Senior Scientist, Engineering- Cell Banking

Job Description

Our Scientists and Engineers support internal development and internal/external manufacturing operations to remain operational, continuously improve, and innovate. With our extensive range of facilities and environments, our Scientists have opportunities across many diverse areas including Biological, Chemical, Automation, Safety, Technical Services, Process Development, Analytical, Regulatory, and Quality.

As part of Our Company’s Manufacturing Division, within the Biologics Drug Substance Commercialization (BDSC) organization, the upstream process science and technology department provides the technical process leadership and laboratory capabilities in support of late-stage pipeline and post-market commercial manufacturing processes for vaccines and biologics. The group supports various cell bank and upstream drug substance process commercialization activities and second generation process development including cell banks, process characterization, technology transfer to internal and external manufacturing sites, manufacturing investigations, process validation, and authoring of regulatory submissions.

Under the general scientific and administrative direction of Director, Engineering, and working in conjunction with internal and external partners, this person will support mid-late stage and commercial cell bank-related projects for large molecule programs. The person will be responsible for commercialization activities on late-stage pipeline and/ or post-market commercial manufacturing working cell banks for biologics and/or vaccines. Activities include cell bank process assessments and transfers, manufacturing investigations and trend evaluations, process characterization, new WCB qualification, and regulatory submission authoring, with a focus on standardization across programs.

Technical scope:
Direct projects focusing on cell bank process risk assessments, documentation, process characterization, technology transfer and qualification of new cell banks with line-of-sight for licensure and commercialization. Responsible for planning and executing work to support commercialization of working cell banks, identification and implementation of process changes for replenishment lots, control strategies, manufacturing operations, investigation evaluations, and regulatory filings.

Lead assignment execution against accelerated timelines, in a right-first-time manner, with a “safety first, compliance always” mindset. Minimum Required

Education and Experience:

Bachelor’s Degree in Biochemistry, Bioengineering, Biochemical Engineering, Biological Engineering, or Chemical Engineering with five (5) years of cell culture experience in pharmaceutical industry; OR Master’s degree in Biochemistry, Bioengineering, Biochemical Engineering, Biological Engineering, or Chemical Engineering with three (3) years of cell culture experience in pharmaceutical industry; OR Ph.D. in Biochemistry, Bioengineering, Biochemical Engineering, Biological Engineering, or Chemical Engineering. Required Expertise and

Skills:

Fundamental understanding of cell line development, cell culture growth metabolism, cell death, and media adaptation. Hands-on experience and expertise in mammalian and/or microbial, adherent and/or suspension cell culture, including cell enumeration and expansion, virus infection, cryopreservation, cell bank preparation, and laboratory scale process operations in cell culture stacks, shake flasks, and/or 2-3L bioreactor systems. Experience authoring technical documentation to support regulatory submissions.

Outstanding communication and people skills. Ability to foster a collaborative work environment, focused on common goals and working across boundaries. Acute problem-solving skills, project management, and keen ability to navigate work in an ambiguous environment.

Preferred

Skills:

Large molecule cell line/process development, including laboratory and/or GMP manufacturing of upstream processes. Hands-on expertise with mammalian cell culture bench scale and ability to oversee teams through these requirements as lab lead. Experience with on-the-floor Good Manufacturing Practice (GMP) manufacturing support, manufacturing batch record reviews and/or operations. Expertise with Quality by Design (QbD) and Lean Six Sigma principles. Working understanding of US/EU regulatory requirements and analytical methods required to ensure viral safety and characterization of cell banks, and working knowledge of cGMP principles and regulations.

Expertise supporting/writing regulatory filings (IND, MAA, BLA) and inspections with multiple agencies (FDA, EMA, JNDA, TGA).