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Senior Engineering Manager, Frontline Support

2 months ago

Vacaville, California, United States Genentech Full time

This role is an integral part of our Genentech Vacaville site, one of the largest cell culture manufacturing facilities in the world. As a Senior Engineering Manager, you will be responsible for leading and managing a team of equipment/automation engineers and manufacturing specialists to support our large-scale, fast-paced, and dynamic manufacturing operations, also known as Make, Assess, Release (MAR). This team works to ensure reliable system performance, investigates major equipment events, and contributes to the successful transfer of new processes into the facility.

The Opportunity:

As a Senior Engineering Manager, you will leverage your leadership and exceptional problem-solving capabilities to coach and develop people, drive continuous improvement, and set priorities. You will collaborate closely with key stakeholders across various functions to support the delivery of high-quality drug substances. Additionally, you will:

  • Be accountable for process equipment performance, resolution of production issues, and partner with plant management to meet manufacturing goals and objectives
  • Assign roles and responsibilities to support daily plant operations, facilitate investigation strategies, and present in audits and governance meetings
  • Support the advanced troubleshooting of complex manufacturing systems, facilitate options analyses, train and develop staff, lead the development of improvement projects, and contribute to the project scope and requirements for larger projects

Who You Are:

  • You possess a Bachelor's degree in Engineering or Life Science AND 12 years of demonstrated expertise in engineering operations
  • You possess industry experience in biotech/pharmaceutical or other regulated industry
  • You have at least 5 years of people leadership experience
  • You have at least 5 years of experience with Upstream or Downstream Commercial Cell Culture processing
  • You are proficient in cGMP or equivalent regulations as they apply to biopharmaceutical manufacturing facilities
  • You have experience in managing quality records, including developing investigation strategies, determining potential product impact, and implementing short and long-term solutions
  • You possess an in-depth knowledge of equipment including sanitary design requirements and ASME BPE requirements
  • You have the demonstrated ability to independently evaluate situations and propose effective and sound solutions

Relocation is approved for this position.

The expected salary range for this position is based on the primary location of California is $132, ,830. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. 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.

Benefits

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Genentech is an equal opportunity employer, and we embrace the increasingly diverse world around us. Genentech prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status and veteran status.