1st Shift Quality Control Laboratory Technician

Overview

The GMP Associate Scientist is responsible for the complete testing and results documentation of finished goods, stability and in-process samples within the QC Chemistry/Micro Laboratory, in a manner consistent with established standards. This individual must have prior GMP experience.

• Up to 50% environmental monitoring, water testing, Preparatory Set Up
• Perform calibrations/standardizations of instruments such as balances and pH meters
• assist with lab inventory such as stocking, receiving and storing media/solutions as necessary
• Prepare and stage the solution for testing by senior analysts
• Understand and follow the Data integrity Up to 20% Testing/Documentation/Data Review
• Independently perform core techniques or methods as assigned for testing on raw materials, finished goods, stability and in-process samples.
• Perform testing that has the highest level of difficulty compared to other testing methods.
• Ensure that the calibration of critical laboratory equipment is current before use.

• Clean and organize all laboratory areas including bench, sinks, drawers, cabinets, solvent cabinets, fume hoods, refrigerators, freezers, desiccators and storage areas.
• Occasionally clean laboratory pipettes and other glassware.
• Maintain laboratory instruments disposing of wastes, cleaning them and replacing consumable parts as required.
• Ensure the lab areas are audit ready at all times

• Participate in ongoing training for the development of skills and responsibility with an emphasis on technology.
• Perform training of other analysts in areas of expertise, such as but not limited to chromatographic techniques, laboratory documentation, and documentation review.
• Ability to actively participate on various and/or lead laboratory projects or teams and propose solutions to problems encountered by such teams.

Skills
Gmp, Biology, Quality control, Cleanroom, Pharmaceutical, Wet chemistry, analytical chemistry, chemistry, Aseptic technique, Laboratory, Sop, Cgmp, Sterilization, raw material testing, Quality assurance

Top Skills Details
Gmp,Biology,Quality control,Cleanroom,Pharmaceutical,Wet chemistry,analytical chemistry,chemistry

• Bachelor’s degree in chemistry, Microbiology, Biology, Biochemistry or related field, Experience in a Quality Control Laboratory in GMP Pharmaceutical facility preferred.

This is a Contract position based out of High Point, NC.

The pay range for this position is $23.00 - $23.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• 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)

Workplace Type This is a fully onsite position in High Point, NC.

Final date to receive applications This position is anticipated to close on Jan 23, 2026.

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

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 due to a disability, please email actalentaccom for other accommodation options.