Pharma Quality Control Specialist in Ohio (Long-Term)

Stark Pharma Solutions Inc; Dublin (OH); On-site; USD 60,000 - 90,000; Full time

Job summary

Stark Pharma Solutions Inc. in Ohio is seeking a Quality Control Specialist with experience in pharmaceutical manufacturing and lab environments to support testing, documentation, and quality control activities in a regulated setting.

Responsibilities include performing QC testing, reviewing results, maintaining records, and ensuring GMP/SOP compliance while collaborating with QA, Manufacturing and Lab teams to drive quality improvements.

Qualifications

• Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or related field.
• 3+ years in Quality Control in pharma/regulated industries.
• Experience with pharmaceutical lab testing and documentation.
• Knowledge of GMP and laboratory SOPs.
• Experience with OOS/OOT investigations and quality documentation.
• Strong analytical, documentation, communication, and problem-solving skills.
• Ability to work with cross-functional teams.

Responsibilities

• Perform routine QC 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.
• Support investigations of OOS and OOT results.
• Maintain laboratory equipment and ensure proper calibration and operation.
• Work with QA, Manufacturing, and Laboratory teams to resolve quality issues.
• Support audits, inspections, and continuous improvement activities.

Skills

Analytical skills

Documentation

Communication

Problem-solving

Cross-functional teamwork

Education

Bachelor's degree in Chemistry/Biology/Pharmaceutical Sciences

Job description

Stark Pharma Solutions Inc. in Ohio is seeking a Quality Control Specialist with experience in pharmaceutical manufacturing and lab environments to support testing, documentation, and quality control activities in a regulated setting.

Responsibilities include performing QC testing, reviewing results, maintaining records, and ensuring GMP/SOP compliance while collaborating with QA, Manufacturing and Lab teams to drive quality improvements.