art biologics development and manufacturing facility supporting…
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.
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