QA Reviewer

Overview

Review and approve quality documents ensuring GMP compliance.

Key Responsibilities

• batch review
• report review
• document approval
• gmp compliance

Tasks

-Conduct thorough batch record reviews. -Evaluate and authorize Global Technical Reports (GTRs), Engineering Drawings, and Maintenance Work Requests/Work orders. -Review and approve Quality documents such as SOPs, Change Controls, and Validation protocols. -Ensure compliance with GMP regulations and quality assurance standards.

Requirements

• aseptic
• gmp
• bachelor's
• quality assurance
• pharma manufacturing
• batch records

What You Bring

-Familiarity with aseptic manufacturing and auditing processes. -Proficiency in GMP regulations. -Bachelor's degree in Science. -Experience in quality assurance and documentation review. -Experience in a scientific discipline, preferably in pharmaceutical manufacturing. -Strong understanding of batch record processes.

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Benefits

-Employee Assistance Program -Short and long-term disability -Time Off/Leave (PTO, Vacation or Sick Leave) -Medical, dental & vision -Life Insurance (Voluntary Life & AD&D for the employee and dependents) -Critical Illness, Accident, and Hospital -Health Spending Account (HSA) -Transportation benefits -401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available

About Actalent

-Born in July 2021 by merging Aerotek’s engineering & sciences arm with EASi, Actalent emerged as a focused engineering-and-science partner. -Backed by Allegis Group, it drives scale and speed to market via contract, managed, and technical services. -Headquartered in Maryland with global reach, it deploys specialized teams across North America, Europe, and APAC on Fortune 500 projects. -Typical engagements span EV design, vaccine development, lab services, clinical research, and infrastructure systems. -Expertise covers a wide spectrum: aerospace, defense, healthcare, manufacturing, software systems, environmental and civil engineering.

Sector Specialisms