Actalent
Environmental Monitoring Technician
Actalent, High Point, North Carolina, United States, 27260
Associate Scientist
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? Understand and follow the data integrity 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.
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? Understand and follow the data integrity 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.