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Cell Therapy Process Development Jobs in Lexington, MA

RoslinCT US

Senior Process Engineer

Hopkinton, MA

$114K - $147K/yr

WHO WE ARE We are a leading cell therapy contract development and manufacturing organization ... The Process Engineer will play a key role in optimizing manufacturing processes, ensuring ...

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Cell Therapy Process Development information

See Lexington, MA salary details

$21

$37

$55

How much do cell therapy process development jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for cell therapy process development in Lexington, MA is $37.84, according to ZipRecruiter salary data. Most workers in this role earn between $31.06 and $46.44 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a cell therapy process development professional?

To thrive in Cell Therapy Process Development, you need a solid background in cell biology, biotechnology, or a related field, often supported by a relevant degree and experience with cell culture techniques. Familiarity with bioprocessing equipment, Good Manufacturing Practice (GMP) regulations, and analytical tools such as flow cytometry and PCR is typically required. Strong problem-solving skills, attention to detail, and effective teamwork enhance performance in this collaborative and innovative environment. These competencies ensure the safe and efficient development of cell therapies, meeting rigorous quality standards and advancing clinical applications.

What are some typical challenges faced by professionals in cell therapy process development, and how are they addressed?

Professionals in Cell Therapy Process Development often encounter challenges such as scaling up production processes from laboratory to clinical or commercial scale while maintaining product quality and consistency. Additional hurdles include adhering to strict regulatory requirements and managing complex collaborations across cross-functional teams, like quality assurance, regulatory affairs, and manufacturing. These challenges are typically addressed through rigorous process optimization, thorough documentation, and ongoing communication with stakeholders to ensure that all aspects of the process meet industry standards and regulatory expectations.

What is the difference between Cell Therapy Process Development vs Cell Therapy Manufacturing Specialist?

AspectCell Therapy Process DevelopmentCell Therapy Manufacturing Specialist
CredentialsTypically requires a degree in biology, biochemistry, or biomedical engineering; certifications in GMP or cell therapy are commonSimilar credentials; often holds degrees in related fields and GMP certifications
Work EnvironmentResearch labs, development facilities, early-stage process optimizationManufacturing plants, production floors, quality control labs
Industry UsageFocuses on developing and optimizing cell therapy processesInvolved in large-scale production and process execution

Cell Therapy Process Development professionals focus on designing and refining cell therapy procedures, while Cell Therapy Manufacturing Specialists handle the production and quality assurance in manufacturing settings. Both roles require similar educational backgrounds and certifications but differ mainly in their work environment and specific responsibilities.

What is cell therapy process development?

Cell Therapy Process Development refers to the design, optimization, and scaling up of manufacturing processes for cell-based therapies, such as CAR-T cells or stem cell products. Professionals in this field work on translating laboratory research into reproducible, efficient, and safe production methods that meet regulatory standards. This involves working with cell culture techniques, bioreactors, quality control, and process validation to ensure that therapies can be produced consistently for clinical and commercial use. The goal is to develop robust processes that deliver safe and effective cell therapies to patients.
What are popular job titles related to Cell Therapy Process Development jobs in Lexington, MA? For Cell Therapy Process Development jobs in Lexington, MA, the most frequently searched job titles are:
What job categories do people searching Cell Therapy Process Development jobs in Lexington, MA look for? The top searched job categories for Cell Therapy Process Development jobs in Lexington, MA are:
What cities near Lexington, MA are hiring for Cell Therapy Process Development jobs? Cities near Lexington, MA with the most Cell Therapy Process Development job openings:
Cell Therapy Process Development jobs near you
Infographic showing various Cell Therapy Process Development job openings in Lexington, MA as of August 2026, with employment types broken down into 70% Full Time, and 30% Part Time. Highlights an 100% In-person job distribution, with an average salary of $78,716 per year, or $37.8 per hour.

Associate Director, Cell Therapy Territory Operations Manager

AstraZeneca GmbH

Boston, MA • On-site

$150 - $225/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 4 days ago

Job description

In AstraZeneca's Cell Therapy division, we follow the science to explore and innovate. We are working towards treating, preventing, modifying, and even curing some of the world's most complex diseases. We have the potential to grow our pipeline and positively impact the lives of patients around the world. We are committed to making a difference and have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs.

The Associate Director – Territory Operations Manager (AD-TOM) is a regional expert supporting Patient Operations and project teams in cell therapy. As a senior technical leader, the role sets and implements compliant policies and standards for treatment centers, partners with Regional Operations Directors (RODs) on site strategy, leads research and internal reporting, and maintains up-to-date best practices.

The role expands AZ’s cell therapy footprint in oncology by building patient-centered service lines and leading complex engagements with site leadership and frontline providers. It delivers operational and clinical guidance for trials and commercial products, leads site activation, and provides ongoing operational, quality, and clinical oversight post-activation.The AD-TOM is a field, regional role supporting the Northern Atlantic territory (with preference for candidate to be based in Massachusetts) and will report to a Regional Operations Director (ROD).

You Will:

  • Lead and support strategic initiatives across clinical and commercial cell therapy from development to post-market.

  • Be a key leader within Internal AZ teams (Program Management, QA, Manufacturing, Supply Chain, Medical Affairs, Market Access, Compliance, Sales/Marketing).

  • Establish service lines with external partners (PIs, Physicians, Nursing, Apheresis, Cell Therapy Lab, other HCPs/leadership).

  • Serve as SME, driving decisions and projects at multi-country/local levels; influence strategy, governance, and cross-functional execution.

  • Acts as the technical expert and authoritative source of knowledge in cell therapy workflows and brings expertise to site interactions.

  • Build and maintain relationships with stakeholders at assigned Sites.

  • Operate within regulatory/accreditation standards (e.g., FACT) ensuring compliance, audit readiness, and continuous improvement.

  • Guide clinical workflows; ensure standards; advance apheresis excellence; optimize product handling; inform health outcomes.

  • Act as primary operations readiness liaison; collaborate with Supply Chain to align logistics and site needs.

  • Provide exemplary customer service while building business relations with clinical/operational leaders.

  • Lead cross-functional meetings to develop product/patient workflows for trials and future commercial products.

  • Maintain strong collaboration with Program Management, SMM, Supply Chain, Manufacturing, Quality, Medical, Commercial, Cell Therapy Hub, to manage customer centers and clinical care for the portfolio.

  • Oversee operational/clinical aspects of raw material collection, product receipt/storage/distribution/infusion, and COI/COC.

  • Design and deliver training to PIs, MD, Nursing Staff, Apheresis, and Cell Therapy Laboratory and Coordinator staff

  • Lead Site activation using risk-based tools for certification, training, and monitoring.

  • Train Site HCPs on product needs; ensure COI/COC access for trained individuals with Cell Therapy Hub.

  • Oversee Site logistics and manage regional account changes with Cell Therapy Hub.

  • Respond to SOP deviations with expertise and collegiality.

  • Support/own quality records (Deviations, CAPA, Change Control) with Cell Therapy Hub and QA.

  • Travel up to 50%.

You Have:

  • Bachelor’s degree (Nursing, Physician Assistant) with thorough knowledge/hands-on experience in Cell Therapy.

  • 8+ years' experience in cell therapy with progressive leadership.

  • Expertise in service lines (infrastructure, resourcing, costs, quality metrics).

  • Proven delivery to timelines, cost, and quality; collaboration with internal/external providers.

  • Excellent knowledge of cell therapy standards/regulations.

  • Experience selecting/overseeing external providers and developing contracts.

Nice to Have:

  • Advanced scientific degree; broad understanding across patient operations, manufacturing interfaces, quality, regulatory, market access; project management experience.

  • Program/Quality qualifications (e.g., PMP, CPHQ).

  • Experience across academic/Sponsor settings and countries.

  • Early-phase delivery across product lifecycle and multiple therapeutic areas.

  • Salesforce or similar CRM experience.

#celltherapy

The annual base pay for this position ranges from $150,000 to $225,000. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Date Posted

18-May-2026

Closing Date

26-May-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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