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Msat Process Development Scientist Jobs (NOW HIRING)

Lonza

MSAT Process Scientist/Engineer II

Portsmouth, NH · On-site

MSAT Process Scientist/Engineer II Location : On-site, Portsmouth, NH. Relocation assistance is ... This person has developed a core competency in transferring and supporting processes from first run ...

Lonza

MSAT Process Scientist/Engineer II

Portsmouth, NH · On-site

MSAT Process Scientist/Engineer II Location : On-site, Portsmouth, NH. Relocation assistance is ... This person has developed a core competency in transferring and supporting processes from first run ...

Cascade Bio

Process Development Scientist

Denver, CO · On-site

$110K - $150K/yr

Process Development Scientist Location: Denver, CO (on-site) Type: Full-time Cascade Biocatalysts is building the next generation of industrial biocatalysts and is seeking a hands-on Process ...

Cascade Bio

Process Development Scientist

Denver, CO · On-site

$110K - $150K/yr

Process Development Scientist Location: Denver, CO (on-site) Type: Full-time Cascade Biocatalysts is building the next generation of industrial biocatalysts and is seeking a hands-on Process ...

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How much do msat process development scientist jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for msat process development scientist in the United States is $38.66, according to ZipRecruiter salary data. Most workers in this role earn between $28.37 and $46.15 per hour, depending on experience, location, and employer.

What does a MSAT Process Development Scientist do?

A MSAT (Manufacturing Science and Technology) Process Development Scientist is responsible for developing, optimizing, and transferring manufacturing processes in the biotechnology or pharmaceutical industry. They work to ensure that production methods are efficient, reproducible, and compliant with regulatory standards. Their role often bridges the gap between research and large-scale manufacturing, troubleshooting technical issues and implementing process improvements to ensure product quality and consistency.

What are the key skills and qualifications needed to thrive as an MSAT Process Development Scientist?

To thrive as an MSAT Process Development Scientist, you need a strong background in bioprocess engineering, chemistry, or related fields, typically supported by a relevant degree and experience in biologics manufacturing. Familiarity with process analytical technology (PAT), statistical analysis software, and quality systems such as GMP is essential. Strong problem-solving, communication, and teamwork skills set individuals apart in this role. These competencies ensure effective process optimization, regulatory compliance, and successful technology transfer in biopharmaceutical production.

What are some common challenges faced by MSAT Process Development Scientists when scaling up processes from the lab to manufacturing?

MSAT Process Development Scientists often encounter challenges such as ensuring process consistency, managing variations in raw materials, and addressing equipment limitations when scaling up from lab to manufacturing scale. Differences in mixing, temperature control, and reaction times can lead to unexpected outcomes that require troubleshooting and adaptation of protocols. Collaborating closely with manufacturing, quality, and engineering teams is essential to identify and resolve these issues efficiently, ensuring a smooth transfer and robust commercial production.

What is the difference between Msat Process Development Scientist vs Process Development Scientist?

AspectMsat Process Development ScientistProcess Development Scientist
Required CredentialsBachelor's or Master's in Life Sciences, Chemistry, or related field; experience with cell therapy or biologics manufacturingBachelor's or Master's in similar fields; often includes experience in biologics or pharmaceutical process development
Work EnvironmentLaboratory and manufacturing settings focused on cell therapy processesLaboratory and pilot plant environments for biologics or pharmaceutical processes
Employer & Industry UsageBiotech and cell therapy companiesPharmaceutical and biotech industries

The Msat Process Development Scientist specializes in developing and optimizing manufacturing processes for cell therapy products, often working closely with manufacturing teams. In contrast, the Process Development Scientist has a broader focus on biologics or pharmaceutical processes. Both roles require similar educational backgrounds and work environments, but their specific industry applications and product focus differ.

What are popular job titles related to Msat Process Development Scientist jobs?

For Msat Process Development Scientist jobs, the most frequently searched job titles are:

Infographic showing various Msat Process Development Scientist job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $80,420 per year, or $38.7 per hour.

MSAT Process Development Engineering Scientist (Contract)

Boston, MA • On-site

Vertex Pharmaceuticals Incorporated
Biotechnology Research and Development • 1 - 5K employees
Learn more about Vertex Pharmaceuticals Incorporatedexternal

$60 - $67/hr

Other

Re-posted 22 days ago

Vertex Pharmaceuticals rating

6.5

Company rating: 6.5 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

Job description


Process Development Engineering Scientist
Vertex, a biopharmaceutical company focused on developing a cell and gene-based therapies for multiple indications, is seeking a Process Development Engineering Scientist to join our Process Development - Technical Sciences group in Boston, MA.
The successful candidate will be responsible for Manufacturing Science and Technology (MSAT) activities for cell therapy products in our Type 1 Diabetes (T1D) program and Casgevy program. The candidate will provide cross-functional leadership in technology development and transfer from Development to Clinical Manufacturing and Process Performance Qualification including internal operations and potentially various CDMOs. The candidate will also plan and implement continuous improvement initiatives for life-cycle management working in cross-functional environment.
This role is onsite.
6 month contract with chance to extend.
Responsibilities:
  • Lead triage, investigation, and change control implementation as a Manufacturing Science and Technology functional area assessor and identify improvements, implement changes, and monitor clinical and commercial manufacturing processes.
  • Manage the execution of deliverables, both short and long-term, via clearly defined milestones, and timelines. Minimize timeline deviations by clearly identifying program risks and communication of strategies
  • Review and contribute to regulatory submissions (IND, IMPD). Author supporting documents and reports.
  • Coordinate and integrate cross-functional activities to ensure alignment in scope, schedule and budget
  • Drive continuous improvement activities and operational excellence, including COGS reduction and commercial readiness.
  • Champion pre-PPQ and PPQ activities.
  • Establish robust process performance across all clinical and commercial manufacturing lines, including process development, process improvement, and maintenance of process excellence. Lead process monitoring, continuous improvement, and lifecycle management initiatives guided by risk assessment and mitigation strategies
  • Oversee CDMOs activities by providing guidance and support in collaborative manner. Be responsible for the performance, quality and delivery of external collaborators
  • Collaborate within departmental teams, actively contribute to deliverables and engage in team discussion on issue resolution.

Preferred qualifications:
  • PhD in Life Sciences, chemical engineering, or related discipline or Master's degree with minimum 3+ years of industry experience or Bachelor's degree with 6+ years of relevant industry experience.
  • Hands on experience with Manufacturing Science and Technology (MSAT) investigation and change management. Experience with cell-gene therapy is preferred.
  • Hands on experience with regulatory filings is preferred.
  • Experience working with cell processing, specifically with primary cells. Experience with cell therapy products is preferred
  • Knowledge of cGXP theory and practices is required.
  • Ability to communicate effectively with a diverse range of scientists, engineers, regulatory specialists, and business professionals
  • Proven experience with MSAT, Process Technology Transfer, Technical Operations, and Lifecycle Management.
  • Knowledge of Design Control and Risk Management, including experience using FMEA analyses.
  • Must be able to work independently with adequate supervision and support in parallel a few projects.
  • Must demonstrate strong interpersonal and teamwork skills, with experience managing and training team.

Pay Range
$60-$67/HR
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
By applying for this position, you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials, which may include your CV/Resume, email address or phone number, with Vertex. For more information on how Vertex handles your personal data related to your job application, please see Vertex's Careers Privacy Notice. Agreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners
(collectively, "Atrium Alerts"). Atrium Alerts may be sent by email, phone, or text message. Your personal information will be safely stored within the Atrium & Vertex databases. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time, please contact Atrium at privacyadministrator@atriumstaff.com.
If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.
No C2C or Third-Party Vendors

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