Quality Control Specialist

About The Company
Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success.

About The Company
Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success. Position: Quality Control Specialist Job Overview We are seeking a Quality Control Specialist with experience in pharmaceutical manufacturing and laboratory environments to support testing, documentation, and quality control activities in a regulated environment.

Key Responsibilities
Perform routine quality control testing of pharmaceutical products, raw materials, and samples. Review and document laboratory test results according to established procedures. Prepare and maintain QC records, reports, and documentation. Follow GMP, SOPs, and laboratory procedures during testing activities. Maintain laboratory equipment and ensure proper calibration and operation. Work with Quality Assurance, Manufacturing, and Laboratory teams to resolve quality issues. Support audits, inspections, and continuous improvement activities. Required Qualifications Bachelor s degree in Chemistry, Biology, Pharmaceutical Sciences, or a related field. 3+ years of experience in Quality Control within the pharmaceutical, biotech, or regulated industry. Experience with pharmaceutical laboratory testing and documentation. Experience with OOS/OOT investigations and quality documentation.