Catalent

Open 78d On-siteNorth AmericaPrincipal

Principal Process Engineer - Manufacturing Sciences & Technology, Upstream

Gap Analysis Process Improvement Regulatory Compliance Risk Assessment

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

Open 83d On-siteNorth America

Pharmaceutical Packaging Technician II

Operate packaging machines for pharmaceutical products, inspect labels and components, and maintain compliance with cGMP and SOPs in a clinical/commercial production environment.

Open 82d 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 84d On-siteNorth America

Supervisor - Biomanufacturing, Upstream

Supervise upstream biomanufacturing operations in a GMP facility, ensuring quality, schedule, and cost targets while leading a team and maintaining regulatory compliance.

Regulatory Compliance

Open 85d 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 125d On-siteNorth AmericaContractSenior

Senior Program Manager

Analytics Microsoft Project 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 113d On-siteNorth AmericaContract

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

EPA Hazardous Waste Industrial Hygiene ISO 45001 OSHA +4 skills

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.

Open 86d 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 86d 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 86d 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 125d On-siteNorth AmericaContract

Supervisor, Quality Assurance

Supervise a team ensuring pharmaceutical packaging and distribution meet strict quality and regulatory standards, using cGMP and SOPs in a manufacturing environment.

Root Cause Analysis

Environmental Compliance OSHA Process Improvement Six Sigma

Director, Engineering

Open 119d On-siteAPAC

India

Oversee engineering, maintenance, and facilities at a gummy manufacturing site, ensuring compliance, reliability, and efficiency while leading capital projects and process improvements.

Open 119d On-siteNorth America

Director of Quality

Canada

Oversee pharmaceutical quality systems and compliance at a new manufacturing site, ensuring cGMP standards and regulatory approvals for Catalent’s Zydis® drug technology.

140K – 190K CAD

Open 89d On-siteNorth AmericaInternshipIntern

Lab Assistant (Intern), Quality Control

Part-time on-site internship in a pharmaceutical lab performing quality control tasks like cleaning glassware, preparing reagents, and assisting with experiments under supervision.

20 – 20 $ / hr

Open 89d On-siteNorth AmericaSenior

Sr. Manager, Manufacturing Operations - Plasmids

Sr. Manager, Manufacturing Operations – Plasmids Position Summary: Work Schedule: Monday – Friday, 8am – 5pm. 100% on-site Catalent is a leading global CDMO partnering with pharma and biotech innovators to accelerate…

Corrective Action

Likely evergreen On-siteNorth America

Manager, Quality and Compliance

Manager, Quality and Compliance Position Summary: Work Schedule: M-F 8am-5pm 100% on-site Catalent Biologics is a fast-growing business within Catalent Pharma Solutions focused on providing innovative technologies and…

Regulatory Compliance

Open 120d On-siteNorth AmericaContractSenior

Senior Program Manager - Program Management

Analytics PMP Program Management

Senior Program Manager - Program Management Position Summary: Work Schedule: M-F 8am-5pm 100% on-site Working for Catalent Biologics is an opportunity to join an entrepreneurial team. Catalent Biologics is making…

Open 90d On-siteNorth America

Environmental Health and Safety Manager

Confined Space Corrective Action Emergency Response Environmental Compliance EPA +7 skills

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…

Open 89d On-siteNorth America

Manager, Project Management

Manager, Project Management 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 Supply…