Description
Job Description: Job Description:\t
The Associate Scientist – is responsible for the complete testing and results documentation of any finished goods, stability and in-process samples within the QC Chemistry/Micro Laboratory, in a manner consistent with established standards.
What will you do?
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.
Up to 25% Housekeeping
• 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
Up to 5% Training and Development
• 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
Microbiology, Environmental monitoring, Gmp, Biology, Quality control, Cleanroom, Pharmaceutical, Aseptic technique, Laboratory, Sop, Cgmp, Sterilization, raw material testing
Top Skills Details
Microbiology,Environmental monitoring,Gmp,Biology,Quality control,Cleanroom,Pharmaceutical
Additional Skills & Qualifications
Education & Experience
• Bachelor’s degree in chemistry, Microbiology, Biology, Biochemistry or related field, Experience in a Quality Control Laboratory in GMP Pharmaceutical facility preferred.
Experience Level
Intermediate Level
Pay and Benefits
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.
Application Deadline
This position is anticipated to close on Aug 28, 2025.
About Actalent
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 actalentaccommodation@actalentservices.com for other accommodation options.