Job Description
We are seeking a Quality Assurance Associate to support a major pharmaceutical client. The QA Associate will be responsible for real-time batch record review on the manufacturing shop floor, among other duties.
ResponsibilitiesExecute real-time review of batch documentation and other manufacturing documentation, analyzing for errors, corrections, and compliance.Perform housekeeping and GMP walkthroughs of the facility.Initiate and participate in triage for on-the-floor events.Collaborate with cross-functional teams to meet and exceed timelines.Execute or review room and line clearances.Make quality decisions in real-time according to regulations ICH Q7 and 21CFR211 and internal procedures.Essential SkillsBatch Record Review experience.GMP experience in a manufacturing facility.At least 6 months of pharmaceutical quality experience.Additional Skills & QualificationsExperience with quality assurance in the pharmaceutical industry.Knowledge of vaccine manufacturing processes.Work Environment
The role involves working on the shop floor 90-100% of the shift. The work environment includes both pharma manufacturing areas and office space with a desk. The position requires adherence to aseptic gowning procedures and has a dress code of business casual with closed-toed shoes.
Pay and BenefitsThe pay range for this position is $35.00 - $40.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Sanford,NC.
Application Deadline
This position is anticipated to close on Aug 8, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.