AD/ Principal Scientist CMC AAV Gene Therapy

Ocugen; Malvern (Chester County); On-site; USD 180,000 - 240,000; Full time

Job summary

Ocugen in Malvern, PA seeks an experienced CMC leader to drive BLA-stage readiness for AAV gene therapy programs. You will bridge development, GMP manufacturing, regulatory affairs, and program leadership to ensure a smooth transition from clinical development to licensure.

You will author Module 3 content, oversee DS/DP, analytics, stability, and validation, and support regulatory interactions through approval. This high-visibility role requires deep AAV manufacturing and lifecycle expertise.

Qualifications

• Ph.D. (preferred) or Master’s in Biochemical Engineering, Biotechnology, Pharmaceutical Sciences, or related field.
• 10+ years in biologics or AAV gene therapy CMC development.
• Direct experience leading or significantly contributing to BLA-stage submissions.
• Deep knowledge of AAV manufacturing platforms and potency assay development.
• PPQ and process validation for biologics; stability and shelf-life justification.
• Regulatory expectations for gene therapy products; experience supporting FDA meetings and pre-approval inspections.

Responsibilities

• Lead development and authoring of CMC sections (Module 3) for BLA submission.
• Integrate DS, DP, analytical, validation, stability, and control strategies into regulatory narratives.
• Develop control strategy lifecycle and comparability frameworks.
• Coordinate data readiness across functions to meet BLA timelines.
• Lead responses to FDA information requests and potential Advisory Committee support.
• Provide strategic oversight of process characterization, viral clearance, PPQ protocol, CPV planning.
• Drive pre-approval inspection readiness and ensure manufacturing consistency across batches.

Skills

CMC leadership

BLA submissions

GMP manufacturing

Regulatory affairs

Cross-functional leadership

AAV manufacturing

PPQ strategy

Statistical analysis

Education

Ph.D. (preferred)

Job description

Position Summary

We are seeking an experienced CMC leader to drive BLA-stage readiness for AAV gene therapy programs. This role serves as the strategic technical interface between laboratory development, GMP manufacturing, regulatory affairs, and program leadership to ensure seamless transition from clinical development to licensure.

Position Summary

We are seeking an experienced CMC leader to drive BLA-stage readiness for AAV gene therapy programs. This role serves as the strategic technical interface between laboratory development, GMP manufacturing, regulatory affairs, and program leadership to ensure seamless transition from clinical development to licensure. The individual will lead CMC integration across drug substance (AAV vector production), drug product (formulation and fill-finish), analytical characterization, process validation (PPQ), comparability strategy, and stability programs. A core responsibility of this role is authoring and coordinating high-quality Module 3 content for BLA submission and supporting regulatory interactions through approval. This is a high-visibility role requiring deep expertise in AAV manufacturing science, regulatory expectations, and lifecycle management.

Responsibilities

• Lead development and authoring of CMC sections (Module 3) for BLA submission.
• Integrate DS, DP, analytical, validation, stability, and control strategy into cohesive regulatory narratives.
• Develop and justify:
  • Control strategy and specification lifecycle
  • Comparability frameworks (process changes, site transfers, scale-up)
  • Process validation and PPQ strategy
• Coordinate data readiness across functions to meet BLA timelines.
• Lead preparation of responses to FDA information requests, late-cycle review questions, and potential Advisory Committee support.

Process Validation & Commercial Readiness

• Oversee phase-appropriate transition to commercial-scale AAV manufacturing.
• Provide strategic oversight of:
  • Process characterization studies
  • Viral clearance (if applicable)
  • PPQ protocol development and execution
  • Continued Process Verification (CPV) planning
• Ensure control strategy is statistically justified and aligned with ICH Q8/Q9/Q10 principles.
• Drive readiness for pre-approval inspection (PAI).
• Drug Substance (AAV) Oversight
• Provide technical leadership in:
  • Upstream (cell expansion, transfection/infection systems)
  • Downstream purification (chromatography, TFF, clarification)
  • Empty/full capsid ratio control
  • Vector genome integrity and potency assays
• Ensure manufacturing consistency across clinical and commercial batches.
• Lead technical assessment of critical process parameters (CPPs) and critical quality attributes (CQAs).
• Drug Product & Stability Strategy
  • Oversee formulation optimization, aseptic fill-finish readiness, and container closure integrity.
  • Ensure stability program supports shelf-life justification at BLA.
  • Drive extractables/leachables, shipping validation, and in-use stability readiness.
• Comparability & Lifecycle Management
  • Lead comparability strategy across:
    • Phase 1 to Phase 3 evolution
    • Manufacturing scale changes
    • Site transfers or CDMO transitions
  • Develop risk-based justification when formal comparability protocols were not historically implemented.
  • Ensure analytical depth supports regulatory defensibility.
• Cross-Functional & CDMO Interface
  • Serve as primary CMC integration lead across:
    • Process Development
    • Analytical Development
    • MSAT
    • Quality
    • Regulatory Affairs
  • Act as senior technical liaison with CDMOs, ensuring alignment on validation, documentation, and regulatory positioning.
  • Maintain disciplined communication pathways for regulatory-sensitive decisions.

Qualifications

• Ph.D. (preferred) or Master’s in Biochemical Engineering, Biotechnology, Pharmaceutical Sciences, or related field.
• 10+ years in biologics or AAV gene therapy CMC development.
• Direct experience leading or significantly contributing to BLA-stage submissions.
• Deep knowledge of:
  • AAV manufacturing platforms
  • Potency assay development and validation
  • PPQ and process validation for biologics
  • Stability and shelf-life justification
  • Regulatory expectations for gene therapy products
• Experience supporting FDA meetings and pre-approval inspections.
• Strong program leadership and cross-functional execution skills.

Preferred Experience

• Experience with at least one AAV program through BLA submission or approval.
• Expertise in empty/full capsid analytics and advanced characterization.
• Experience with multi-site tech transfer or commercial launch preparation.
• Familiarity with global filings (EMA, PMDA).

Working Conditions

This position operates in an office setting, in person. Job may additionally require incumbent to be available outside of these hours to handle priority business needs.

Ocugen is an equal opportunity employer. In order to provide equal employment and advancement opportunities to all individuals, we make all of our employment decisions based upon merit, qualifications, abilities, and an individual’s conduct and performance. We will not make any of our decisions, and will not discriminate against any employee or applicant, on the basis of race, color, religion, creed, national origin or ancestry, ethnicity, sex (including pregnancy), gender (including sexual orientation, gender identity and status as a transgender or transsexual individual), age, physical or mental disability, citizenship, past, current or prospective service in the uniformed services, genetic information, or any other characteristic protected from discrimination under the law. Ocugen complies with applicable federal, state and local laws governing nondiscrimination in employment.