Scientist, Engineering Full-time

Upstream Process Development Scientist

As part of Our Company’s Manufacturing Division, the Upstream department provides the technical process leadership and laboratory capabilities in support of late-stage pipeline and post-market commercial manufacturing processes for the upstream portion of vaccines drug substance processes. VDSC supports various commercialization activities, early and late stage process development, second generation process development including process characterization, technology transfer to internal and external manufacturing sites, manufacturing investigations, process validation, and authoring of regulatory submissions.

We are seeking individual contributors with strong scientific and technical skills to support development and commercialization activities supporting multiple vaccine programs in late stage development.

In this role, the successful candidate will be responsible for:

• Function as a key member of the team executing large molecule upstream process development activities including lab-scale process development and process scale-up/scale-down
• Executing lab scale experiments and authoring associated technical reports and documents
• Leading assignment execution against accelerated, critical-path timelines in a right-first-time manner
• Contributing to and/or authoring technical documents to support Process Performance Qualification (PPQ) and licensure
• Collaborating with commercial manufacturing teams to support facility start-up activities and provide on-the-floor support for drug substance manufacturing, both within our Company’s network and at contract manufacturing organizations (CMOs)
• As an individual contributor, will have clearly identifiable elements or functions within a larger project team. May oversee and coordinate work performed by contractors.

Education Minimum Requirement:

• B.S. in Chemical Engineering, Biochemical Engineering, Bio-engineering, Pharmaceuticals, Biochemistry, Microbiology, or related field with 2+ years of relevant experience; or
• Master’s degree with 1+ years of relevant experience; or Ph.D. with relevant experience.

Required Experience and Skills:

• Large molecule process development, or relevant experience including scaling (up and down) and tech transfer/facility fit of large molecule drug substance processes
• Good understanding of microbial physiology and metabolism and ability to correlate to in-lab or shop floor fermentation events
• Experience with small, lab, or pilot-scale large molecule fermentation and cell culture processes such as use of fermentors, bioreactors, and/or static cell culture
• Expertise in lab scale experimental execution and experience with statistical data analysis (JMP, PI Vision, Spotfire, SIMCA, etc.) including presentation of results/conclusions.
• Experience with authoring technical documentation.
• Outstanding communication and people skills.
• Proven ability to work independently and as a part of a team, executing against key commitments.
• Ability to foster a collaborative work environment
• This role may require working outside of core business hours to support lab studies and/or on-site activities related to tech transfer and manufacturing.

Preferred Experience and Skills:

• Knowledgeable in Drug Substance, end-to-end process development, including microbial, live virus vaccine, gene therapy, or oncolytic virus processes.
• Upstream process development and manufacturing sciences knowledge.
• Experience in current Good Manufacturing Practices (cGMP), Quality by Design (QbD) and Lean Six Sigma principles.