Group Lead, Manufacturing
Listed on 2026-08-09
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Manufacturing / Production
Quality Engineering, Pharmaceutical Manufacturing, Manufacturing & Industrial Operations, Regulatory Compliance Specialist
About Site
Our FDA-licensed, state-of-the‑art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities is located 5 miles from the Baltimore Washington International (BWI) airport and 13 miles from our Baltimore location. The campus is close to Washington, DC’s I-270 Technology Corridor, top universities, and government agencies.
About SiteOur FDA-licensed, state-of-the‑art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities is located 5 miles from the Baltimore Washington International (BWI) airport and 13 miles from our Baltimore location. The campus is close to Washington, DC’s I-270 Technology Corridor, top universities, and government agencies. The Harmans/BWI-1 EMA and FDA approved facility, at approximately 200,000 sq.
ft., houses 10 CGMP manufacturing suites, fill/finish, central services, testing labs, and a warehouse. The Harmans/BWI-2 facility, at approximately 145,000 sq. ft., is under development and will house 8 CGMP manufacturing suites and cold storage warehousing. Both facilities support Phase 3 through commercial manufacturing of advanced therapeutic products including AAV and other viral vector-based therapies and vaccines.
We have an opportunity for a Group Lead, Manufacturing to join our team. In this role, you will support the execution of clinical and commercial manufacturing in compliance with GMP standards. You will help drive process optimization, efficiency, and continuous improvement to maximize capacity. This position combines hands‑on production with leadership responsibilities to ensure safe, compliant, and efficient operations. You will play a key role in guiding the team and supporting the transfer of new projects into GMP production.
ShiftNight shift, 7pm-7m on a 2-2-3 rotating schedule
LocationHarmans, MD - BWI
Work Hours100% Onsite
The Role- Provide day‑to‑day leadership and work direction for Manufacturing Associates and Technicians, including indirect supervisory responsibilities.
- Lead Tier 1 operational meetings and drive performance across safety, quality, delivery, cost, and employee engagement metrics.
- Promote operational excellence and continuous improvement initiatives, acting as a change agent to enhance manufacturing efficiency and effectiveness.
- Support rapid issue resolution by troubleshooting process and equipment challenges and partnering with Facilities, Validation, and Engineering teams.
- Ensure personnel are properly trained and compliant with cGMP requirements, manufacturing procedures, documentation practices, and safety standards.
- Complete, review, and revise manufacturing documentation, including Batch
- Production Records (BPRs), Standard Operating Procedures (SOPs), and related GMP records.
- Collaborate with Process Development, Manufacturing Sciences & Technology (MS&T), and Production Management to support technology transfers, new product introductions, and manufacturing projects.
- Lead or support deviation investigations, CAPAs, validation activities, facility expansions, and continuous process improvement initiatives.
- Serve as a key manufacturing representative for clients, cross‑functional teams, and external stakeholders, supporting manufacturing campaigns, project execution, and production readiness.
- Perform other duties as assigned.
- Bachelor’s or Master’s degree in a technical discipline (e.g., biology, biotechnology, engineering) or related life science field with a minimum of 4 years of related experience, OR Associate’s degree with a minimum of 6 years of related experience, OR High School Diploma with a minimum of 7 years of related experience
- Outstanding knowledge and ability to apply scientific principles to solve operational and routine production tasks
- Demonstrated focus on safe behaviors and ability to recognize unsafe conditions
- Thorough understanding of quality systems in a regulated environment and commitment to right first time (RFT) execution
- Excellent documentation skills including comprehension, review, and establishing Batch Production…
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