Catalent

Open 72d On-siteNorth America

2 months ago

Process Engineer

Corrective Action Risk Assessment Six Sigma

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…

Open 75d On-siteNorth America

Quality Control Technician I

Quality Control Technician 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…

Confined Space

Open 75d On-siteNorth AmericaSenior

Senior Manager, Supply Chain

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…

Open 76d On-siteNorth America

Reliability Engineering Manager

Confined Space Personal Protective Equipment (PPE) Root Cause Analysis 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 75d On-siteNorth America

Supervisor, Manufacturing

Job Description Supervisor, Manufacturing 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…

Process Improvement

Open 77d On-siteNorth America

Associate Scientist, Product Development

Develop and test early-stage drug formulations in a pharma lab, following protocols to prepare preclinical and clinical products under supervision.

71K – 72K $

Open 77d On-siteNorth AmericaInternshipIntern

Lab Assistant (Intern), Analytical Development

Part-time internship assisting in a pharmaceutical lab, cleaning glassware, preparing reagents, and running routine analytical chemistry experiments under supervision.

20 – 20 $ / hr

Open 77d 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.

Corrective Action

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.

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

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