Technical Development Principal Engineer

Genentech • Daly City, CA

1d • Onsite

About The Position

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche! As part of Pharma Technical Development (PTD) our organization is committed to deliver the Pharma ambitions by bringing game-changing therapies from clinical phase I into the market to serve every patient, every day. Our core business is to develop safe, innovative and effective drugs using cutting edge technologies for manufacturing process (Drug Substance and Drug Product), clinical supply, formulation, device, packaging, and analytical development. As an integrated partner within the drug development ecosystem, Global Biologics Pharmaceutical Development is dedicated to effectively developing innovative and patient-centered parenteral drug products including Formulation and Process Development and Drug Delivery Systems.

Requirements

• B.S., M.S., or Ph.D. in chemical engineering, pharmaceutical sciences, chemistry, bioengineering or a related engineering discipline.
• Relevant biopharmaceutical industry experience preferred, 2+ years with Ph.D, 5-6+ years with M.S., 8+ years with B.S.
• Expertise in process development for large molecule parenteral Drug Product pharmaceuticals with demonstrated experience implementing processes in a clinical or commercial manufacturing facility.
• Expert-level ability to translate expertise in chemical engineering, chemistry and biology into a first principles understanding of DP processes and the underlying chemistry. (ex. Able to develop and experimentally verify a model)
• Excellent analytical and problem solving abilities, hands-on experience with protein processing, lab techniques, and instrumentation.
• Excellent written and verbal communication skills and the ability to interact and influence in a multi- disciplinary group setting.
• Knowledge of GMP documentation principles.
• Knowledge of relevant standards, guidance for industry, and regulatory statutes.
• Ability to manage several multi-faceted, cross-functional projects.

Responsibilities

• Develop and support Drug Product pharmaceutical processes and technology including freeze/ thaw, mixing, filtration, filling, lyophilization, sterilization, etc.
• Design appropriate small scale models to understand mechanisms and derisk at-scale processes.
• Interact and collaborate with other functions including PTD, Quality, Regulatory, Commercial, and Manufacturing organizations in cross-functional projects.
• Author, review, and approve internal technical, development, validation, and manufacturing documents, including protocols, regulatory filings, SOPs etc.
• Lead development and qualification studies, technology transfers, and new technology investigations.
• Interact with project teams and leadership to communicate results and drive projects.

Benefits

• Relocation benefits are available for this job posting.
• A discretionary annual bonus may be available based on individual and Company performance.
• This position also qualifies for the benefits detailed at the link provided below.

What This Job Offers

• Job Type: Full-time
• Career Level: Principal
• Education Level: Ph.D. or professional degree