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Biotech Manufacturing Associate Jobs in Boston, MA

TScan Therapeutics

Manufacturing Associate II

Waltham, MA · On-site

$95K - $122K/yr

TScan Therapeutics is a clinical-stage biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are hiring Manufacturing Associate I-II ...

Integrated Resources INC

Process Associate

Andover, MA · On-site

Required a Manufacturing Process Technician in a large scale biotech manufacturing facility This position is a temporary contract working on a 12 hour shift (6am - 6pm.) Includes some weekend work ...

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All JobsBiotech Manufacturing Associate JobsBiotech Manufacturing Associate Jobs in Boston, MA

Biotech Manufacturing Associate information

See Boston, MA salary details

$13

$22

$36

How much do biotech manufacturing associate jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for biotech manufacturing associate in Boston, MA is $22.67, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $25.38 per hour, depending on experience, location, and employer.

What is a biotech manufacturing associate?

Biotech Manufacturing Associates are professionals who work in the production of biotechnology products, such as pharmaceuticals, vaccines, and other biologically derived materials. They are responsible for operating equipment, following strict protocols, and maintaining sterile environments to ensure product quality and safety. Their duties often include preparing materials, monitoring production processes, troubleshooting equipment issues, and documenting all activities according to regulatory standards. This role is essential in ensuring that biotech products are manufactured efficiently and meet both industry and government regulations.

What are the key skills and qualifications needed to thrive as a biotech manufacturing associate?

To thrive as a Biotech Manufacturing Associate, you typically need a background in biology, chemistry, or a related field, along with experience in GMP-regulated environments. Familiarity with bioprocessing equipment, laboratory instrumentation, and documentation systems such as batch records is crucial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in this collaborative and regulated field. These skills ensure the consistent production of safe, high-quality biotech products while maintaining compliance with industry standards.

What are some common challenges faced by biotech manufacturing associates, and how can they be managed effectively?

Biotech Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and working under tight production deadlines. Effective management of these challenges involves strong attention to detail, proactive communication with cross-functional teams such as quality assurance and engineering, and continuous learning to stay updated on new protocols and technologies. Developing problem-solving skills and embracing a collaborative mindset can also help associates consistently contribute to high-quality production outcomes.

What is the difference between Biotech Manufacturing Associate vs Laboratory Technician?

AspectBiotech Manufacturing AssociateLaboratory Technician
CredentialsHigh school diploma or equivalent; some roles may require associate degreeHigh school diploma or equivalent; some roles may require associate degree or certification
Work EnvironmentManufacturing floor, production lines, cleanroomsLaboratories, research facilities, testing environments
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, quality control, testing labs

While both roles support biotech operations, a Biotech Manufacturing Associate primarily works on production and manufacturing processes in a cleanroom environment, focusing on assembling, monitoring, and maintaining manufacturing equipment. In contrast, a Laboratory Technician typically conducts experiments, tests, and quality control procedures in a laboratory setting. Both roles require attention to detail and adherence to safety protocols, but their daily tasks and work environments differ significantly.

What are popular job titles related to Biotech Manufacturing Associate jobs in Boston, MA?

For Biotech Manufacturing Associate jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Biotech Manufacturing Associate jobs in Boston, MA look for?

The top searched job categories for Biotech Manufacturing Associate jobs in Boston, MA are:

What cities near Boston, MA are hiring for Biotech Manufacturing Associate jobs?

Cities near Boston, MA with the most Biotech Manufacturing Associate job openings:

Biotech Manufacturing Associate jobs near you
Infographic showing various Biotech Manufacturing Associate job openings in Boston, MA as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 26% Part Time, 1% Temporary, and 3% Contract. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $47,144 per year, or $22.7 per hour.

Biopharma Manufacturing Associate II

Astellas Pharma, Inc.

Westborough, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 26 days ago

Job description

Biopharma Manufacturing Associate II
About Astellas
Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need. Learn more at Astellas.com.
Are you driven to make a real difference in the lives of patients?
We're seeking passionate individuals who thrive in dynamic environments, embrace new ideas, and aren't afraid to take intelligent risks. People who act with unwavering integrity and are deeply committed to making a tangible impact.
Purpose & Scope
The Biopharma Manufacturing Associate II will be a key contributor to manufacturing readiness and future operational output of the manufacturing facility. The role will initially support ongoing commissioning and validation activities as the site works towards GMP production readiness and will provide overall manufacturing operations support that includes yet is not limited to; equipment testing, SOP/batch record generation, and validation protocol execution support. Once commissioning and validation is complete, the role will be responsible for executing a combination of engineering and GMP clinical batches with supporting staff. This role, as part of the Manufacturing division, will be an integral contributor tasked with building a diverse and technically strong team for future successful GMP operations.
Role and Responsibilities
  • Perform all manufacturing operations under cGMP/ISO requirements
  • Display understanding of Upstream process theory (e.g., cell thawing, passages, and harvesting) equipment operation, and aseptic processing
  • Assist with the installation, commissioning, and validation of equipment within single use facility
  • Adhere to manufacturing procedures and documentation as well as identifying clarifications or updates when required
  • Perform legible, clear, and concise data entry into batch records, logbooks, and all other ancillary controlled forms used in a cGMP process
  • Maintain a high level of quality and compliance with regards to all aspects of manufacturing
  • Assist/write SOPs (standard operating procedures), batch records, and other GMP documentation
  • Display ability to identify and escalate potential GMP issues, as required
  • Available to participate in flexible shifts (Day, Swing, Weekends, Holidays) as directed by the facility start up and future production schedules
  • Assist in the evaluation and incorporation of new technologies

Required Qualifications
Education:
  • BS / BA in Chemical/ Biological Engineering or Life Sciences or Associate's Degree in science or related field with 1+ years of industry experience.

Experience:
  • Experience in maintaining detailed records and ability to assist in document revisions
  • Experience in cell culture with excellent aseptic technique
  • Strong skill on biological laboratory math
  • Understanding of cGMPS as related to commercial and clinical operations
  • Strong communicator with ability to work effectively both independently and as part of a team • Developing problem-solving skills
  • Strong computer skills including MS Office (Word, Excel) and proven ability to establish and maintain effective working relationships with team members and managers
  • Models our Core Values: Be Bold, Care Deeply, Get Stuff Done - is experienced as someone who exemplifies the culture we want to create; operates with transparency; is trusted
  • Will support and demonstrate quality standards to ensure data of highest quality and will be expected to perform other duties and/or special projects, as assigned

Preferred Qualifications
  • BioWork Certification or related type certifications are a plus along with technical understanding of a biotech manufacturing facility
  • Knowledge of upstream process and aseptic technique
  • Experience with single-use technologies
  • Understanding of FDA regulations
  • Experience with continuous improvement platforms and history of identifying changes with positive impact to safety, product quality, and/or operational efficiency
  • Ability to clearly define events and associated process conditions during nonconformance or safety escalation efforts
  • Ability to multi-task, be flexible and to thrive in a fast-paced environment, as well as the capacity to handle uncertainty and changing priorities

Location and Working Environment
  • This position is based in Westborough, MA and will require on-site work.
  • This role frequently requires long periods of sitting, standing and use of hands and regular motion to include bending, stooping, regular reaching over head activities, and independent mobility to lift to 25lbs.
  • This role supports the cleanroom. Gowning in to the cleanroom is expected.
  • This is a 100% on-site role working in a cGMP regulated manufacturing facility.
  • This roles requires to work in shifts - 4 x 10s, 12 hrs rotating, administrative or 2nd, depending on the business needs. Shift shall be assigned upon recruitment and are subject to change upon hire.
  • Assigned shift schedules is subject to change with or without notice based on critical operational needs.
  • Weekend work is often scheduled to support staffing and operational needs.
  • On occasion, this role may travel to other Astellas Biopharma Manufacturing facilities (0-5%)

What awaits you at Astellas?
  • Global collaboration: Become part of a connected global business of like-minded life science leaders, all dedicated to improving patients' lives worldwide.
  • Real-world patient impact: Contribute to transformative therapies that reach patients around the world, knowing your work makes a difference every day.
  • Relentless Innovation: Join a company at the forefront of scientific breakthroughs, where you'll have the opportunity to shape the future of healthcare.
  • A Culture of Growth: Chart your own course within a supportive environment that values your contributions, champions your development, and empowers you to pursue your passions.

Our Organizational Values and Behaviors
Values: Innovation, Integrity and Impact sit at the heart of what we do.
Behaviors: We come together as 'One Astellas', working with courage and a sense of urgency. We are outcome focused and consistently take accountability for our personal contribution.
Salary Range
$32.38-$46.25 (Final compensation will be determined based on a variety of factors, including but not limited to skills, experience and organizational equity considerations.)
Benefits:
  • Medical, Dental and Vision Insurance
  • Generous Paid Time Off options, including Vacation and Sick time, plus national holidays including year-end shut down
  • 401(k) match and annual company contribution
  • Company paid life insurance
  • Annual Corporate Bonus and Quarterly Sales Incentive for eligible positions
  • Long Term Incentive Plan for eligible positions
  • Company fleet vehicle for eligible positions
  • Referral bonus program

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