QA Specialist

Our client, a leader in pharmaceutical manufacturing and quality assurance, is seeking a QA Specialist to join their team. As a QA Specialist, you will be part of the Quality Assurance department supporting the clinical trial manufacturing and packaging processes. The ideal candidate will have meticulous attention to detail, strong communication skills, and a proactive approach to problem-solving, which will align successfully in the organization.

Job Title: QA Specialist
Location: Zebulon, NC
Pay Range: $45
Duration: 12 months

What's the Job?

• Serve as a Batch Release Officer for the review and recommended release of documentation for a range of dosage form batches and finished clinical trial packs of Investigational Medicinal Products in accordance with GMP requirements.
• Assess Quality QMS Records such as Deviations and complaints, make recommendations for corrective and preventative actions, and follow up on their implementation.
• Review and approve GMP documentation, including Standard Operating Procedures, Change Controls, and other controlled documents from business partner areas.
• Provide advice and support to business partner areas relating to quality matters and process improvements.
• Participate in audits, assessments, regulatory inspections, and high-priority projects, including addressing non-compliance issues.

What's Needed?

• Bachelor's degree or equivalent work experience with 5+ years in a similar role.
• Experience reviewing GMP manufacturing, packaging documentation, or laboratory records of pharmaceutical dosage forms.
• Knowledge of GMP principles and decision-making based on GMP standards.
• Experience leading or participating in QMS activities such as Deviations, Complaints, Change Controls, and audits.
• Proficient in Microsoft Windows applications (Word, Excel, PowerPoint).

What's in it for me?

• Opportunity to work in a dynamic and impactful environment dedicated to quality and compliance.
• Engagement in meaningful projects that support global health initiatives.
• Collaborative team culture that values innovation and continuous improvement.
• Professional growth through exposure to regulatory inspections and high-priority initiatives.
• Competitive pay rate aligned with industry standards.

Upon completion of waiting period consultants are eligible for:

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• Health Savings Account
• Health Flexible Spending Account
• Dependent Care Flexible Spending Account
• Supplemental Life Insurance
• Short Term and Long Term Disability Insurance
• Business Travel Insurance
• 401(k), Plus Match
• Weekly Pay

If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!

About ManpowerGroup, Parent Company of: Manpower, Experis and Talent Solutions.

Experis® is a global leader in technology services and part of the ManpowerGroup® (NYSE: MAN) family of brands. We connect skilled technology professionals with meaningful opportunities where they can grow their careers, expand their expertise and make a real impact. Guided by the belief that it takes Human Ingenuity to unlock the true potential of technology, Experis helps people gain experience with leading organizations, build sought-after skills and take the next step toward a brighter future. Backed by ManpowerGroup's 75+ years of workforce expertise and global reach across more than 70 countries and territories, Experis brings the scale, insight and opportunity to help people and businesses thrive. ManpowerGroup is consistently recognized for its commitment to inclusion, ethics and responsible business, including being named one of the World's Most Ethical Companies. Learn more at Experis.com.