Genentech

Associate Automation Engineer

Genentech$61K — $114K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s or Master’s degree in Engineering or related scientific discipline.
  • 0-2 years of experience in automation or related technology field.
  • Familiarity with programming tools like Python and data visualization concepts.
  • Demonstrated problem-solving skills in ambiguous situations.
  • Strong interpersonal skills for teamwork and communication.

Responsibilities

  • Own and execute small to medium scope automation engineering projects.
  • Collaborate with senior engineers to suggest data-driven improvements.
  • Support generation and review of qualification protocols.
  • Participate in drafting and updating GMP Lifecycle Documents.
  • Manage change records and track business process updates independently.
  • Collaborate in troubleshooting and support of automation systems.
  • Maintain mandatory training qualifications and seek technical knowledge.

Benefits

  • Opportunities for learning and development in automation and data technologies.
  • Collaboration in a team-oriented, cross-functional environment.
  • Involvement in meaningful projects impacting biopharmaceutical manufacturing.
  • Participation in a positive safety culture promoting health and security.
Full Job Description

The AssociateAutomation Engineer is an integral part of the Oceanside Automation, Data/Digital team within MSAT, supporting the site’s digitalization and data-driven efforts. As a designated Pivotal/Launch site for Phase III and commercial stage products, this large-molecule facility requires an agile individual who is eager to learn, comfortable with ambiguity, and thrives in a collaborative, team-oriented environment.

In this role, you will support daily manufacturing operations and technology transfers by collaborating on automation and data/digital initiatives across various functions. Working with minimal supervision, the successful candidate will assist with qualification protocols, help maintain the validated state of control systems, and contribute to small-scope projects while actively developing their technical capabilities.

The Opportunity

  • Owns and executes small to medium scope automation engineering, data/digital services for existing facility projects, including upgrades, capacity expansions, and equipment replacements.

  • Collaborate with senior engineers to analyze existing manufacturing workflows and suggest data-driven improvements.

  • Support the generation, execution, and review of qualification protocols (Installation, Operational, and Performance Qualification).

  • Participate in drafting and updating GMP Lifecycle Documents (e.g., risk documents, trace matrices, and periodic reviews).

  • Manages and tracks the progress of change records and supporting business process updates with minimal supervision.

  • Collaborate with team members in the start-up, troubleshooting, and real-time floor support of automation and critical process utility systems.

  • Participate actively in site coordination, department, and staff meetings to foster cross-functional alignment.

  • Maintain all mandatory training qualifications and proactively seek opportunities to expand technical knowledge.

  • Support environmental health, safety, and security programs by reporting incidents and fostering a positive safety culture where no one gets hurt.

Who you are

Education and Experience

  • Bachelor’s or Master’s degree in Engineering (Chemical, Computer Science, Electrical or Mechatronics preferred) or a related scientific discipline.

  • 02 years of experience in automation, engineering, or a related technology field.

  • Prior internship, co-op, or academic project experience within a biopharmaceutical, biotechnology, or regulated GMP environment is a plus but not required.

Knowledge, Skills and Abilities

  • Strong desire to learn and adapt to biopharmaceutical manufacturing processes, control systems, and design concepts.

  • Foundational understanding of basic engineering principles, automation, or control theories.

  • Familiarity with foundational programming tools (e.g., Python, GitHub), databases, querying tools, and data visualization concepts.

  • Demonstrated ability to apply engineering principles to solve technical problems independently and make sound decisions under ambiguous conditions.

  • Aptitude and enthusiasm for learning, adapting, and applying emerging digital technologies, including AI/ML tools, to manufacturing data.

  • Ability to learn and comply with cGMP requirements (including gowning, documentation, and compliance procedures) for performing work within a manufacturing facility.

  • Excellent interpersonal skills with a demonstrated ability to collaborate effectively within diverse, multidisciplinary teams.

  • Strong written and verbal communication skills for documenting technical processes and participating in team discussions.

  • Self-motivated with the ability to drive technical deliverables independently with minimal oversight.

Work Environment/Physical Demands/Safety Considerations

  • Work in a standard office environment.

  • May work in the clean room environment that requires gowning in the form of hospital scrubs, coveralls, gloves and steel toe boots. No make-up or jewelry can be worn when working in the clean room environment.

  • May work with hazardous materials and chemicals.

Relocation benefits are not available for this posting

The expected salary range for this position based on the primary location of California is $61,600 - $114,400. 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.

About Genentech

Genentech is a biotechnology company that develops and manufactures drugs for the treatment of serious medical conditions. The company was founded in 1976 and is headquartered in South San Francisco, California. Genentech's products include treatments for cancer, multiple sclerosis, and other diseases. The company is a subsidiary of Roche, a Swiss pharmaceutical company. Genentech has been recognized for its innovative research and development, and has received numerous awards for its contributions to the biotechnology industry.
Learn more about Genentech
Size
14,000 employees
Industry
Founded
1976

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