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Biotech Manufacturing Associate Jobs in Massachusetts

Sanofi EU

Senior Manufacturing Technician

Lynn, 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

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

$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

$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 ...

Lonza

Associate Director Business Development

Boston, MA · On-site

$150K - $200K/yr

... Manufacturing, and Drug Product capabilities. This role will be responsible for developing ... Identify, engage, and acquire new customer relationships within biotechnology and pharmaceutical ...

Lonza

Associate Director Business Development

Boston, MA · On-site +1

$150K - $200K/yr

... Manufacturing, and Drug Product capabilities. This role will be responsible for developing ... Identify, engage, and acquire new customer relationships within biotechnology and pharmaceutical ...

Sanofi EU

Sr Manufacturing Technician

Boston, MA

$24 - $32/hr

The Sr. Manufacturing Technician will be responsible for performing a variety of complex tasks ... Biotech Certificate or Associate's degree in a related field with 6 months of experience (including ...

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Biotech Manufacturing Associate information

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$13

$22

$36

How much do biotech manufacturing associate jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for biotech manufacturing associate in Massachusetts is $22.76, according to ZipRecruiter salary data. Most workers in this role earn between $17.84 and $25.48 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 Massachusetts?

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

What job categories do people searching Biotech Manufacturing Associate jobs in Massachusetts look for?

The top searched job categories for Biotech Manufacturing Associate jobs in Massachusetts are:

What cities in Massachusetts are hiring for Biotech Manufacturing Associate jobs?

Cities in Massachusetts with the most Biotech Manufacturing Associate job openings:

Biotech Manufacturing Associate jobs near you
Infographic showing various Biotech Manufacturing Associate job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 66% Full Time, 28% Part Time, 2% Temporary, 2% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $47,334 per year, or $22.8 per hour.

CMC Project Leader

HONGENE BIOTECH CORPORATION

Cambridge, MA • On-site

$140K - $190K/yr

Full-time

Re-posted 21 days ago

Job description

Job Title

Associate Director / Senior Manager, CMC Project Management

Location

Boston area preferred (or ability to commute regularly)

Company Overview

Hongene Biotech is a global leader in nucleic acid manufacturing, supporting RNA therapeutics, mRNA vaccines, and molecular diagnostics. With a vertically integrated platform from raw materials to CDMO services, we enable our partners to accelerate development with efficiency and quality.

Position Overview

This role will report directly to the VP, Global Head of CMC & Regulatory and is critical in strengthening Hongene’s project management capabilities for its oligonucleotide contract manufacturing services.

Level and title will be determined based on experience. We are primarily targeting Senior Manager to Associate Director level. Exceptional candidates may be considered at Director level.

The Primary Job Responsibilities

1) Drive project management efforts associated with CMC activities to support oligonucleotide contract manufacturing projects at Hongene Biotech.

2) Support Head of CMC and Oligonucleotide team in developing and executing development and manufacturing strategy and tactical executional plans.

3) Bridge communication between Clients and the internal teams in support of multiple contract manufacturing projects for different clients, including participation in technical calls, tracking of action items and facilitating rapid decision making within the team to drive programs forward.

4) Coordination with AD/PD, manufacture, quality and BD team to build, and manage global clients’ project timelines, work with BD to generating RFP proposals and evaluate necessary resources and ensure RFP proposals are aligned with overall strategy and cost estimation. Proactively identify potential risks, resourcing constraints and conflicts that could impact project timelines; collaborate with the AD/PD, manufacturing, QA/QC teams to develop appropriate solutions.

5) Support projects with strategic partners in US.

The candidate must have strong communication skills and be capable of strategically communicating with internal and external stakeholders, as well as effectively communicating across functions and fluent speaking both English and Mandarin. Finally, the candidate must be comfortable with, and thrive in, a fast-paced entrepreneurial environment.

Minimal Requirements

• B.S or M.S in Pharmaceutical Science, Chemistry, Biochemistry, or related scientific discipline with 8+ years of applicable experience in the biotechnology or pharmaceutical industry.

• Demonstrated proficiency in the discipline of project management. Experience with operating in a GMP environment and working in cross functional environments. Demonstrated ability to exercise independent judgement and strategic thinking.

• Strong interpersonal skills and experience of managing cross-function projects.

• Ability to thrive in a fast-paced, hands-on research and development environment.

• Adept at building strong relationships and collaborating with colleagues at all levels.

• Ability to discern paths forward within ambiguous environments.

• Excellent verbal, written, and presentation skills for communication with internal and external customers is essential.

Preferred Qualifications

• Minimum of 5 years’ experience in project or program management at a biotechnology or pharmaceutical company with direct involvement in the CMC area

• Experience with project management tools (e.g. MS Project, Smartsheet, Clarizen) and collaboration tools (BOX, SharePoint, MS Teams)

• Understanding of the different phases of drug development and cGMP requirements

• Experience in small molecules, oligonucleotides, or biologic drug development

• Located in US EST time zone