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Process Development Associate Jobs in Canton, MA

Development Associate

Boston, MA · On-site

$50K - $65K/yr

Additionally, they will be a team player, exceptionally detail-oriented and organized, process-driven, and a superb writer. The Development Associate will report to the Director of Development and ...

Development Associate

Boston, MA · On-site

$50K - $65K/yr

Additionally, they will be a team player, exceptionally detail-oriented and organized, process-driven, and a superb writer. The Development Associate will report to the Director of Development and ...

Additionally, they will be a team player, exceptionally detail-oriented and organized, process-driven, and a superb writer. The Development Associate will report to the Director of Development and ...

The Development Associate works closely with the SAVP, an Executive Director of Advancement who ... Prepare gift documentation, review and process expense reports for SAVP approval, and reconcile ...

Development Associate

Boston, MA · On-site

$40K - $45K/yr

Development Associate, Best Buddies Challenges Department : Strategic Development and Marketing ... Create and follow participant on-boarding, lead-flow, and fundraising stratification processes and ...

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Process Development Associate information

See Canton, MA salary details

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$35

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How much do process development associate jobs pay per hour?

As of Jun 20, 2026, the average hourly pay for process development associate in Canton, MA is $35.62, according to ZipRecruiter salary data. Most workers in this role earn between $29.23 and $43.70 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 job categories do people searching Process Development Associate jobs in Canton, MA look for? The top searched job categories for Process Development Associate jobs in Canton, MA are:
What cities near Canton, MA are hiring for Process Development Associate jobs? Cities near Canton, MA with the most Process Development Associate job openings:
Process Development Sr. Scientific Associate (Contract)

Process Development Sr. Scientific Associate (Contract)

Vertex Pharmaceuticals Incorporated

Boston, MA • On-site

$38/hr

Full-time

Posted 9 days ago


Job description

Job Description
The Process Dev Engineering Senior Research Associate will be part of a team responsible for process development and optimization, as well as characterization of cell product for ongoing and future projects.
Key Duties and Responsibilities:
  • Participates in the design and planning of process development and process characterization studies under the supervision of senior members.
  • Maintains 2D and 3D pluripotent stem cell culture in various cell culture platforms.
  • Formulate media and factors according to established procedures.
  • Documents experimental procedures, observation, and results in electronic lab notebook.
  • Compile study raw data in various formats and conducts basic data analysis.
  • Supports a fully integrated team to facilitate the success of projects.
  • Works within departmental teams, supports deliverables and participates in team discussion on issue resolution.

Knowledge and Skills:
  • Experience with cell culture and aseptic technique. Bioreactor operation experience preferred.
  • Good communication skills to share technical/scientific information within the team.
  • Willingness to learn and take initiatives, with a team-oriented attitude.
  • Ability to follow detailed instructions and to maintain detailed and accurate records and notes.
  • Must be skilled in the Windows operating system and Microsoft Office, including Word, Excel and PowerPoint. JMP and GraphPad Prism preferred.
  • Work weekends (Saturday and Sunday) are required and have a flexible schedule to work some holidays

Education and Experience:
  • >2 year experience, Bachelor's degree in Biology, Biochemical engineering, or a related discipline is required

Contract length: 6 months with the chance to extend.
Pay Range
$38/hr. - $40/hr.
Shift/Hours
Monday - Friday
Requisition Disclaimer
This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals ("Vertex"). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements
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