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Biotech Process Development Jobs in Boston, MA (NOW HIRING)

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Biotech Process Development information

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How much do biotech process development jobs pay per hour?

As of Jun 29, 2026, the average hourly pay for biotech process development in Boston, MA is $36.59, according to ZipRecruiter salary data. Most workers in this role earn between $30.05 and $44.90 per hour, depending on experience, location, and employer.

What is biotech process development?

Biotech process development refers to the design, optimization, and scale-up of manufacturing processes used to produce biological products, such as pharmaceuticals, enzymes, or vaccines. Professionals in this field work to turn laboratory procedures into efficient, large-scale industrial processes that meet regulatory and quality standards. This often involves selecting suitable equipment, optimizing conditions, ensuring reproducibility, and troubleshooting production issues. The ultimate goal is to produce high-quality products safely, consistently, and cost-effectively.

What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?

AspectBiotech Process DevelopmentBiotech Manufacturing Associate
Primary FocusDesigning, optimizing, and scaling up bioprocesses for product developmentExecuting manufacturing processes to produce biopharmaceuticals at scale
Work EnvironmentLaboratories and pilot plant facilitiesProduction floors and manufacturing plants
Required SkillsProcess design, lab techniques, troubleshootingEquipment operation, quality control, adherence to SOPs
Typical CredentialsBSc/MSc in Biotechnology, Chemical Engineering, or related fieldsBSc in Biotechnology, Biology, or related fields

While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.

What are the key skills and qualifications needed to thrive in Biotech Process Development, and why are they important?

To excel in Biotech Process Development, you need a strong background in bioprocess engineering, molecular biology, and chemistry, typically supported by a degree in biotechnology or related fields. Familiarity with tools such as bioreactors, chromatography systems, and data analysis software, along with certifications in Good Manufacturing Practice (GMP), is highly valuable. Strong problem-solving skills, attention to detail, and effective teamwork distinguish top performers in this role. These competencies are crucial for optimizing processes, ensuring product quality, and driving innovation in the biotech industry.

What are some common challenges faced by professionals in Biotech Process Development, and how are they typically addressed?

Professionals in Biotech Process Development often encounter challenges related to scaling up processes from the laboratory to commercial production, ensuring product consistency, and meeting strict regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing. Continuous process optimization, thorough documentation, and robust validation protocols are essential strategies to overcome these hurdles and ensure successful product development and commercialization.
What are popular job titles related to Biotech Process Development jobs in Boston, MA? For Biotech Process Development jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Biotech Process Development jobs in Boston, MA look for? The top searched job categories for Biotech Process Development jobs in Boston, MA are:
What cities near Boston, MA are hiring for Biotech Process Development jobs? Cities near Boston, MA with the most Biotech Process Development job openings:
Associate Engineer, Drug Development Process Improvement (JP13693)

Associate Engineer, Drug Development Process Improvement (JP13693)

3 Key Consulting

Cambridge, MA • Hybrid

$30 - $35/hr

Other

Posted 9 days ago


Job description

Job Title: Associate Engineer, Drug Development Process Improvement (JP13693)
Location: Cambridge, MA. 02138
Business Unit: DST Synthetics B
Employment Type: Contract
Duration: 2+ year with likely extensions and/or conversion to a permanent position.
Rate: $30 - $35/hour W2
Posting Date: 02/25/2025.
Notes: Only qualified candidates need apply.
3 Key Consulting is hiring! We are recruiting an Engineer for a consulting engagement with our direct client, a leading global biotechnology company.
Job Description:
As the DST representative you will be responsible to collaborate with the product delivery team(s) to work with the manufacturing organization(s) to ensure drug substance supply and resolve challenges, identifying and implementing process improvements, and authoring regulatory documents in support of the product lifecycle works with a multi-functional group of engineers and scientists through the process development cycle at client to ensure our process requirements and knowledge are suitable for its intended phase of technology transfer: process introduction, clinical manufacturing, validation and commercial manufacturing. Partners with our manufacturing teams to assess the equipment and manufacturing operations meet process requirements, where necessary work with the sites(s) to introduce processes that deliver meaningful therapeutics for our patients.
Top Must Have Skill Sets:
Academic background in Chemical Engineering with strong knowledge in engineering principles and/or organic chemistry with basic understanding of cGMP/GLP requirements.
Knowledge of analytical techniques and solid-state characterization and familiarity with statistical analysis and working knowledge of standard plant operations and safety practices
Excellent project management skills, Strong verbal communication and presentation skills
Willing to be hybrid as needed.
Day to Day Responsibilities:
Critically evaluate new processes for identification of process improvements and requirements necessary to prepare processes for scale up and tech transfer.
Use, refine and develop models for reaction kinetics, mass transfer, separations, distillations, isolations, drying, and relevant hydrodynamic operations.
Analyze and document the economic value of existing, proposed process solutions and new process concepts.
Apply standard engineering techniques and procedures to provide solutions to a variety of technical chemical and process issues that will be encountered during process development, tech transfer and scale-up.
Routinely monitor manufacturing processes for performance indicators and operations.
Apply engineering principles and statistical analysis, including design of experiments, in-order to critically evaluate chemical processes for identification of process improvements and requirements necessary for scale up and tech transfer.
Author, review and/or approve of process documentation needed for process validation and commercialization.
Provide support to commercial projects to support supply demand, ensure highest quality standards and guarantee patient safety.
Work closely with process development chemists, formulation scientists and analytical chemists to generate and interpret data to provide improved understanding and guidance for synthesis, unit operations and life cycle phase of commercial products.
Basic Qualifications:
Bachelor degree OR Associate degree and 4 years of experience OR High school diploma / GED and 6 years of experience
Why is the Position Open?
Backfill
Interview Process:
Phone Screen followed by Phone interview
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.