Senior Process Engineer, Manufacturing, Science, and Technology (MSAT) Cell Therapy

AstraZeneca plc; Rockville (MD); On-site; USD 103,000 - 155,000; Full time

Benefits offered by this job

Health, dental, and vision coverage

Retirement plan

Paid time off

Job summary

AstraZeneca plc Rockville, MD is seeking a Senior Process Engineer for MS&T in cell therapy. You will lead on-the-floor support, drive CAPAs, and support tech transfer, validation, and regulatory readiness.

Strong GMP experience in cell therapy is required, with a focus on data-driven improvements across campaigns. The role emphasizes cross-functional collaboration, documentation, and continuous improvement within a fast-paced manufacturing environment.

Qualifications

• Hands-on experience in cell therapy unit operations in GMP environments.
• Experience with process development, tech transfer, and validation activities.
• Ability to lead complex deviation investigations and CAPA work.

Responsibilities

• Provide on-the-floor technical support for cell therapy campaigns.
• Lead deviation investigations and CAPA implementation with data.
• Support technology transfer, PPQ, and process validation activities.
• Draft and revise batch records, SOPs, and technical reports.
• Collaborate with QA, Supply Chain, and global teams on lifecycle management.
• Assist in regulatory documents and inspections readiness.

Skills

Cell therapy operations

GMP experience

Data analysis

Statistical analysis

Technical writing

Cross-functional collaboration

Education

PhD in Chemical/Biochemical Engineering or related field

MS in Chemical/Biochemical Eng or related field

BS in Chemical/Biomedical/ Biotech Eng or related field

Job description

Senior Process Engineer, Manufacturing Sciences & Technology, Cell Therapy:

Location: AstraZeneca, Rockville, MD

Travel: Up to 15%domesticand international travelrequired

Position Summary

We are seeking an experienced Senior Process Engineer to join our Manufacturing Sciences & Technology (MS&T) function as a member of the site-based MS&T team at AstraZeneca’s Rockville, MD cell therapy manufacturing facility.

This position focuses on ensuring robust, compliant, and cost-effective manufacturing of clinical and commercial cell therapy products.

Responsibilities include leading on-the-floor / hands-on technical support, developing technical instructions, procedures, and operator training content, performing data analysis and process performance trending, leading complex deviation investigations, driving implementation of CAPAs and continuous improvement through change controls, and giving to validation and regulatory work. These responsibilities will be exercised through the scope of supporting technology transfers, clinical manufacturing, site readiness, process validation/PPQ, commercial manufacture readiness, andproductlifecycle management activities.

The ideal candidate brings hands-on experience with cell therapy unit operations throughpreviousexperience in process development and/or manufacturing, as well asexpertisein technology transfer. Experience with process validation and commercialization activities is desired. This position will report to Director, MS&T, Cell TherapyDevelopmentand Operations.

Key Responsibilities

Site manufacturing support

• Process Execution Support: Provide day-to-day technical support for cell therapy manufacturing, including on-the-floor support for critical campaigns (including occasional off-shift support whererequired)
• Operations Support: Represent Site MS&T function at site operational tier meetings, providing collaborative inputs that drive site activities
• Data trending and analysis:Maintainmanufacturing data tracking system and control charts, perform trend analyses,identifysignals, and drivetimelysignal-to-action with clear documentation and multi-functional alignment.
• Process performance monitoring: Conduct batch record review, deviation assessment, and data trending to ensure robustness of cell therapy manufacturing processes.
• Deviation/CAPA Support: Lead or co-lead technical investigations for deviations and process excursions, perform root cause analysis,developand implement CAPAs withappropriate data.
• Continuous improvements:Identify, justify, and implement continuous improvements by shepherding changes through multi-functional change controls withappropriate riskassessments and comparability.
• Raw materials: Support qualification of critical materials (e.g., cytokines, viral vector, single-use assemblies) and assess impact of raw material changes, and supply to second-source strategies
• Automation: Partner with automation/digital manufacturing teams to implement electronic batch record improvements
• Documentation & GMP Compliance: Author and revise batch records, SOPs, and technical reports; protocols, summary reports, ensure alignment to cGMP/ATMP requirements and data integrity principles (ALCOA+).
• Training & Knowledge Transfer: Deliver operator training on critical process steps or process changes; chip in to lessons-learned, playbooks, and guidelines across sites.
• Regulatory Contributions: Draft and review CMC sections (Module 3) response to agency question, support healthauthorityand internal audits/inspections.

Technology Transfer & Process Validation

• Draft and review risk assessments and comparability study design
• Chip in to technology transfer packages (process descriptions, URS inputs, BOMs, risk assessments), implement process changes, coordinate execution of engineering runs and comparability/bridging studies, author technical reports
• Translate process characterization outputs from development into manufacturing controls, and draft sections of PPQ protocols/reports
• Provide on‑the‑floor technical support during scale‑up, engineering runs, PPQ batches, and commercial manufacturing campaigns (including off‑shift support whenrequired).

Multi-functional Collaboration

• Position serves as primary interface between site Manufacturing, site Quality, site Supply Chain, and global functions of Process Development and CMC regulatory
• Support lifecycle management for cell therapy processes, including continuous improvement initiatives and post-approval changes

Required Qualifications

Minimum Education and experience:

B.S. with 8+ years ofhandsonindustry experience. M.S. with 4 years ofhandsonindustry experience, PhD in Chemical Engineering, Biochemical Engineering, Biotechnology, or related field with 1+ years of industry experience

Technical Skills

• Strong technical and hands-onexpertisein key cell therapy unit operations and common cell therapy processing equipment
• Demonstratedexperience working in GMP environments, including batch record execution or review, deviations, and investigations.
• Proficiencywith statisticalanalysis(including univariate, multi-variate analysis, control charts)
• Provenability inaccurateand thorough technical writing, paired with clear and concise verbal communication
• Strong data analysis, and problem‑solving skills.

Soft skills

• Excellent multi-functional communication and collaboration.
• Ability to translate complex data into clear decisions and regulatory-ready narratives.
• Excellent problem solving, multi-functional leadership, and communication under time-sensitive conditions.

Preferred Qualifications

• Experience with late‑stage clinical manufacturing support of cell therapy products
• Experience with process validation and commercial readiness of cell therapy products

Work Environment

• On-site in Rockville, MD
• Ability to travel ~15% to other manufacturing facilities
• On-call rotation during engineering/PPQ/critical campaigns

The annual base pay (or hourly rate of compensation) for this position ranges from $103,286.40to $154,929.60.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 coveragein accordance withthe terms of the applicable plans.

Date Posted

22-Sep-2026

Closing Date

15-Oct-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.