Description
\t\t\t\t\t•\tPerform quality control testing in the QC Testing Laboratory according to approved SOP’s and in compliance with cGMP and ISO 13485 regulations to ensure consistent production of products and support ongoing stability studies.•\tUnderstand proper operation of all instrumentation and equipment within the laboratory and perform required maintenance.•\tRecord Temperatures, clean benchtops, hoods, and laboratories and dispose of biohazardous waste.•\tOrganize and handle testing samples and maintain testing inventory.•\tAssist with the maintenance of the equipment qualification and calibration program and upkeep of the equipment database.•\tAssist the QA/QC Manager with review and filing of calibration certificates, out of tolerance reports, deviations, and SCARs as necessary.•\tAssist with the development and implementation of company SOPs as assigned.•\tPerform document control and training activities as assigned.•\tRequires an ability to complete cGMP documentation accurately, in accordance with standard operating procedures, and in a timely manner.•\tRequires an ability to work independently to accomplish given tasks within given timelines.•\tRequires an ability to multitask and adjust to changing priorities.•\tMust report any deviations or nonconformities immediately to a Manager or Director.•\tOther duties as assigned.
\t\t\t\t\tSkills
\t\t\t\t\tQuality control, Gmp, Laboratory, Troubleshooting, Quality assurance, Microbiology
\t\t\t\t\tTop Skills Details
\t\t\t\t\tQuality control,Gmp,Laboratory
\t\t\t\t\tAdditional Skills & Qualifications
\t\t\t\t\t•\tAssociate’s Degree in related field or equivalent work experience•\t6 months to a 1 or more years of previous related experience Industry preferred•\tGood communication and organizational skills and ability to multitask.•\tPrior experience with ISO 13485 and 21 CFR 820 a plus.•\tThrives in a fast-paced, collaborative environment, efficiently works under pressure, within deadlines or other time essential constraints
\t\t\t\t\tExperience Level
\t\t\t\t\tEntry Level
Pay and Benefits
The 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 10, 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.