Job Title: Quality Control Technician

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. Requires an ability to complete cGMP documentation accurately, in accordance with standard operating procedures, and in a timely manner. Requires an ability to work independently to accomplish given tasks within given timelines. Requires an ability to multitask and adjust to changing priorities. Must report any deviations or nonconformities immediately to a Manager or Director. Other duties as assigned.

Responsibilities

• Perform quality control testing in the QC Testing Laboratory.
• Understand and operate all laboratory instrumentation and equipment.
• Perform maintenance, clean benchtops, hoods, and laboratories, and dispose of biohazardous waste.
• Organize and handle testing samples and maintain testing inventory.
• Assist with 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.
• 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 given tasks within timelines.
• Multitask and adjust to changing priorities.
• Report any deviations or nonconformities immediately to a Manager or Director.
• Other duties as assigned.

Essential Skills

• Quality control
• GMP
• Laboratory experience
• Quality assurance
• Microbiology
• Troubleshooting

Additional Skills & Qualifications

• Associate’s Degree in related field or equivalent work experience.
• 6 months to 1 or more years of previous related experience preferred.
• Good communication and organizational skills.
• Ability to multitask.
• Prior experience with cGMP and 21 CFR 820 a plus.
• Ability to work in a fast-paced, collaborative environment.
• Efficiently work under pressure within deadlines.

Work Environment

1st Shift: Monday - Friday 8:00am - 4:30pm, overtime as needed. Breakfast provided every Friday. Opportunity to grow from within. Potential for raise after the contract period (not guaranteed). Summer cookouts and ice cream socials. Small company feel with strong job security backed by a large corporation. Not micromanaged.

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 Mar 21, 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.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Salary : $20 - $22