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Job summary
Stark Pharma in Concord, NC is looking for a Quality Control (QC) Engineer / Analyst to support laboratory testing in a GMP-regulated environment. The role requires 2-6+ years of QC experience, strong analytical skills, and a Bachelor's degree in a relevant scientific field. Responsibilities include performing analytical tests, documenting results, supporting method validation, and ensuring compliance with regulatory standards. This is a long-term contract position focused on maintaining high-quality standards.
Qualifications
2-6+ years of experience in Quality Control within the pharmaceutical or biotech industry.
Hands-on experience with analytical techniques (e.g., HPLC, GC, UV).
Strong understanding of GMP and regulatory compliance.
Responsibilities
Perform analytical testing on raw materials, in-process samples, and finished products.
Document and review test results in compliance with GMP and regulatory requirements.
Support method validation, verification, and transfer activities.
Investigate out-of-specification (OOS) and out-of-trend (OOT) results.
Maintain laboratory equipment and ensure proper calibration and qualification.
Collaborate with Quality Assurance, Manufacturing, and Validation teams.
Ensure compliance with FDA, GMP, and company quality standards.
Skills
Analytical techniques (HPLC, GC, UV)
GMP compliance
Documentation practices
Data analysis
Education
Bachelor's degree in Chemistry, Biology, or related field
Job description
Stark Pharma in Concord, NC is looking for a Quality Control (QC) Engineer / Analyst to support laboratory testing in a GMP-regulated environment. The role requires 2-6+ years of QC experience, strong analytical skills, and a Bachelor's degree in a relevant scientific field. Responsibilities include performing analytical tests, documenting results, supporting method validation, and ensuring compliance with regulatory standards. This is a long-term contract position focused on maintaining high-quality standards.