Quality Assurance Specialist Position Available In Wilson, Tennessee

Job Description:

Primary Talent Partners has a 12-month contract opening for aQuality Assurance Specialist to join a multinational pharmaceuticalcompany for an onsite position operating out of Wilson, NC. While professional experience and qualifications are key for thisrole, make sure to check you have the preferable soft skills beforeapplying if required.

Pay:

$40/hr – $45/hr

Contract:

12 months, extensions likely, conversion possible

Type:

W-2, cannot support C2C or provide visa sponsorship

Location:

Wilson, NC Job Description:

The Specialist, Quality Assurance supports key functions includingbatch record management, documentation generation (Certificates ofCompliance and Analysis), review of batch records for domesticrelease, and oversight of finished product conformance. This roleensures compliance with regulatory standards by supportinginvestigations, audits, SOP development, and supplier qualityinitiatives. The QA Specialist must demonstrate leadership,critical thinking, and the ability to work independently whilealigning with production timelines and site complianceexpectations.

Responsibilities:

Retrieve and track site batch records, includingarchiving, scanning, and filing. Manage document retention logistics, including offsite storage anddestruction past retention periods. Maintain accurate allocation and organization of Document RetentionRoom capacity. Assist in reconciling high/medium controlled print documents. Prepare and provide Certificates of Compliance (CoC) and supportCertificate of Analysis (CoA) generation. Track and process Registered Country Table (RCT) tender requestsand SAP allocations for global markets. Review batch records and support release of intermediate/finishedproducts for domestic distribution. Provide QA review and approval of GMP-related SOPs and supportcontinuous improvement of procedures. Participate in defect resolution and ensure control of materialsthroughout the plant. Lead and support quality investigations, including root causeanalysis and corrective action implementation. Contribute to Quality Master Data builds, maintenance, and PCRstrategy meetings. Support implementation of new regulatory programs and divisionalinitiatives. Identify and execute continuous improvement opportunities incollaboration with cross-functional teams. Maintain 5S compliance and promote workplace safety and incidentprevention.

Education:

Bachelor’s degree (B.A./B.S.) required, preferably inScience or Engineering.

Skills/Experience Required:

Minimum of 3 years’ experience in aGMP-regulated pharmaceutical manufacturing environment. Direct or indirect Quality Assurance experience, including batchrecord reviews, investigations, complaints, or compliancesupport. Strong communication and teamwork skills, both written andverbal. Highly detail-oriented with strong problem-solving and timemanagement abilities. Experience with information systems such as SAP and Veeva Systems;capable of generating reports and analyzing data. Able to independently manage data requests and trend analysis forprocess improvement. Adaptable and able to multitask under pressure while meetingproject deadlines. Nice to

Haves:

Experience supporting audits, regulatoryinspections, and supplier quality programs. Familiarity with 5S methodologies and Lean/Continuous Improvementpractices. Primary Talent Partners is an Equal Opportunity / AffirmativeAction employer committed to diversity in the workplace. Allqualified applicants will receive consideration for employmentwithout regard to race, color, religion, sex, sexual orientation,age, national origin, disability, protected veteran status, genderidentity, or any other factor protected by applicable federal,state, or local laws. If you are a person with a disability needing assistance with theapplication or at any point in the hiring process, please contactus at info@primarytalentpartners.com #PTPJobs #LI-PTP