What are the responsibilities and job description for the Director, Upstream Cell Culture Process Development and Manufacturing (Biologics) position at Tbwa Chiat/Day Inc?
Director, Upstream Cell Culture Process Development and Manufacturing (Biologics)
Waltham, Massachusetts, United States
About Us :
Oruka Therapeutics (Nasdaq : ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka’s mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. We have raised nearly $500M since inception in February 2024 from top-tier investors and our first program is expected to be in the clinic in the first quarter of 2025. For more information, visit www.orukatx.com.
As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture.
Position Overview :
We are seeking an experienced and motivated candidate to lead early-stage IND enabling cell line and cell culture process development and manufacturing activities. In this role, the ideal candidate will be responsible for overseeing cell line and process development, tech transfer, scale-up and clinical DS manufacturing of monoclonal antibodies at the CDMOs. The successful candidate will establish CMC strategy for early-stage process development, perform gap assessment, and provide timely solutions while continuing to plan late-stage development. In this role, you will oversee activities at the CDMO partners to track and ensure timely completion of GMP drug substance manufacturing. This role involves drafting high quality reports, finalization of source documents and active participation in writing regulatory submissions. You will be an integral part of the team with an opportunity to work in a fast-paced environment.
Key Responsibilities :
- Manage cell line development, clone selection / stability, cell banking, cell culture development, and manufacturing operations at the CDMOs for multiple programs.
- Work with the CDMO to optimize cell culture unit operations with an emphasis on robustness, scalability, quality, cost, validation with line of sight to commercial manufacturing.
- Build strong relationships and partners with other leaders across Development, Quality, Regulatory, and external CDMOs.
- Lead cell culture manufacturing with the CDMO ensuring seamless execution and timely completion.
- Manage the diligence process to select commercial DS CDMOs.
- Serve as subject matter expert and enable successful tech transfer to commercial CDMOs.
- Serve as person-in-plant (PIP) during drug substance manufacturing campaigns.
- Apply QbD principles to develop process parameters and product quality relationships to aid process optimization in support of late-stage development.
- Partner with stakeholders to support timely approval and execution of reports, batch records, in-process sampling plans, review SOPs, change controls, deviations, OOS / OOT investigations, and CAPAs.
- Support regulatory filings by authoring, reviewing, and approving technical reports, CMC sections of clinical and registration submissions (INDs / BLAs), and responses to questions.
- Perform CMC risk assessment activities in a phase appropriate manner ensuring proper measures are in place in support of production and filing requirements.
- 20-25% travel in support of manufacturing activities at the CDMOs.
Minimum Qualifications :
Compensation :
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We're looking forward to hearing how you can contribute to our team and mission. Join us in shaping the future of our company and making a real impact every day.
What We Offer :
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