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Sr. Manufacturing Automation Engineer II

Employer
Gilead Sciences, Inc.
Location
Foster City
Salary
See job description.
Closing date
Dec 18, 2020

View more

Discipline
Other, Other
Position Type
Full Time
Job Type
Manager
Organization Type
Pharma


Sr. Manufacturing Automation Engineer II
United States - California - La Verne

Gilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Gileads therapeutic areas of focus include HIV/AIDS, liver diseases, cancer and inflammation, and serious respiratory and cardiovascular conditions.

Making an impact on a global scale
Inclusion is one of the companys five core values. Thats because we know that we are stronger and more innovative at Gilead when we are informed by a diverse set of backgrounds, experiences and points of view. Gilead Sciences is a biopharmaceutical company that discovers, develops and commercializes innovative therapeutics in areas of unmet medical need. The company's mission is to advance the care of patients suffering from life-threatening diseases worldwide.

When you join Gilead, you join our mission to change the world by enabling people to live healthier and more fulfilling lives. Come join a mission-driven bio-pharmaceutical organization that values inclusion and diversity, has a strong portfolio of products, and is constantly #CreatingPossible


Sr. Manufacturing Automation Engineer II

Job Responsibilities
  • Maintain the automation servers, systems and network devices for process equipment and systems
  • Develop and implement strategies for data management and data flow through automation network.
  • Locate and diagnose system failures and perform troubleshooting for automated process equipment and systems
  • Develop solutions to automate manual tasks by implementing upgrades to PLCs, HMIs and SCADA systems
  • Support the high levels of reliability for the Process Control System Information Management and Network Infrastructure
  • Manage the standards, methods and procedures for the design, modification, and maintenance of manufacturing processes.
  • Develop, modify and redline specifications for: mechanical and electrical contractors, equipment, software, hardware, P&ID, network topology, PFD, wiring diagrams, panel drawings, etc.
  • Plans, executes and tracks a variety of engineering projects.
  • Contributes to the development of department strategy.
  • Coordinates cross-functional efforts to resolve manufacturing and maintenance issues in projects and day-to-day operational activities.
  • May participate in audits to include internal, vendors or contract manufacturers.
  • Implements systems for tracking project progress.
  • Supports and contributes to site continuous improvement initiatives.
  • Compiles and reports technical performance metrics.
  • Maintains and develops existing engineering systems which support equipment run times.
  • Develops lifecycle documents including URS, FDS, SDS, FAT, SAT, Commissioning, IQ, OQ, and PQ protocols.


Knowledge & Skills
  • Demonstrates extensive understanding and application of process engineering principles, concepts, practices, and standards.
  • Demonstrates proficiency in current Good Manufacturing Practices (GMPs), 21 CFR Part 11/Annex 11, regulatory compliance, strategic planning, data management, and safety regulations.
  • Demonstrates knowledge of pharmaceutical process manufacturing, OEE, MTBF, and root cause failure analysis.
  • Demonstrates excellent verbal, written, and interpersonal communication skills.
  • Proficient in Microsoft Office applications


Education & Experience
  • A minimum of eight (8) years of relevant experience, and a BS or BA or related fields.
  • A minimum of six (6) years of relevant experience, and a MA or MBA.
  • Has experience with automated infrastructure that include: security strategies, network architecture, platform selection and full implementation of 21 CFR Part 11 and EU annex 11 requirements
  • Has extensive experience in PLC-based programming (e.g. Rockwell software)
  • Has previous experience with developing Audit, Event, and Batch reports and integrated into centralized reporting system.
  • Has previous experience in biotech or pharmaceuticals industry.
  • Has previous experience in engineering in highly-regulated manufacturing environments.


If this is not the right move for you now but remain interested in a career at Gilead Sciences please connect with us via our talent community: https://gilead.avature.net/Gilead

About Gilead

Gilead Sciences, Inc. is a research-based biopharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Gilead's therapeutic areas of focus include HIV/AIDS, liver diseases, cancer and inflammation, and serious respiratory and cardiovascular conditions.


For jobs in the United States:

As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, 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 careers@gilead.com for assistance.

For more information about equal employment opportunity protections, please view the EEO is the Law' poster.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

PAY TRANSPARENCY NONDISCRIMINATION PROVISION

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 log onto your Internal Career Site to apply for this job.


To apply, visit https://gilead.wd1.myworkdayjobs.com/en-US/gileadcareers/job/United-States---California---La-Verne/Sr-Manufacturing-Automation-Engineer-II_R0015024-2





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