Catalent

Open 30d On-siteNorth America

Specialist I, Quality Assurance

About Site Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. Position Summar y We have an opportunity for a…

Open 33d On-siteNorth America

Quality Assurance Associate

Canada

About Site Strathroy, Ontario is one of two sites located in Canada offering softgel development and manufacturing capabilities for the Pharmaceutical and Consumer Health industries. We have a broad range of integrated…

Open 35d On-siteNorth AmericaSenior

Senior Specialist, Quality Assurance III

Senior Specialist, Quality Assurance III About Site Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. Position…

Six Sigma

Open 40d On-siteNorth America

Quality Assurance Auditor - Analytical Review

Job Description 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 commercial…

Open 40d On-siteNorth America

Supervisor - Quality Assurance

Corrective Action Risk Assessment Root Cause Analysis

Supervisor - Quality Assurance Position Summary: Shift: M-F 8am-5pm Location: Madison, WI 100% Onsite Catalent’s Madison, Wisconsin site is a state‑of‑the‑art biologics development and manufacturing facility supporting…

Open 47d On-siteNorth AmericaInternship

QA Analytical Auditor

QA Analytical Auditor About Site Catalent’s Winchester, KY site is the company’s flagship U.S. manufacturing location for large‑scale oral solid dose forms, operating from a 180,000‑square‑foot facility with fully…

Open 47d On-siteNorth America

Specialist, QA Validation & Engineering

Specialist, QA Validation & Engineering 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…

Risk Assessment

Open 51d On-siteNorth America

Quality Assurance Associate

Canada

Quality Assurance Associate About Site The newly launched manufacturing facility on Adair Blvd marks a pivotal expansion of Catalent’s Zydis® technology, a globally renowned, fast-dissolve oral dosage form that has…

Open 55d On-siteNorth America

Specialist III – Quality Assurance, Systems

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.

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 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

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 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

Open 68d On-siteNorth America

Quality Assurance Associate

Corrective Action Root Cause Analysis Six Sigma Technical Writing

Perform real-time quality checks on pharmaceutical manufacturing, reviewing documents, testing samples, and ensuring cGMP compliance for oral solid dose products.

Open 68d On-siteNorth America

Quality Assurance Supervisor

Canada

Supervise a QA team in a pharmaceutical manufacturing plant, ensuring cGMP compliance, batch release, and quality systems while resolving deviations and training staff.

Open 69d On-siteNorth AmericaSenior

Senior Associate I - Quality Assurance Operations, On the Floor

On-site QA role ensuring GMP compliance for biologic drug manufacturing in Madison, WI. Daily tasks include batch record review, document control, and auditing to safeguard product quality and regulatory adherence.

Regulatory Compliance

Open 77d On-siteNorth AmericaSenior

3 months ago

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 86d On-siteNorth America

3 months ago

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

3 months ago

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