Manufacturing Associate

Manufacturing Associate | Biopharmaceutical Manufacturing Join a growing biopharmaceutical manufacturing team where you'll play a key role in supporting production operations, maintaining quality standards, and ensuring products are manufactured safely and efficiently in a GMP-regulated environment. This is an excellent opportunity for someone looking to build or grow a career in biotechnology manufacturing while gaining hands‑on experience with production processes, quality systems, batch documentation, and cleanroom operations. Responsibilities Execute manufacturing work instructions and apply job skills to complete daily production activities. Maintain accurate inventory records and batch documentation in accordance with GMP and Good Documentation Practices (GDP). Inspect finished products to ensure compliance with quality specifications. Assist with batch record review and reconciliation activities. Support preventative maintenance activities and equipment readiness. Adhere to Quality Management Systems (QMS) and assist with Nonconformance and CAPA activities. Identify and communicate manufacturing, quality, or safety issues requiring escalation. Maintain a clean, organized, and compliant manufacturing environment. Follow all company policies related to GMP compliance, safety, training, and cleanroom gowning requirements. Achieve full training qualification and assist in training team members as needed. Qualifications High School Diploma or equivalent required. Minimum of 1 year of experience in manufacturing, production, operations, laboratory, or a related environment. Experience working in a cGMP-regulated environment is highly preferred. Strong understanding of GMP principles, quality systems, and manufacturing documentation. Ability to learn new processes, equipment, software, and production systems quickly. Strong attention to detail and documentation accuracy. Effective communication skills and the ability to work collaboratively within a team environment. Ability to recognize issues, make sound decisions, and elevate concerns appropriately. Preferred Experience Biopharmaceutical or pharmaceutical manufacturing Inventory control and materials management Batch record review and documentation Quality Management Systems (QMS) Cleanroom operations and aseptic gowning GMP-regulated production environments Why Join? Opportunity to gain experience with a growing biopharmaceutical organization. Exposure to GMP manufacturing, quality systems, and production operations. Collaborative team environment with hands‑on training and career development opportunities. Build valuable experience within the biotechnology and pharmaceutical industry. Work with experienced professionals committed to quality, safety, and operational excellence. Job Type & Location This is a Contract position based out of Plainville, MA. Pay And Benefits The pay range for this position is $27.00 - $28.00/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) Application Deadline This position is anticipated to close on Nov 23, 2026. Workplace Type This is a fully onsite position in Plainville,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 View email address on click.appcast.io 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. #J-18808-Ljbffr ACTalent