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Process Development Associate Jobs in Boston, MA

Amgen

Process Development Senior Associate

Cambridge, MA · On-site +1

$85K - $103K/yr

Process Development Senior Associate Duties: Conduct experiments, analyze results, and implement process improvements to enhance efficiency and product quality; Design, develop, and optimize ...

DigitalOcean

Corporate Development Associate

Boston, MA · Remote

$110K - $134K/yr

We are looking for a Corporate Development Associate who is passionate about driving impactful ... in due diligence processes, analyzing financial, legal, and operational data * Support the ...

NorthEastern

Research Development Associate

Boston, MA · On-site

About the Opportunity Job Summary The Research Development (RD) Associate is responsible for the ... This includes scheduling, communications, documentation and reporting, process improvements, and ...

Partners Capital

Business Development Associate

Boston, MA · On-site

$48K - $66K/yr

The Associate will work closely with Business Development and Investment team members to support ... Manage internal deadlines for those involved in the process * Liaise with internal teams (i.e ...

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How much do process development associate jobs pay per hour?

As of Jun 5, 2026, the average hourly pay for process development associate in Boston, MA is $36.64, according to ZipRecruiter salary data. Most workers in this role earn between $30.05 and $44.95 per hour, depending on experience, location, and employer.

What is the difference between Process Development Associate vs Process Engineer?

AspectProcess Development AssociateProcess Engineer
Required CredentialsBachelor's in Chemistry, Chemical Engineering, or related field; often some experience in process developmentBachelor's or Master's in Chemical Engineering or related; more emphasis on engineering principles
Work EnvironmentLaboratory and pilot plant settings, focused on process research and developmentManufacturing plants, production lines, and process optimization environments
Employer & Industry UsagePharmaceutical, biotech, and chemical industries; entry to mid-level rolesChemical, manufacturing, and process industries; more senior roles in process optimization

The Process Development Associate primarily focuses on developing and optimizing new processes in lab and pilot settings, often working closely with R&D teams. In contrast, the Process Engineer applies engineering principles to scale up processes, improve manufacturing efficiency, and troubleshoot production issues. While both roles require a background in chemical or process engineering, the Process Development Associate is more research-oriented, whereas the Process Engineer emphasizes process implementation and optimization in production environments.

What are the key skills and qualifications needed to thrive as a Process Development Associate, and why are they important?

To thrive as a Process Development Associate, you need a strong background in biochemistry, chemical engineering, or a related field, often supported by a bachelor’s or master’s degree. Experience with laboratory instrumentation, process optimization tools, and familiarity with regulatory standards such as GMP are typically required. Attention to detail, problem-solving abilities, and effective teamwork are vital soft skills for excelling in this role. These competencies are crucial for ensuring efficient process design, regulatory compliance, and successful scale-up in manufacturing environments.

What is a Process Development Associate?

A Process Development Associate is a professional who assists in designing, optimizing, and scaling up manufacturing processes, typically in industries such as biotechnology, pharmaceuticals, or chemical engineering. They work closely with scientists and engineers to develop efficient, safe, and cost-effective processes for producing products or materials. Their responsibilities often include conducting experiments, collecting and analyzing data, troubleshooting process issues, and supporting technology transfer to manufacturing. This role is essential for ensuring that new or improved products can be produced reliably at larger scales. Process Development Associates help bridge the gap between research and full-scale production.

What are the primary challenges faced by a Process Development Associate when scaling up laboratory processes to manufacturing scale?

A Process Development Associate often encounters challenges in translating small-scale laboratory protocols into large-scale manufacturing processes. Variations in equipment, raw material quality, and environmental conditions can impact reproducibility and efficiency. Addressing these issues requires strong troubleshooting skills, attention to detail, and close collaboration with cross-functional teams such as manufacturing, quality assurance, and engineering to ensure smooth technology transfer and consistent product quality.
What are the most commonly searched types of Process Development jobs in Boston, MA? The most popular types of Process Development jobs in Boston, MA are:
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What job categories do people searching Process Development Associate jobs in Boston, MA look for? The top searched job categories for Process Development Associate jobs in Boston, MA are:
What cities near Boston, MA are hiring for Process Development Associate jobs? Cities near Boston, MA with the most Process Development Associate job openings:
Process Development Associate jobs near you
Infographic showing various Process Development Associate job openings in Boston, MA as of May 2026, with employment types broken down into 88% Full Time, 4% Part Time, and 8% Contract. Highlights an 81% In-person, 15% Hybrid, and 4% Remote job distribution, with an average salary of $76,207 per year, or $36.6 per hour.
Late-Stage LNP Process Development Scientist

Late-Stage LNP Process Development Scientist

Eurofins

Boston, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago

Eurofins rating

7.5

Company rating: 7.5 out of 10

Based on 174 frontline employees who took The Breakroom Quiz

56th of 103 rated laboratories

Job description

Company Description
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you're looking for a rewarding career, a place to call home, apply with us today!
Job Description
As a member of the Late-Stage LNP Process Development team, the candidate will be joining a team conducting laboratory studies to support the process development, process scale-up, and process characterization of LNP clinical stage drug products. The successful candidate will have experience with LNP process development (having additional experience in tech transfer and GMP manufacturing is a plus but not required), and a desire to contribute to a team focused on establishing science-based manufacturing solutions for complex nucleic acid-based drug products. In this highly collaborative and cross-functional role, the candidate will support the refinement of process control and improve process understanding for multiple programs at various stages of clinical development.
  • Support routine process development and process characterization activities centered around the LNP drug product manufacturing process. Batch ranges vary from 10 mg to 1 gram.
  • Execute routine analytics including dynamic light scattering (DLS), UV-quantification via Ribogreen®, pH, and osmolality for in-process monitoring.
  • Perform experiments under limited to no supervision under subject matter expert guidance.
  • Organize and analyze data, interpret results, and present findings within the process development team and cross-functionally.
  • Author technical documentation (SOPs, reports, protocols) as required.
  • Document experiments and protocols using electronic lab notebooks (e.g., Benchling).
  • Maintain laboratory equipment, order critical reagents, and support operational excellence activities.

Qualifications
Minimum Required Qualifications:
  • B.S. degree in chemical/biomedical engineering, chemistry, or biological sciences (or related field) with 3-4 years of relevant laboratory experience. M.S. degree in biological or biochemical sciences (or related field) with 1-2 years of relevant laboratory experience.
  • Proficiency in bench-scale drug product manufacturing of LNPs with a focus on mixing and tangential flow filtration (TFF) processes.
  • Experience with practices and equipment used in process development of nucleic acids (experience with T-mixing and TFF is preferred).
  • Experience with DLS and osmolality for in-process monitoring.
  • Experience working with ELN systems such as Benchling.
  • Experience with technical documentation (SOPs, technical reports, protocols).
  • Ability to follow established SOPs for routine analytics.
  • Ability to achieve results, keep to a timeline, and find solutions to ensure that overall project deliverables are met.
  • Strong attention to detail, analysis of data/reports, troubleshooting, and problem-solving abilities.
  • Strong writing and communication skills with the ability to understand and communicate scientific information.
  • Strong organizational and time management skills.
  • Willingness to collaborate with cross-functional teams.
  • Proactive, creative, and positive attitude.

Preferred Qualifications:
  • Experience with UV-quantification via Ribogreen®.
  • Experience with GMP manufacturing practices and tech transfer operations is a plus.
  • Experience with statistical analysis software (i.e. JMP, Design Expert, etc.) is a plus.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.

Additional Information
The position is full-time, Monday-Friday, 8am-5pm with overtime as needed. Candidates living within a commutable distance of Boston, MA are encouraged to apply.
Excellent full-time benefits include:
  • Comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
  • Eligibility for yearly goal-based bonus & merit-based increases
  • Compensation: $36.00-$42.00 per hour

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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