Catalent

Open 57d On-siteNorth America

Quality Assurance Specialist I

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…

Corrective Action

Open 58d On-siteNorth America

Technical Writer

Help Desk Technical Writing

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.

Open 62d On-siteNorth AmericaContractSenior

Senior Process Engineer - Equipment

Automation CMMS Confined Space Risk Assessment SCADA

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…

Open 62d On-siteNorth America

Project Manager

Microsoft Project Smartsheet

Leads pharmaceutical/biotech projects from initiation to completion, ensuring timelines, client satisfaction, and quality delivery in a cGMP clinical manufacturing environment.

92K – 102K $

Open 62d On-siteNorth America

Packaging Technician

Personal Protective Equipment (PPE) Regulatory Compliance

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…

Open 63d On-siteNorth America

Associate Scientist II - Quality Control

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…

Open 63d On-siteNorth AmericaSenior

Senior Specialist I, Quality Assurance

Oversees clinical trial quality assurance, ensuring compliance with regulations, GMPs, and SOPs while validating testing methods, calibrating equipment, and managing deviations.

Six Sigma

Business Development Networking Stakeholder Management

Account Director, Biologics, APAC

Open 63d APACContract

Singapore

Account Director, Biologics, APAC Position Summary Remote, Field-Based Location: Singapore or Japan Travel: Up to 60% across the APAC region Catalent is seeking an experienced and commercially driven Account Director,…

Open 63d On-siteNorth America

Specialist I, Quality Assurance

Ensures compliance with regulatory requirements and GMP standards in clinical trial projects, maintaining documentation and supporting quality processes for drug delivery products.

Open 63d On-siteNorth AmericaContract

Project Manager

Business Development Microsoft Project

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.

90K – 105K $

Open 63d On-siteNorth America

Manager, Quality Assurance

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.

Six Sigma

Process Engineer - Engineering

Automation Corrective Action Gap Analysis Risk Assessment Root Cause Analysis

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

Personal Protective Equipment (PPE) Six Sigma Technical Writing

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…

Regional Supervisor, GO, US

Regional Supervisor, GO, US Position Summary: Work Schedule: M-F 8am-5pm 100% on-site This position can sit at our Philadelphia, Kansas City, or San Diego site Catalent’s Kansas City facility is home to our Oral &…

Open 64d On-siteNorth AmericaJunior

Associate Scientist I - Quality Control, AQC (2nd shift)

Associate Scientist I - Quality Control, AQC Position Summary: Work Schedule: M-F 11am-7pm (2nd shift) 100% on-site Catalent Biologics is a fast-growing business within Catalent Pharma Solutions focused on providing…

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…

Open 65d On-siteNorth America

Laboratory Analyst

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…

API Process Improvement

Open 65d On-siteNorth America

Computer Systems Engineer I

Corrective Action Cybersecurity Networking Plc Regulatory Compliance

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…

Open 68d On-siteNorth AmericaInternshipIntern

Lab Assistant (Intern), Laboratory Operations

Lab Assistant (Intern), Laboratory Operations Position Summary: Work Schedule: Part-time (15-20/hours per week) Monday-Friday between 7 AM - 3:30 PM 100% on-site (San Diego) Catalent, Inc. is a leading global Contract…