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Biomanufacturing Associate Jobs in Lowell, MA (NOW HIRING)

... and biomanufacturing. Together, these investments reflect the breadth of our focus across both ... The Associate will work directly with founders and company leaders across stages, from early ...

... and biomanufacturing. Together, these investments reflect the breadth of our focus across both ... The Associate will work directly with founders and company leaders across stages, from early ...

Resilience is a technology-focused biomanufacturing company that's changing the way medicine is ... Associate's or Bachelor's degree in Business Administration, Communications, or a related field

Resilience is a technology-focused biomanufacturing company that's changing the way medicine is ... Associate's or Bachelor's degree in Business Administration, Communications, or a related field

Resilience is a technology-focused biomanufacturing company that's changing the way medicine is ... Associate's or Bachelor's degree in Business Administration, Communications, or a related field

Resilience is a technology-focused biomanufacturing company that's changing the way medicine is ... Associate's or Bachelor's degree in Business Administration, Communications, or a related field

Biomanufacturing Associate information

See Lowell, MA salary details

$26.8K

$140K

$307.9K

How much do biomanufacturing associate jobs pay per year?

As of Aug 24, 2026, the average yearly pay for biomanufacturing associate in Lowell, MA is $140,046.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,700.00 and $210,800.00 per year, depending on experience, location, and employer.

What is a biomanufacturing associate?

A Biomanufacturing Associate is a professional who assists in the production of biopharmaceutical products, such as vaccines and therapeutic proteins, using biological systems like living cells. They are responsible for operating equipment, monitoring processes, following strict safety and quality protocols, and documenting production activities. Biomanufacturing Associates play a vital role in ensuring that products are made efficiently and meet regulatory standards in highly controlled environments.

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

To thrive as a Biomanufacturing Associate, you need a solid understanding of biotechnology, aseptic techniques, and good manufacturing practices (GMP), often supported by a degree in biology, chemistry, or related fields. Familiarity with bioprocessing equipment, batch record documentation, and quality control systems is typically required. Attention to detail, teamwork, and strong problem-solving skills help individuals excel in this role. These competencies ensure safe, consistent, and high-quality production of biopharmaceutical products in regulated environments.

What are some common challenges faced by biomanufacturing associates, and how can they be addressed?

Biomanufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), handling complex bioprocess equipment, and meeting tight production deadlines. These challenges can be managed by staying organized, following detailed protocols, and actively participating in ongoing training. Collaborating closely with team members and supervisors also helps ensure that any deviations or equipment issues are quickly identified and resolved, maintaining product quality and safety standards.

What is the difference between Biomanufacturing Associate vs Quality Control Technician?

AspectBiomanufacturing AssociateQuality Control Technician
Required CredentialsAssociate degree in biology, chemistry, or related fieldAssociate degree or certification in quality control or laboratory techniques
Work EnvironmentManufacturing floor, production areasLaboratories, testing facilities
Employer & Industry UsageBiotech, pharmaceutical manufacturingPharmaceutical, biotech, and medical device companies

Biomanufacturing Associates focus on the production process, operating equipment, and ensuring manufacturing runs smoothly. Quality Control Technicians primarily perform testing and inspections to ensure product quality. While both roles require technical skills and work in related environments, their core responsibilities differ, with manufacturing associates involved in production and QC technicians in quality assurance.

What are popular job titles related to Biomanufacturing Associate jobs in Lowell, MA?

For Biomanufacturing Associate jobs in Lowell, MA, the most frequently searched job titles are:

What job categories do people searching Biomanufacturing Associate jobs in Lowell, MA look for?

The top searched job categories for Biomanufacturing Associate jobs in Lowell, MA are:

What cities near Lowell, MA are hiring for Biomanufacturing Associate jobs?

Cities near Lowell, MA with the most Biomanufacturing Associate job openings:

Infographic showing various Biomanufacturing Associate job openings in Lowell, MA as of August 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $140,046 per year, or $67.3 per hour.

Biomanufacturing Associate II (Contract, Monday-Friday)

ElevateBio

Waltham, MA • On-site

$38 - $52/hr

Full-time

Posted 10 days ago


Job description

ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.
The Role:
ElevateBio is looking for a dynamic individual to join and, contribute to building the manufacturing operations team at our BaseCamp facility. The incumbent will ultimately perform routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as CAR-Ts, iPSCs, Adeno-Associated Virus (AVV) and Lentivirus (LV). The individual should be a motivated self-starter eager to contribute to building a manufacturing operation unparalleled in its capabilities and expertise, have a willingness and aptitude for adoption of new technology, an ability to build relationships and work effectively in a cross-functional team, and commitment to the highest safety and quality standards.
Here's What You'll Do:
  • Perform and lead routine right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, cryopreservation, upstream processing, downstream processing, aseptic fill finish and final product visual inspection.
  • Perform manufacturing/operations start-up activities including but not limited to authoring SOPs, batch records, reports, risk assessments, material ordering/management.
  • Provide training to team on set-up and use of equipment, process and material flows, as assigned.
  • Ensure clean rooms are maintained in an organized and ready state.
  • Provide constructive input on teams for the selection and set-up of equipment, process and material flows, etc.
  • Create and maintain training materials and curricula that support continuous improvement in the cGMP manufacture of cell therapy products.
  • Work effectively with cross functional teams comprised of process sciences, development, facilities & engineering, tech ops, quality control, quality assurance, to ensure right-first-time technology transfer.
  • Work closing with Quality Assurance and Process Sciences to proactively resolve issues such as deviations, CAPAs, Change Controls.
  • Commitment to the highest safety and quality standards in service of our colleagues and patients.
  • Generate and manage batch records, run reports, batch data, etc. for manufacturing and scale-up activities.
  • Proactively identify opportunities for improvements in process, safety, quality, and cost

Requirements:
  • Bachelor's degree in biological science(s) field or related engineering with:
    • For BMA I's, 0-1+ years of experience in cGMP biotech manufacturing, preferably cell and gene therapies
    • For BMA II's, 2+ years of experience in cGMP biotech manufacturing, preferably cell and gene therapies
    • For BMA III's, 3-6+ years of experience in cGMP biotech manufacturing, preferably cell and gene therapies
    • For BMA IV's 4-6+ years of experience in cGMP biotech manufacturing, preferably cell and gene therapies
  • 2+ years of experience in project leadership is preferred.
  • Experience with some or all of the following: cGMP manufacture and/or process development for CAR T, TCR, NK, cellular therapies, AAV, LV, RV.
  • Advanced understanding of primary cell culture and experience with equipment such as CliniMACS Plus, CliniMACS Prodigy, LOVO, bioreactors (single-use and fixed-bed), chromatography skids, TFF (hollow-fiber and flat-sheet) and WAVE bioreactors such as Xuri, G-Rex system.
  • Outstanding communication skills (verbal and written)
  • Excellent computer and word processing skills including Microsoft Excel, PowerPoint, and Word.
  • Demonstrate proficiency in aseptic technique and/or processing.
  • Ability to function in dynamic environment and balance multiple priorities simultaneously.

Work Schedule:
  • Monday-Friday, 9:00 am - 5:00 pm
  • Must be available to overtime on weekdays and holidays as needed.

Physical Requirements:
  • Employee will frequently stand, walk, bend, stretch for extended periods.
  • Routinely carry up to 25 pounds and up to 50 pounds.
  • Routinely push, pull, bend, kneel, twist, and climb step ladders while wearing PPE.
  • Routine repetitive use of arms/wrist/hands.
  • Ability to work nights, weekends, holidays as needed to support business needs.

The budgeted range for these positions are $38/hour - $52/hour dependent on level hired. This range is a good faith estimate of the expected hourly range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.
ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.