Quality Control Scientist I

TekWissen ®; Cincinnati (OH); On-site; USD 28,000 - 39,000; Full time

Job summary

TekWissen® Group is seeking a detail-oriented Quality Control Scientist I to support pharmaceutical finished product testing and stability assessments. The role requires hands-on HPLC experience, routine data documentation, and adherence to cGMP/GLP standards in a fast-paced lab environment.

Responsibilities include routine chemical testing, instrument operation, sample preparation, and reporting out-of-spec results.

Qualifications

• Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related physical science.
• Hands-on experience with HPLC instrumentation.
• Knowledge of cGMP, GLP, SOPs, and regulatory standards.
• Ability to document analytical results accurately and maintain compliance.

Responsibilities

• Perform routine chemical testing of pharmaceutical finished products and stability samples using established analytical methods.
• Conduct analytical testing for product strength, impurities, identity, and other quality characteristics using HPLC, dissolution, and wet chemistry techniques.
• Operate analytical laboratory instrumentation and perform routine calibrations and verifications.
• Prepare mobile phases, diluents, reagents, and other laboratory solutions.
• Identify, document, and report out-of-specification (OOS) results and unexpected analytical findings.
• Maintain accurate laboratory records, test results, and supporting documentation.
• Follow SOPs, cGMP, and GLP; maintain equipment and work areas to safety and quality standards.
• Support QC laboratory activities and manufacturing operations.
• Troubleshoot routine analytical issues and communicate findings clearly.

Skills

Analytical chemistry

Troubleshooting

Detail oriented

Documentation

Education

Bachelor's degree in Chemistry or related field

Tools

HPLC instrumentation

GC techniques

Wet chemistry

Job description

Shift: Monday To Friday - First Shift - Should start the shift between 06:00 AM to 09:00 AM

Pay Rate: $20 to $28 depending on experience

Overview:

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to clients worldwide. The job opportunity below is with one of our clients specializing in biotechnology product development services. The client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As a global leader in serving the scientific community, the organization generates approximately $40 billion in annual revenue and is committed to making the world healthier, cleaner, and safer. Their global team delivers innovative technologies, convenient procurement solutions, and pharmaceutical services through industry-leading brands.

Summary

We are seeking a detail-oriented Quality Control Scientist I. The ideal candidate will have hands‑on experience with High‑Performance Liquid Chromatography (HPLC), chemical testing, and analytical laboratory techniques. This position involves testing pharmaceutical finished products and stability samples, performing routine analytical procedures, and ensuring compliance with established quality and regulatory standards.

Responsibilities

• Perform routine chemical testing of pharmaceutical finished products and stability samples using established analytical methods.
• Conduct analytical testing for product strength, impurities, identity, and other quality characteristics using HPLC, dissolution, and wet chemistry techniques.
• Operate analytical laboratory instrumentation and perform routine calibrations and verifications.
• Prepare mobile phases, diluents, reagents, and other laboratory solutions.
• Identify, document, and report out‑of‑specification (OOS) results and unexpected analytical findings.
• Maintain accurate laboratory records, test results, and supporting documentation.
• Follow established Standard Operating Procedures (SOPs), Good Manufacturing Practices (cGMP), and Good Laboratory Practices (GLP).
• Maintain laboratory equipment and work areas in accordance with safety and quality standards.
• Support QC laboratory activities, testing schedules, and manufacturing operations.
• Troubleshoot routine analytical issues and communicate findings effectively.

Required Skills

• Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related physical science discipline.
• 1–2 years of experience in chemical or analytical laboratory testing using HPLC or GC techniques.
• Equivalent combinations of education, training, and relevant laboratory experience may be considered.
• Hands‑on experience and working knowledge of HPLC instrumentation are required.
• Knowledge of analytical chemistry, qualitative and quantitative testing, laboratory instrumentation, wet chemistry techniques, and sample preparation.
• Understanding of cGMP, GLP, SOPs, and pharmaceutical quality and regulatory standards.
• Ability to accurately document analytical results, follow established laboratory procedures, and maintain compliance with safety and quality guidelines.
• Strong analytical, troubleshooting, problem‑solving, and organizational skills with excellent attention to detail.
• Effective written and verbal communication skills, with the ability to multitask and work efficiently in a fast‑paced laboratory environment.
• Ability to stand, walk, bend, and perform laboratory activities for extended periods.
• Ability to lift and move materials weighing approximately 10–35 lbs.
• Ability to operate laboratory equipment safely and wear required personal protective equipment (PPE).

TekWissen® Group is an equal opportunity employer supporting workforce diversity.