GILEAD

Sr Facilities Engineer III

United States - California - Foster City Full time

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
 

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.
 

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Job Description
 

Essential Duties and Job Functions: 

We are seeking a highly skilled Senior Automation Engineer to support Biologics technical development, clinical, and manufacturing facilities.

Key Responsibilities

  • Lead the design, development, deployment, and lifecycle management of automation solutions using Emerson DeltaV DCS, with emphasis on batch control (S88), recipe management, and phase logic execution.
  • Support PI Historian system for real-time and historical data collection, trending, Asset Framework creation, and analysis for process monitoring and continuous improvement.
  • Integrate biologics laboratory, pilot, clinical, and manufacturing equipment/systems via APIs, OPC UA, and other protocols to ensure seamless data flow across R&D, clinical, and GMP environments.
  • Support integration of DCS / Historian with MES platforms.
  • Implement and manage automation changes in GMP environments, including hardware/software upgrades, vendor coordination, change control, and qualification/validation activities.
  • Manage external contractors and third-party integrators, including scope definition, performance monitoring, deliverable review, and budget/schedule oversight.
  • Provide technical mentorship and guidance to junior automation engineers.
  • Collaborate with cross-functional teams (Technical Development, Manufacturing, QA, QC, IT) to deliver automation projects that meet cost, quality, timeline, and regulatory goals.
  • Maintain comprehensive, compliant automation documentation (URS, FS, DS, SOPs, risk assessments, validation protocols).
  • Lead validation and qualification efforts in collaboration with QA to ensure adherence to GAMP 5, 21 CFR Part 11, and Annex 11 requirements.

Required Knowledge, Experience, and Skills

  • Extensive hands-on experience with Emerson DeltaV DCS, including configuration of batch control, control/equipment modules, and phase logic.
  • Proficiency in industrial protocols (OPC UA, Modbus, Ethernet/IP).
  • Strong expertise in Aveva PI System (PI Adapters/interfaces, PI Data Archive, PI AF, PI Vision).
  • Experience integrating DCS or Historian with MES (e.g., Apprentice Tempo MES or Werum PAS-X).
  • Proven background in GMP automation within biologics, cell/gene therapy, or large-molecule manufacturing.
  • Demonstrated experience managing contractors and system integrators.
  • Track record of mentoring junior engineers and fostering a collaborative team environment.
  • Ability to rapidly learn and adopt new automation platforms, Cloud Services, and DevOps tools (e.g., Ignition SCADA, MQTT/Sparkplug, GitHub).
  • Strong troubleshooting and problem-solving skills; structured approach to root-cause analysis.
  • Excellent communication and stakeholder management skills; ability to present complex concepts to technical and non-technical audiences.
  • Must be able to work onsite at least 3 days per week.

Basic Qualifications

  • BS in Computer Science, Electrical, Chemical, or Mechanical Engineering from an accredited university with at least 10 years of relevant automation engineering experience in life sciences.

OR

  • MS in Computer Science, Electrical, Chemical, or Mechanical Engineering from an accredited university with at least 10 years of relevant automation engineering experience in life sciences.

Preferred Qualifications

  • Proficiency in PLC (Rockwell, Siemens, Opto22) and SCADA platforms (Ignition).
  • Programming experience in Python or .NET for automation scripting and API integration.
  • Experience with AWS cloud services (EC2, S3, Lambda, RDS, IoT Core) and DevOps tools (Git, CI/CD pipelines, Terraform, Ansible).


 

The salary range for this position is: $182,070.00 - $235,620.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.


For jobs in the United States:

Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance.


For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster.

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Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the  legal duty to furnish information; or (d) otherwise protected by law.
 

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.


Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.


For Current Gilead Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.