Quality Specialist – Batch Records Position Available In Wilson, Tennessee
Tallo's Job Summary: We are hiring a Quality Specialist for batch records with a pay range of $40 - $45 an hour. Responsibilities include managing batch records, product release, SOP oversight, and regulatory compliance in pharmaceutical manufacturing. Qualifications require a Bachelor's degree in Science or Engineering, 3 years of GMP experience, proficiency in SAP and Veeva Systems, and strong communication and time management skills.
Job Description
Job Description:
About the
Role:
Apply below after reading through all the details and supportinginformation regarding this job opportunity. We are seeking a detail-oriented and proactive Quality AssuranceSpecialist to support key QA functions, including batch recordmanagement, product release, SOP oversight, and regulatorycompliance. This individual will play a critical role in ensuring GoodManufacturing Practices (GMP) and maintaining quality standards inpharmaceutical manufacturing.
Pay Range:
$40 – $45 an hr.
Key Responsibilities:
Perform batch record management tasks, including retrieval,archiving, scanning, and filing. Complete batch record reviews and support release of intermediateand finished products for domestic markets. Generate and provide Certificates of Compliance (CoC) andCertificates of Analysis (CoA) as needed. Support internal and external audits by compiling relevant data anddocumentation. Participate in investigations and quality issue resolutions. Review and develop Standard Operating Procedures (SOPs) incompliance with GMP. Provide Quality Assurance review and approval of GMP-relatedSOPs. Manage Supplier Quality and additional QA-related documentationprocesses. Oversee proper allocation and maintenance of the Document Retentionroom. Assist with reconciliation of controlled print documents. Track and process Registered Country Table (RCT) tender requestswithin SAP. Contribute to continuous improvement initiatives and ensureadherence to regulatory expectations.
Qualifications:
Education:
Bachelor’s degree (B.A./B.S.) in Science, Engineering, or a relatedfield.
Experience:
Minimum of 3 years of experience in a GMP-compliant pharmaceuticalmanufacturing facility. Hands-on experience in batch record reviews, documentation, productrelease, and quality systems.
Technical Skills:
Proficiency in SAP and Veeva Systems. Knowledge of QA tools and compliance standards.
Soft Skills:
Excellent communication (written and verbal) and teamworkabilities. Strong attention to detail and time management. Ability to manage multiple tasks under pressure and meet projectdeadlines. Skilled in identifying issues and implementing standard proceduresfor resolution. Capable of working independently and making informed decisionsusing data and trending analysis.
