Job Description
Perform quality control testing in the QC Testing Laboratory according to approved SOPs and in compliance with cGMP regulations to ensure consistent production of products and support ongoing stability studies. Understand proper operation of all instrumentation and equipment within the laboratory and perform required maintenance, clean benchtops, hoods, and laboratories, and dispose of biohazardous waste. Organize and handle testing samples and maintain testing inventory. Assist with the maintenance of the equipment qualification and calibration program and upkeep of the equipment database. Assist the QA/QC Manager with review and filing of calibration certificates, out of tolerance reports, deviations, and SCARs as necessary. Assist with the development and implementation of company SOPs as assigned. Perform document control and training activities as assigned. Complete cGMP documentation accurately, in accordance with standard operating procedures, and in a timely manner. Work independently to accomplish given tasks within given timelines. Multitask and adjust to changing priorities. Report any deviations or nonconformities immediately to a Manager or Director. Perform other duties as assigned.
ResponsibilitiesPerform quality control testing in the QC Testing Laboratory according to approved SOPs and in compliance with cGMP regulations.Understand proper operation of all instrumentation and equipment within the laboratory.Perform required maintenance, clean benchtops, hoods, and laboratories, and dispose of biohazardous waste.Organize and handle testing samples and maintain testing inventory.Assist with the maintenance of the equipment qualification and calibration program.Upkeep the equipment database.Assist with the review and filing of calibration certificates, out of tolerance reports, deviations, and SCARs.Assist with the development and implementation of company SOPs.Perform document control and training activities.Complete cGMP documentation accurately and in a timely manner.Work independently to accomplish tasks within given timelines.Multitask and adjust to changing priorities.Report any deviations or nonconformities immediately to a Manager or Director.Perform other duties as assigned.Essential SkillsQuality control testingGMP complianceLaboratory instrumentation and equipment operationDocumentation skillsIndependent working abilityMultitasking and adaptabilityCommunication and organizational skillsAdditional Skills & QualificationsAssociate’s Degree in related field or equivalent work experience6 months to 1 or more years of previous related experiencePrior experience with 21 CFR 820 is a plusAbility to work efficiently under pressure and within deadlinesWork Environment
1st shift: Monday - Friday 8:00am - 4:30pm. Opportunity to grow from within. Breakfast provided every Friday. Potential for raise after the contract period (not guaranteed). Summer cookouts/ice cream socials. Small company feel but backed by a large corporation ensuring strong job security. Not micromanaged.
Pay and BenefitsThe pay range for this position is $20.00 - $22.00/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 Franklin,MA.
Application Deadline
This position is anticipated to close on Sep 5, 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.