Quality Assurance Associate

Work Arrangement: 100% OnsiteSchedule: MondayFriday, 8:30 AM5:00 PM or 6:30 AM3:00 PM, with a 30-minute meal breakContract Length: 12 months with potential for extension Position Overview We are seeking a Plant Quality Assurance Specialist to provide on-the-floor quality oversight within a regulated biopharmaceutical manufacturing environment. This individual will partner closely with Facilities & Engineering, Process Development, Incoming Quality, Warehouse, and Manufacturing teams to ensure operations comply with cGMP requirements, internal procedures, and applicable regulatory standards.

Key Responsibilities

• Provide quality oversight for Facilities & Engineering, Incoming Quality, Warehouse, Raw Material Sampling, Process Development, and Manufacturing activities.
• Ensure facilities, equipment, materials, processes, and products meet cGMP and regulatory requirements.
• Review and approve work orders and job plans within Maximo.
• Review GMP documentation, including logbooks, electronic and paper forms, pest-control documentation, and related reports.
• Review and approve Manufacturing Execution System (MES) records, including electronic batch records.
• Support the management and oversight of rejected materials.
• Review and approve DeltaV audit trail entries.
• Ensure deviations from established procedures are properly documented and handled according to approved quality processes.
• Collaborate cross-functionally to ensure quality-related activities and assigned tasks are completed accurately and on time.
• Proactively identify and escalate potential quality, compliance, or safety risks.
• Maintain required training and documentation to ensure continued compliance.
• Spend approximately 25% of the shift in cleanroom environments, following appropriate gowning and aseptic practices.

Preferred Qualifications

• Bachelor's degree in Life Sciences, Biology, Chemistry, Biotechnology, Engineering, or a related field.
• Minimum of 2 years of experience in Quality or Manufacturing within a regulated environment.
• Strong understanding of cGMP principles and regulatory requirements.
• Experience reviewing GMP documentation, manufacturing records, deviations, work orders, or quality records.
• Experience with systems such as Maximo, MES, Veeva Vault, or similar quality/manufacturing systems preferred.
• Proficiency with Microsoft Outlook, Word, Excel, PowerPoint, and Teams.
• Strong written and verbal communication skills.
• Ability to collaborate effectively across Quality, Manufacturing, Engineering, and other technical teams.
• Ability to prioritize multiple responsibilities and make sound decisions in a fast-paced environment with limited oversight.

Job Type & LocationThis is a Contract position based out of West Greenwich, RI. Pay and BenefitsThe pay range for this position is $25.00 - $30.00/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 West Greenwich, RI. Application DeadlineThis position is anticipated to close on Nov 25, 2026. Workplace TypeThis is a fully onsite position in West Greenwich,RI.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.