Manufacturing Associate

Job Title:

Manufacturing Associate (Band Level 3) Job Description This Manufacturing Associate role operates at a senior technician level, guiding daily manufacturing operations within a cGMP biopharmaceutical environment. You will mentor junior technicians, act as a subject matter expert for at least one unit operation, and perform complex tasks that require sound judgment and strong scientific understanding. The position focuses on safe, compliant, and efficient execution of manufacturing processes while supporting continuous improvement initiatives and maintaining a clean, controlled production environment. Responsibilities Provide day-to-day guidance to other technicians and help drive efficient manufacturing operations on the production floor. Mentor new employees, support their onboarding, and act as a senior technician and role model in the manufacturing suites. Perform complex manufacturing tasks that require independent judgment and effective resolution of process issues. Maintain strict compliance with standard operating procedures (SOPs), Good Manufacturing Practices (GMPs), and all safety guidelines. Serve as a subject matter expert (SME) for at least one unit operation, including obtaining and analyzing batch samples to support process control and decision-making. Oversee manufacturing equipment upkeep by performing basic maintenance, troubleshooting issues, and escalating problems when needed. Review, revise, and author batch records and SOPs to ensure documentation remains accurate, clear, and compliant. Participate in Practical Process Improvement (PPI) and other continuous improvement initiatives to enhance process efficiency and quality. Identify issues that require escalation, clearly communicate them to appropriate stakeholders, and execute decisions following escalation. Provide constructive feedback and coaching to team members to support performance improvement and professional growth. Participate in daily performance huddles and assist with developing and maintaining process schedules. Maintain a clean, organized, and safe work environment in accordance with company policies and regulatory expectations. Follow all company policies related to safety, training, Good Documentation Practices (GDP), and cleanroom gowning requirements. Spend approximately 90% of working time in manufacturing suites performing hands-on production activities. Use computers daily to complete documentation, review instructions, and support data entry and analysis. Safely handle materials and conditions that may include dry ice, liquid nitrogen cryogenics, hazardous agents, and infectious agents, while adapting to marked changes in temperature. Essential Skills High school diploma or equivalent required. Minimum of 2 years of work experience in a manufacturing, operations, production, laboratory, or closely related setting. Full understanding of Good Manufacturing Practices (GMP) and strong knowledge of biopharmaceutical manufacturing processes. Demonstrated ability to lead, guide, and mentor junior staff in a production or laboratory environment. Strong grasp of the underlying science behind manufacturing processes, with the ability to interpret process data and inputs. Excellent verbal and written communication skills to interact effectively with cross-functional teams and document work accurately. Strong autonomous problem-solving and investigative skills, with the ability to identify root causes and propose practical solutions. Solid understanding of cleanroom concepts and controlled environment operations. Ability to follow directions and procedures precisely while contributing effectively in a team-oriented environment. Strong attention to detail and a consistent drive to complete tasks in a timely, accurate, and safe manner. Ability to apply knowledge of Good Manufacturing processes, equipment, instrumentation, and procedures in daily operations. Physical ability to stand, walk, and perform manual tasks for extended periods; regularly use hands to handle or feel materials and equipment. Capability to aseptically gown and/or sterile gown as required for cleanroom entry and operations. Ability to frequently walk and stoop, kneel, or crouch (approximately 80% of the time) and ascend or descend stairs (approximately 20% of the time). Ability to lift up to 50 pounds and sit for up to 4 hours as needed. Adequate close vision and ability to adjust focus for detailed tasks and documentation. Comfort with daily computer use for documentation and process-related activities. Willingness and ability to work safely with PPE around dry ice, liquid nitrogen cryogenics, hazardous agents, infectious agents, and varying temperatures. Additional Skills & Qualifications Experience working in a cGMP manufacturing environment is preferred. Background in production, GMP operations, cleanroom manufacturing, packaging, or sanitization is highly beneficial. Experience participating in or supporting Practical Process Improvement (PPI) or similar continuous improvement programs. Familiarity with authoring, reviewing, and revising batch records and SOPs in a regulated environment. Comfort working in a fast-paced, team-based setting with changing priorities and multiple concurrent tasks. Why Work Here? You will join a highly collaborative and process-driven environment where safety, quality, and continuous improvement are core values. The organization emphasizes teamwork, mentorship, and professional development, giving you the opportunity to grow your technical expertise while contributing to meaningful biopharmaceutical products. You will work with advanced manufacturing processes in a structured setting that values clear communication, strong documentation practices, and a culture of accountability and respect. Work Environment This role is primarily based in controlled manufacturing suites, where you will spend about 90% of your time performing hands-on production activities. The environment follows cGMP standards and cleanroom protocols, requiring aseptic and sterile gowning and consistent use of Personal Protective Equipment (PPE). Work involves regular standing, walking, and manual handling, including frequent stooping, kneeling, or crouching and occasional stair climbing. You may lift up to 50 pounds and sit for limited periods when completing documentation or computer-based tasks. Daily computer use is required for batch records, SOP review, and data entry. The facility may involve exposure to dry ice, liquid nitrogen cryogenics, hazardous and infectious agents, and noticeable temperature changes, all managed under strict safety procedures. The dress code emphasizes cleanroom-appropriate attire and PPE to maintain a safe, compliant, and contamination-controlled workspace. Job Type & Location This is a Contract position based out of Plainville, MA. Pay and Benefits The pay range for this position is $31.00 - $34.00/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 Plainville,MA.

Application Deadline This position is anticipated to close on Jul 6, 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.