Catalent

Reliability Engineering Manager

Open 31d On-siteCIS

Six Sigma Technical Writing

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…

Open 31d On-siteCISSenior

Senior Specialist QA OTF Support

Open 30d On-siteNorth America

On-site QA specialist ensuring GMP compliance for gene therapy manufacturing by reviewing batch docs, inspecting drug product, and resolving deviations in real time.

Quality Assurance Associate

Canada

Review manufacturing documentation for compliance, coach staff on cGMP practices, and verify line clearances in a pharmaceutical softgel production facility.

48K – 57K CAD

Open 30d On-siteNorth AmericaSenior

Sr. Manager, Project Management

Sr. Manager, Project Management Position Summary: Shift: M-F 8am-5pm Location: Philadelphia, PA 100% Onsite Catalent’s Philadelphia, Pennsylvania site serves as the company’s North American Center of Excellence for…

Regulatory Compliance

Open 31d On-siteNorth AmericaSenior

Senior Quality Assurance Releaser

Reviews pharmaceutical batch records for compliance, approves documentation, and releases products to ensure cGMP standards and customer specs are met.

Open 32d On-siteNorth AmericaPrincipal

Principal Process Engineer - Manufacturing Sciences & Technology, Upstream

Gap Analysis Process Improvement Regulatory Compliance

Principal Process Engineer leads tech transfer, process improvements, and GMP manufacturing support for mammalian cell culture biologic production in a 100% onsite Madison facility.

Project Coordinator (m/w/d) - befristet auf 2 Jahre

Open 34d Europe

Germany

Coordinate pharmaceutical manufacturing projects, track timelines, and liaise with clients using tools like JDE and Fusion Suite.

Business Development CSS

Open 34d RemoteUKContract

Business Development Director

United Kingdom

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…

Business Development

Open 38d On-siteNorth America

Validation Process Engineer

Engineer who validates pharmaceutical manufacturing equipment and processes to meet regulatory standards, authoring protocols and managing projects from installation through performance verification.

Six Sigma

Open 37d On-siteNorth AmericaSenior

Senior Scientist, Analytical Development, Manager

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…

Open 39d On-siteCISSenior

Senior Director, Quality

Senior Director of Quality Position Summary: 100% on-site in Harmans, MD Catalent’s Baltimore facility is a leading center for biologics development and manufacturing, offering state-of-the-art capabilities in clinical…

Open 39d On-siteNorth AmericaContract

Manager, Facilities

Regulatory Compliance Vendor Management

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…

Open 80d On-siteCISContractSenior

Senior Program Manager

Analytics Program Management

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,…

119K – 163K $

Open 67d On-siteNorth AmericaContract

Specialist II Environmental Biochemist – Environmental, Health, Safety & Security

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.

Senior Project Manager Demand and Supply Planning (m/w/d)

Open 65d EuropeSenior

Germany

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.

VBA

Open 40d On-siteNorth America

Project Coordinator

Coordinates clinical-supply projects for a global pharma-services firm, tracking timelines, milestones, and documentation to ensure on-time, compliant delivery for patient trials.

Manager, Process Excellence

Open 40d On-siteUK

United Kingdom

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…

CSS Six Sigma

Open 40d On-siteNorth America

Manager Quality Assurance Operations

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.

Regulatory Compliance

130K – 160K $

Open 79d On-siteNorth AmericaContract

Supervisor, Quality Assurance