QC Scientist II; Bioassay

Job Title

QC Scientist II (Bioassay)

In this role, you will utilize a variety of analytical tools for large molecule analysis, including Compendial Testing (pH, UV, Osmolality, and more), supporting GMP manufacturing for commercial product testing alongside Stability testing. Experience in a cGMP environment is essential.

• Perform ELISA, Compendial Testing, Enzyme Activity Assays, and other minor equipment testing on In-Process, DS release, and stability samples, ensuring timely delivery for projects.
• Review laboratory data packets as assigned.
• Perform and author laboratory investigations as assigned.
• Conduct GMP testing in an analytical laboratory environment using HPLC and UPLC test methods.
• Compile data for documentation of test procedures and prepare reports.
• Collaborate with team members and other departments such as quality assurance and data reviewers.
• Contribute to the development of new concepts, techniques, and standards.
• Recognize and report invalid, lab incident, out-of-specification, and out-of-trend results to laboratory management and recommend solutions.
• Perform all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, and safety guidelines.
• Participate in laboratory activities, perform safety inspections, and order supplies.

• Experience in GMP regulated environment, preferably pharmaceuticals.
• Experience with compendial methods (pH, Osmolality, UV).
• Proficiency in ELISA, Compendial Testing, Enzyme Activity Assays, Spectrometer, Plate Readers.
• Qualitative pipetting skills.

• Bachelor’s degree in chemical pharmaceutical, biology, chemistry, biotechnology or related field.
• 1-4 years of proven experience in a GMP regulated environment.
• Knowledge of SoloVPE, qPCR, Color metric-based assays, and multi-channel pipetting.
• Familiarity with EMPOWER, MS Office, and laboratory computer programs.
• Flexibility, good organization and planning skills, attention to details, positive and collaborative demeanor.

This is a newly formed team of 7 within the QC Analytical team, comprising over 80 members. The role involves working in a pharmaceutical lab setting, doing bench work. Training will last 3-6 months, requiring testing on each test before moving forward. The position operates Monday-Friday with flexible start times (8am-4pm) and involves a stat or test every 6 weeks in the evening or on the weekend, lasting 2-3 hours.

This is a Contract to Hire position based out of Berkeley, MO.

The pay range for this position is $30.00 - $38.46/hr.

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Anticipated to close on Jun 25, 2026.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccom for other accommodation options.