Job Title: Manufacturing Associate
Job Description
The Manufacturing Associate supports biopharmaceutical production by executing defined work instructions, operating manufacturing equipment, and maintaining accurate documentation in a regulated GMP environment. This role focuses on performing semi-routine manufacturing activities, inspecting finished products for quality, and contributing to a safe, clean, and compliant production area. The Manufacturing Associate also assists with training peers, supports nonconformance and CAPA activities, and helps ensure consistent adherence to quality and safety standards.
Responsibilities
Execute detailed work instructions and apply job-specific skills to complete manufacturing assignments accurately and on time.
Work on semi-routine manufacturing tasks, seeking instruction and clarification for new or unfamiliar processes as needed.
Achieve full training status on assigned operations and assist in training and mentoring other staff members.
Operate biopharmaceutical manufacturing equipment in accordance with established procedures and GMP requirements.
Maintain accurate inventory records and batch documentation, ensuring data integrity and traceability.
Inspect finished products to verify adherence to specifications and quality standards, and document inspection results.
Assist with batch record reconciliation to ensure completeness, accuracy, and compliance with GMP requirements.
Support preventative maintenance tasks on equipment and systems as directed, helping to maintain reliable operations.
Adhere to Quality Management Systems and assist with closure of nonconformances and CAPA activities.
Identify issues or deviations that require escalation and promptly communicate them to lead operators or area management.
Maintain a clean, organized, and safe work environment in manufacturing suites and supporting areas.
Follow all company policies and procedures, including safety guidelines, training requirements, Good Documentation Practices (GDP), and cleanroom gowning standards.
Safely perform activities to prevent product releases, accidents, and injuries, including proper handling of hazardous materials and cryogenic substances.
Read, write, and review operational and GMP documentation for extended periods to ensure accuracy and completeness.
Use computer systems and software tools daily to enter data, review records, and support manufacturing operations.
Spend the majority of working time (approximately 90%) in manufacturing suites, performing hands-on production activities.
Essential Skills
High school diploma or equivalent.
Minimum of 1 year of work experience in manufacturing, operations, production, laboratory setting, or a related field.
Technical expertise in biopharmaceutical manufacturing equipment, principles, and processes.
Strong understanding of current Good Manufacturing Practices (GMP) and safety standards.
Ability to function effectively in a dynamic environment and balance multiple priorities.
Proficiency in learning and using new software and tools to support manufacturing operations and documentation.
Ability to make decisions for moderately complex GMP manufacturing activities with minimal to moderate supervision.
Ability to recognize, understand, and appropriately respond to situations requiring further evaluation and escalate to lead operators or management.
Effective written and verbal communication skills for interacting with peers, lead associates, and area management.
Understanding of operational documents to ensure GMP compliance, accuracy, and completeness.
Ability to safely perform activities to prevent product releases, accidents, and injuries.
Ability to aseptically gown and/or sterile gown as required for cleanroom operations.
Ability to write, read, and review documentation for extended periods while maintaining attention to detail.
Ability to meet specific vision requirements, including close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.
Ability to regularly talk and hear, and frequently sit and stand for extended periods to support production activities.
Ability to occasionally lift, walk, use hands to finger, handle or feel, reach with hands and arms, and stoop, kneel, or crouch as required by the role.
Comfort with daily computer use for documentation, data entry, and system navigation.
Additional Skills & Qualifications
Preferred experience working in a cGMP-regulated environment.
Experience working in production, cleanroom, packaging, or other controlled manufacturing settings.
Familiarity with biopharmaceutical production processes and cleanroom operations.
Experience handling or working around dry ice, liquid nitrogen cryogenics, hazardous agents, and infectious agents.
Ability to adapt to marked changes in temperature when working with cryogenics or controlled environments.
Strong attention to detail and commitment to following established procedures and documentation standards.
Why Work Here?
This opportunity offers the chance to work in a highly regulated, cutting-edge biopharmaceutical manufacturing environment where quality, safety, and continuous improvement are central values. You will develop specialized technical skills, gain hands-on experience with advanced manufacturing equipment, and contribute directly to the production of critical therapies. The organization supports ongoing training, encourages collaboration across teams, and promotes a culture of accountability, learning, and professional growth.
Work Environment
The role is based primarily in GMP manufacturing suites, with approximately 90% of time spent in these controlled environments. Team members work around biopharmaceutical production equipment, cleanroom areas, and packaging operations while following strict GMP, safety, and Good Documentation Practices. Personal Protective Equipment (PPE) is provided and required, including cleanroom gowning; aseptic and sterile gowning may be required depending on the operation. Closed-toe shoes are required, and GMP regulations prohibit certain personal adornments such as visible piercings and nail polish while in controlled areas. The work involves regular use of computers for documentation and system access, as well as frequent sitting and standing for extended periods. Employees may occasionally lift, walk, reach, handle materials, and stoop, kneel, or crouch as part of their duties. The environment may involve working with dry ice, liquid nitrogen cryogenics, hazardous and infectious agents, and exposure to noticeable changes in temperature, all under strict safety protocols to ensure a safe and compliant workplace.
Job Type & Location
This is a Contract position based out of Plainville, MA.
Pay and Benefits
The pay range for this position is $31.05 - $34.50/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 Plainville,MA.
Application Deadline
This position is anticipated to close on Jun 30, 2026.
About Aerotek
Aerotek® Inc. provides staffing and services solutions in manufacturing, logistics, construction, aviation, facilities and maintenance. We provide the expertise, solutions and people required to rise to the challenges of North American industry. Headquartered in Hanover, Md., Aerotek operates a unified network of over 200 offices across North America, supporting more than 18,000 clients each year. Aerotek is an Allegis Group company, the global leader in workforce and business solutions. To learn more, visit: Aerotek.com | 1-888-AEROTEK.
Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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.
