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Quality Assurance Associate

  • Norwood, MA, United States

$32 to $35 USD / hour

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Job details

Pay
$32 to $35 USD / hour
Experience
0-2 years of experience in a GMP-regulated manufacturing, biotechnology, pharmaceutical, laboratory, or quality environment.
Posting language
English
Posted

Original job description

Associate Quality Assurance Specialist Location: Norwood, MA Schedule: Full-Time - 6-Month Contract Our client, a growing biotechnology company, is seeking an Associate Quality Assurance Specialist to support GMP manufacturing operations. This is an excellent opportunity for recent graduates or early-career professionals looking to build a career in Quality Assurance within the biotech or pharmaceutical industry.The individual in this role will partner closely with Manufacturing and cross-functional teams to ensure operations are conducted in compliance with GMP requirements and quality standards while providing real-time support on the manufacturing floor.Key Responsibilities

  • Provide quality support for day-to-day manufacturing operations, including documentation review, line clearances, and changeover activities.
  • Partner with Manufacturing teams to help resolve quality, equipment, and process-related issues in real time.
  • Support quality decision-making and escalate concerns when appropriate.
  • Identify and communicate quality and compliance risks within manufacturing processes and systems.
  • Review and approve facility alarms, work orders, and return-to-service documentation.
  • Ensure manufacturing documentation is completed accurately and in accordance with GMP requirements.
  • Maintain compliance with company procedures, quality systems, and regulatory standards.
  • Collaborate with cross-functional groups to support production goals and continuous improvement initiatives.

Qualifications

  • Bachelor's degree in Biology, Chemistry, Biochemistry, Biomedical Engineering, Bioengineering, Chemical Engineering, or a related scientific discipline.
  • 0-2 years of experience in a GMP-regulated manufacturing, biotechnology, pharmaceutical, laboratory, or quality environment.
  • Knowledge of GMP regulations and documentation practices is preferred.
  • Strong attention to detail and organizational skills.
  • Excellent verbal and written communication abilities.
  • Ability to work effectively in a fast-paced manufacturing environment.
  • Strong problem-solving skills and willingness to learn.

If interested, please reach out to Lindsee Allienello at lallienello @ actalentservices.com. Job Type & LocationThis is a Contract position based out of Norwood, MA. Pay and BenefitsThe pay range for this position is $32.00 - $35.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.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) Job Type & LocationThis is a Contract position based out of Norwood, MA. Application DeadlineThis position is anticipated to close on Nov 27, 2026. Workplace TypeThis is a fully onsite position in Norwood,MA.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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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