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Biotech Process Development Jobs in Massachusetts

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Process Development Senior Scientist What you will do Let'sdo this.Let'schange the world. In this ...

Process Development Senior Scientist

Cambridge, MA · Hybrid

$100K - $136K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Process Development Senior Scientist What you will do Let's do this. Let's change the world. In ...

Process Development Senior Scientist

Cambridge, MA · On-site

$100K - $136K/yr

Career Category Process Development Join Amgen's Mission of Serving Patients At Amgen, if you feel ... Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ...

Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing, cell therapy products and process development * Ability to think critically, and demonstrated ...

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Biotech Process Development information

See Massachusetts salary details

$20

$34

$46

How much do biotech process development jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for biotech process development in Massachusetts is $34.37, according to ZipRecruiter salary data. Most workers in this role earn between $29.95 and $37.93 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 job categories do people searching Biotech Process Development jobs in Massachusetts look for? The top searched job categories for Biotech Process Development jobs in Massachusetts are:
What cities in Massachusetts are hiring for Biotech Process Development jobs? Cities in Massachusetts with the most Biotech Process Development job openings:
Senior Scientist, Analytical Development

Senior Scientist, Analytical Development

Aurion Biotech Inc.

Cambridge, MA

$155K - $170K/yr

Other

Medical, Retirement, PTO

Re-posted 2 days ago


Job description

Description

JOB TITLE: Senior Scientist, Analytical Development

LOCATION: Cambridge, MA

SALARY RANGE: $155,000 to $170,000


ABOUT THE POSITION

Aurion Biotech is seeking a highly motivated Senior Scientist, Analytical Development in Cambridge, MA. This position will serve as an integral part of a multidisciplinary team to develop, qualify, and transfer in-process control, characterization, and release assays to support early and late-stage clinical manufacturing and testing of cell therapy products. The individual in this role will work collaboratively with the Research, Process Development, Quality and other groups to make sure assays meet the timeline of characterization and release of cell therapy products.


KEY RESPONSIBILITIES

  • Conduct various independent laboratory experiments including but not limited to Flow Cytometry, cell counting, dPCR, qPCR, ELISA, cell-based potency assays etc. to satisfy the overall AD objectives.
  • Collaborate cross-functionally with other functions including Cell Production, Process Development, Manufacturing, and Quality. 
  • Author method qualification SOP, method qualification report and test method SOP and other technical documents to support regulatory submissions and other groups.
  • Track progress toward project milestones and ensure that deliverables are met.
  • Responsible for the development, optimization, qualification, and transfer of GMP-compliant analytical methods and materials that meet US FDA and/or EU regulatory requirements for clinical stage, cell therapy products.
  • Train other groups to execute various in-house assays. 
  • Experience with Quality Control and regulatory requirements for late-stage method development and documentation are highly preferred.
  • Other duties as assigned.


ABOUT AURION BIOTECH 

With offices in Seattle, Boston, and Tokyo, Aurion Biotech is a clinical-stage biotech company, whose mission is to restore vision to millions of patients with life-changing regenerative therapies. The Company's first candidate is for the treatment of corneal edema secondary to endothelial dysfunction, and one of the first clinically validated cell therapies for corneal care; it was recently granted regulatory approval from Japan's PMDA. Aurion Biotech is the recipient of the prestigious Prix Galien award for best start-up in biotech. The Company is preparing for clinical trials in the U.S. We are growing rapidly and seek to hire highly motivated candidates from diverse backgrounds, cultures, and experiences, who share our values:

  • Stewardship: We make the world a better place for our patients, our communities, our clinicians, and our colleagues. We act responsibly as individuals, as employees, and as a company. 
  • Transformation: We embrace our challenges, our successes, and our failures. We are curious, we take risks, and we collaborate. 
  • Grit: We break down walls and strive to achieve the impossible. We are persistent and resilient, and we deliver on our commitments.

Aurion Biotech has a lot to accomplish in the next few years, and this role is key to our success. Privately held, Aurion Biotech is backed by Alcon, the global leader in eye care. To learn more about Aurion Biotech, visit www.aurionbiotech.com


LIFE AT AURION BIOTECH

We want our people to wake up every morning excited and energized for work. We value employees, which is why we invest in making life at Aurion Biotech healthy, fun, and rewarding:

  • Robust Benefits: We offer full health insurance to employees and their families, and all the acronyms: 401(k) matching, EAP, FSA, and generous PTO.
  • Total Rewards: We offer competitive compensation packages to ensure all Aurion employees are rewarded for their hard work.
  • Perks and Fun: Paid parking, subsidized commuter passes, in-office catered lunches, team events, and community projects are just a few ways that we bond, celebrate each other, have fun, and live our values.

Requirements

QUALIFICATIONS AND EDUCATION

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the education, experience, knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • A PhD and 3-5 years' experience or an MS degree and 6-8 years of experience in a relevant discipline (immunology, biochemistry, cell biology, biotechnology, or related field) in the pharmaceutical industry and academia, and specifically in gene and cell therapy.
  • Experience with biological therapeutic products is critical, experience specifically with cell therapy technologies is preferred.
  • Demonstrated track record with analytical development supporting early and late-stage development of cell therapies.
  • Deep technical understanding of analytical method development for key assays (Flow Cytometry, automated cell counting, dPCR, qPCR, ELISA, cell-based potency) and associated requirements (validation, stability programs, comparability assessments, etc.) across development is required.

REQUIRED SKILLS, KNOWLEDGE, AND ABILITIES

  • The ability to work in a dynamic, fast-paced, matrix environment, manage priorities and maintain timelines for multiple projects.
  • Demonstrated ability to technically trouble shoot and resolve assay challenges to successfully produce cell therapy products at a high-performance rate.
  • Demonstrated ability to develop, qualify/validate and transfer biologics analytics into manufacturing processes and product testing that meet customer needs is required.
  • The ability to work both independently and in a matrix team environment is essential.
  • Must have strong interpersonal and communication skills, be a team player and be willing to work in an environment where individual initiative, accountability to the team, and professional maturity are required.
  • Knowledge of Manufacturing to develop and innovate next-generation analytical tools for characterization.
  • Familiar with data analytics software such as FlowJo, JMP, and GraphPad Prism.