Director, Manufacturing Job at Neurogene Inc. in Houston

Director, Manufacturing – Neurogene Inc.

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Overview

The mission of Neurogene is to treat devastating neurological diseases to improve the lives of patients and families impacted by these rare diseases. Neurogene is developing novel approaches and treatments to address the limitations of conventional gene therapy in central nervous system disorders. This includes selecting a delivery approach to maximize distribution to target tissues and designing products to maximize potency and purity for an optimized efficacy and safety profile. The Company’s novel and proprietary EXACT transgene regulation platform technology allows for the delivery of therapeutic levels while limiting transgene toxicity associated with conventional gene therapy. Neurogene has constructed a state‑of‑the‑art gene therapy manufacturing facility in Houston, Texas. CGMP production of NGN‑401 was conducted in this facility and will support pivotal clinical development activities. This transformative work is driven by our highly collaborative people who come together each day to bring us closer to achieving our mission. As an employee of Neurogene, you will be part of building a culture that honors patient and caregiver mindsets and nurtures innovation, creative problem solving and a strong sense of purpose.

Responsibilities

• Provide strategic and operational leadership of GMP Manufacturing operations with responsibility for ensuring uninterrupted production of clinical and commercial gene therapy products.
• Lead, develop, and mentor a cross‑functional team of manufacturing staff and managers to deliver on production goals, operational excellence, and compliance.
• Serve as a key contributor to the manufacturing leadership team, ensuring alignment with overall company objectives and timelines.
• Act as primary manufacturing liaison with cross‑functional teams including Quality, Regulatory, Analytical Development, Supply Chain, and Process Development to support tech transfers, deviations, CAPAs, and continuous improvement initiatives.
• Drive implementation of lean manufacturing principles and quality by design (QbD) strategies to enhance process robustness and reduce variability.
• Oversee execution and review of batch records, ensuring compliance with cGMPs and internal quality standards.
• Support inspection readiness activities and directly interface with regulatory agencies and partners as required.
• Contribute to manufacturing strategy development, budgeting, headcount planning, capital projects, and new technology implementation.
• Oversee execution of the Process Performance Qualification (PPQ) strategy and associated manufacturing campaign, ensuring alignment with process validation plans, quality system requirements, and regulatory expectations.
• Represent Manufacturing in CMC regulatory submissions and participate in preparation of BLA/MAA filings.
• Ensure documentation is completed to meet quality systems requirements.
• Work with Quality Assurance to achieve and maintain GMP readiness and compliance in manufacturing.
• Participate in facility safety programs.
• Hire, train, and supervise direct reports, and encourage continuing education and development.

Essential Details

Work Schedule: Day shift (some off‑shift hours: early mornings, late evenings/nights, and weekends if necessary)

Travel: <10%

Safety

• Is knowledgeable and complies with all pertinent safety policies, rules and regulations.
• Ensure that all team members comply with safety rules and regulations.

Quality Responsibility

Maintenance of quality systems and cGMP compliance for the business by ensuring that all team members comply with processes, procedures and instructions for all activities in which the team participates.

Scope

Works on issues of diverse scope where analysis of situation or data requires a review and evaluation of identifiable factors. Exercises judgment within defined procedures and policies in selecting methods and techniques in obtaining solutions and in determining appropriate action.

Leadership Responsibility

Provides appropriate coaching and performance feedback to all direct reports and ensures that all team members are being developed.

Minimum Requirements

Bachelor’s degree in Biology, Biotechnology, Engineering, or a related discipline is required. Advanced degree (MS, MBA, or equivalent) preferred.

Experience

• 10+ years of progressive experience in GMP biologics or gene therapy manufacturing, including 5+ years in a people management or leadership role.
• Proven experience leading cross‑functional projects and tech transfers in a regulated environment.
• Direct experience with AAV vector production using adherent or suspension cell culture systems (HEK293, Sf9/Baculovirus, or other platforms).
• Prior involvement in late‑phase or commercial stage manufacturing and regulatory submissions (e.g., PPQ, BLA, MAA) is a plus.

Knowledge

• Deep understanding of cGMP, FDA, and global regulatory requirements for biologics or ATMPs.
• Strong technical acumen in upstream and/or downstream processes and equipment.
• Excellent leadership and interpersonal skills with demonstrated ability to build and lead high‑performing teams.
• Effective communicator with ability to influence across departments and levels.
• Strong analytical, organizational, and decision‑making capabilities.
• Comfortable in a dynamic, fast‑paced startup or biotech environment.

Skills

• Understanding of the principles of biologics manufacturing.
• Experience with all aspects of cell culture methods and techniques including large‑scale culture.
• Experience with large‑scale purification operations.
• Technical acumen with single‑use technologies in biologics manufacturing.
• Understanding of the operating principles for aseptic manufacturing.
• Strong communication skills, both written and oral.
• Able to develop new procedures when required.
• Demonstrate skills in problem‑solving and provide solutions.
• Interact effectively with staff members from multiple levels and departments.
• Strong organizational skills and ability to manage and prioritize multiple projects or assignments at one time, including following assignments through to completion and meeting deadlines.
• Ability to lift 50lbs, assisted.
• Demonstrated strength as a supervisor including mentoring and coaching of staff, establishing priorities, and delivering on projects within budget and on time.

Working Conditions

A majority of the work is done in a private office, warehouse or manufacturing environment. The manufacturing environment is a clean room where appropriate gowning is required to be worn. Work may involve high energy hazards, such as steam, high pressure gases, flammable materials, high temperature liquids and high voltage, cryogenic operations, loud machinery and chemical hazards such as strong acids and bases.

Seniority Level

Director

Employment Type

Full‑time

Job Function

Management and Manufacturing

Industry

Biotechnology

Location

Houston, TX