Quality Control Specialist

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

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

Location:

Ohio

Duration:

Long Term

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.


• Support investigations of out-of-specification (OOS) and out-of-trend (OOT) results.


• 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.


• 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 effectively with cross-functional teams.

Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse backgrounds.