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Head of Manufacturing
CARsgen Therapeutics CorporaDurham, North Carolina, US- Promoted
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CARsgen Therapeutics CorporaDurham, North Carolina, US- Full-time
All candidates should make sure to read the following job description and information carefully before applying.
Purpose and Scope of Position :
CARsgen is looking for a senior Manager of CAR-T cell therapy manufacturing. The role will report to the head of Technical Operations and is responsible for managing the daily clinical manufacturing activities of CT053, CT041 and other CAR-T cell products at the US Durham, NC facility. The position will also supervise the manufacturing staff, ensure GMP trainings and compliance, plan the productions, and champion various initiatives aimed at improve quality and efficiency. This position will also play a key role in tech transfers. This person is a key member of the site leadership and will serve as an operating steward the US site.
Duties and Responsibilities :
- Lead manufacturing team in planning and executing CAR-T cell therapy productions to meet clinical needs.
- Collaborate closely with MST and other functions to execute tech transfers to RTP site
- Manage cleaning staff / contractors to ensure manufacturing areas are cleaned per established SOPs
- Build effective cross-functional collaborations with Quality, Supply Chain, MS&T, EHS and Facilities.
- Ensure a culture that embraces safety in the work environment and safety of the patients through compliance with company procedures, policies, and cGMP requirements.
- Set goals, tracking and KPIs, and driving continuous improvement through operational excellence, technical advancement and lean manufacturing initiatives.
- Establish a manufacturing management systems that are technically sound, promote efficient operations, and comply with cGMP requirements.
- Ensure schedules of the people, facility, equipment, materials, and documents are well organized to support the expected capacity for CAR-T manufacture. Identify and mitigate risks in manufacturing operations that could negatively impact delivery of safe and effective therapies to patients.
- Lead major investigations related to manufacturing. Ensure on time closure of deviations, CAPAs, and change controls.
- To shape and develop a fit for purpose department organization and an inclusive high performing business team, continuously improve team efficiency through effective management methods, such as fair and objective performance evaluation on the team members and effective internal communication.
- Develop and implement the internal training programs for the manufacturing team to improve the productivity and ensure compliance
- Establish management policie, shift structure, and career ladders for Associates and supervisors
- Draft, review and approve various GMP documents, including standard operating procedures, batch records, material specifications, and validation protocols / reports.
- Up to 5% travel may be required.
Qualifications and Experience :
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