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Biotech Manufacturing Associate Jobs in Boston, MA

Oligo Factory

Purification Associate

Holliston, MA · On-site

Company Description Oligo Factory is a Massachusetts-based manufacturer specializing in custom DNA ... Bachelor's degree in Biology, Chemistry, Biochemistry, Biotechnology, Chemical Engineering, or a ...

Sanofi EU

Senior Manufacturing Technician

Lynn, MA · On-site

$24 - $32/hr

High School diploma/GED with a minimum of 1 year of experience in cGxP manufacturing environment, or Biotech Certificate or Biotech associate's degree with no prior experience. ​ Preferred ...

Sanofi EU

Senior Manufacturing Technician

Brockton, MA · On-site

$24 - $32/hr

High School diploma/GED with a minimum of 1 year of experience in cGxP manufacturing environment, or Biotech Certificate or Biotech associate's degree with no prior experience. ​ Preferred ...

Sanofi EU

Senior Manufacturing Technician

Quincy, MA

$24 - $32/hr

High School diploma/GED with a minimum of 1 year of experience in cGxP manufacturing environment, or Biotech Certificate or Biotech associate's degree with no prior experience. ​ Preferred ...

Sanofi EU

Senior Manufacturing Technician

Boston, MA · On-site

$24 - $32/hr

High School diploma/GED with a minimum of 1 year of experience in cGxP manufacturing environment, or Biotech Certificate or Biotech associate's degree with no prior experience. ​ Preferred ...

Sanofi EU

Senior Manufacturing Technician

Lowell, MA · On-site

$24 - $32/hr

High School diploma/GED with a minimum of 1 year of experience in cGxP manufacturing environment, or Biotech Certificate or Biotech associate's degree with no prior experience. ​ Preferred ...

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

Biotech Manufacturing Associate information

See Boston, MA salary details

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How much do biotech manufacturing associate jobs pay per hour?

As of Sep 8, 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 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $47,144 per year, or $22.7 per hour.

Downstream Manufacturing Associate III (Wed-Sat 4/3 Overnight Shift, 6p-6:30a)

Rentschler

Milford, MA • On-site

Full-time

Medical, Retirement

Re-posted 4 days ago

Job description

Advancing medicine to save lives. Together.
Thanks to many decades of experience and our passion for what we do, we make an essential contribution to the global availability of biopharmaceuticals, especially for patients with rare and serious diseases.
Rentschler Biopharma SE is a leading contract development and manufacturing organization (CDMO) focused exclusively on client projects. We offer customized full-service solutions for bioprocess development and the production of complex biopharmaceuticals. As a German family-owned company with an international footprint and global reach, we combine experts, expertise and years of experience to develop best-in-class solutions - together with our clients.
Rentschler Biopharma has approximately 1,400 employees and is headquartered in Laupheim, Germany, with a site in Milford, MA, USA. In 2024, we joined the United Nations Global Compact, underlining our commitment to sustainability.
As an independent family-owned company, we live by the motto: Many hands, many minds - ONE TEAM! Open, respectful cooperation characterizes our working environment, where quality awareness, diligence and responsibility are our top priorities. With all the diversity of our talents in the Rentschler team, we pursue one vision together: advancing medicine to save lives.
The Manufacturing Associate III is focused on biologics manufacturing, which includes processing in upstream (cell culture) and downstream (purification). Operators are expected to perform these processes while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which apply.
This position will follow an Overnight 4/3 schedule, 6pm-6:30am, Wed-Sat (working every other Wednesday).
Key Experience for Manufacturing Associate, Downstream
  • Experienced in GMP downstream manufacturing; especially with TFF, Chromatography systems and purification of Mabs
  • Specific equipment/systems that we are using include, Akta ready, Akta Process, XDUos buffer systems and disposable technology systems
  • Must have experience with troubleshooting of the equipment and of process and excellence in clinical manufacturing
  • Characteristics: adaptable to changes, works well cross functionally and with key stakeholders. self-motivated, takes initiative and drives for solutions with the team. Can lead in the absence of the manager. Could train newer operators once up to speed.
  • Other possible responsibilities may include writing deviations/investigations and revising batch records if needed.

Duties and Responsibilities
  • Perform operations of the following (may be applicable to commercial scale product, development studies, clinical scale or validation activities).
    • Strong knowledge and understanding of manufacturing process and equipment to perform various production steps.
    • Ability to train employees.
    • Subject matter expert operating production equipment, as needed.
    • Monitor and record batch parameters, including computer data entry. Complete relevant paperwork following GDP/GMP guidelines. Perform mathematical calculations related to production processes.
    • Initiate new documents for procedures; may make minor revisions to existing documents.
    • Work with support team on all necessary event investigations and inventory system cycle counts and discrepancies.
    • Troubleshoot process problems and respond to alarms. Provide information for unplanned events, including entering data into event management software.
    • Oversee training of new employees, track training requirements for team members ensuring appropriate training is completed prior to process execution.
    • Order, receive and distribute supplies into production area as needed.
    • Pushing buffer containers ranging from 50L to 200L.
    • Sitting for periods of 2 to 3 hours.
    • Knowledge of laboratory and pharmaceutical production equipment including but not limited to: autoclaves, process tanks, chromatography skids and columns, analytical equipment.
  • Convey information to external stake holders (auditors, global colleagues, etc.). Oversee support for groups that support manufacturing (such as external cleaners, etc.).
  • Lead Continuous Improvement Teams (such as 5S, Gemba, OMT, etc.).
  • Demonstrate procedures as a part of training sessions for other team members; may schedule department or process activities which could involve coworkers. Lead team meetings and facilitate multidepartment discussions.
  • Provide knowledge in areas of training process improvements
  • Such additional responsibilities as the Company may also assign.

Qualifications
  • With high school diploma: Normally requires 3-6 years of related experience required or an associate degree in Life Sciences/Engineering field. Biotech Certificate preferred
  • With Bachelor's degree: Normally requires 1-4 years of related experience
  • Demonstrated knowledge of CGMP manufacturing.
  • Knowledge of laboratory and pharmaceutical production equipment.
  • Able to read and follow detailed written instructions and have good verbal/written communication skills.
  • Able to write legibly and grammatically correct entries on records. Must be able to author technical procedures and create forms.
  • Familiar with standard troubleshooting approaches (problem statement, root cause analysis, corrections, etc.)
  • Good computer skills, knowledge of Microsoft Word, Excel.
  • Good interpersonal skills and be able to work effectively and efficiently in a team environment.
  • Ability to meet schedule required; this position may include shift, weekend, holiday work and overtime at times, as dictated by the 365-day per year production schedule.
  • Ability to work in a clean room environment and comply with hygiene standards and use of special garments. Additionally, personal protective equipment must be worn due to safety requirements.

Working Conditions
  • Normal office working conditions: computer, phone, files, fax, copier.
  • Personal Protective Equipment must be worn as required.
  • May require lifting amounts of 25 lbs.
  • Manufacturing operations tasks requires operator to regularly remain on feet for shift.

Physical Requirements
  • PPE as required.
  • May require lifting amounts of 25 lbs.
  • Manufacturing operations tasks requires operator to regularly remain on feet for shift.

Base Pay Range
$36/hr - $45/hr
Disclosure Statement
Rentschler Biopharma, Inc is committed to fair and equitable compensation practices. The base pay range listed for this position is the anticipated annual base salary range the organization reasonably, and in good faith, expects to pay for this position at this time. Actual compensation is determined based on several factors that may include seniority, education, training, relevant experience, relevant certifications, geography of work location, job responsibilities, or other application factors permissible by law. The annual base salary is just one component of our Total Rewards package, which also includes our annual discretionary bonus program, medical insurance, our generous 401K program, plus a host of other benefits to aligned to support our employees' personal and professional wellness. The salary pay range is subject to change and may be modified at any time.

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