Sr. Manufacturing Automation Engineer II - SCADA (GMP/Biotech/Pharma)
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.
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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. Manager, Manufacturing Automation Engineer II - SCADA (GMP/Biotech/Pharma)
We are seeking a highly motivated Senior Automation Engineer to join our Automation Department in support of the operation of our state-of-the-art facility, home to several new sterile manufacturing lines, packaging lines, and product warehouse. In support of our new facility, the Senior Manufacturing Automation Engineer II, under minimal supervision, will be responsible for managing the Automation team in continual infrastructure and control system enhancements, administration and maintenance of physical and virtual servers and automation layer networks, and manufacturing operational support related to supervisory level automation systems. In maintaining these systems, the individual will be responsible for ensuring that all systems are in keeping with the site standards for Automation, including virtualization, IOT/IIOT frameworks, centralized supervisory software, as well as the data integrity and compliance guidelines required of GMP systems.
The automation systems which the individual will be responsible for includes the Process Control System (PCS) and PCS Information Management System (PIMS), which contains FactoryTalk View, FactoryTalk Historian (OSI PI Historian), FactoryTalk Transaction Manager and SQL Reporting, FactoryTalk AssetCentre, Automation Active Directory servers, Remote Desktop Terminal Servers, and more. The PCS also includes interfacing to IT infrastructure and firewalls, and multiple site-wide fiber networks to ensure secure, highly available network communications between the manufacturing equipment and PIMS. As such, this individual will work closely with IT and manufacturing while collaborating with the site's Quality Assurance, Validation, Engineering, Facilities, and other stakeholders.
Additionally, as all systems are interfacing to the GMP network, the individual should be well versed in FDA Code of Federal Regulations Title 21, Part 11, Computer Systems Validation, GAMP, Data Integrity Compliance, and GMP change management procedures. The individual will be expected to use Maximo, TrackWise, and Veeva Vault systems to facilitate development of documentation, standard operating procedures, work orders, and change management records in line with automation system maintenance and enhancements.
Extensive knowledge of control layer hardware and programming (Allen Bradley ControlLogix, Studio 5000) is strongly preferred, but may supplement roles and responsibilities related to the supervisory level software and hardware.
Specific Job Responsibilities
- Administration and maintenance of the automation servers, systems and network devices for process equipment and systems, with key emphasis on data integrity, high reliability, and redundancy.
- Supervising and onboarding automation contractors in support of project implementation and operational troubleshooting.
- Supporting manufacturing operations in areas related to the automation infrastructure and networks, including cross-functional communication and coordination to resolve issues, and providing automation technical expertise for troubleshooting, investigations and training.
- Operational Projects: Developing, planning and implementing automation-based projects and solutions in collaboration with cross-functional teams, including determination and delivery on cost, time and quality to ensure the sustained production (these projects may be new and/or update to existing).
- Optimization and compliance: Responsible for technical optimization of the automation systems, including the revision of automation standards in keeping with current Good Manufacturing Practices and new industry technology and best practices.
- Creation, modification, and maintenance of automation documentation, including automation specification documents (URS, FDS, SDS), SOPs, P&ID, network topology, PFD, wiring diagrams, panel drawings, etc. in a compliant state.
- Leading a team in the development of commissioning protocols and commissioning reports following project implementation.
- Support the validation of automation systems with Validation department and provide technical skills in regard to Computer Systems Validation strategies.
- May participate in audits to include internal, vendors or contract manufacturers.
- Supports and contributes to site continuous improvement initiatives, including compilation of key performance indicators and technical performance metrics.
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 Bachelor's Degree and a minimum of eight (8) years of relevant experience, OR a Master's degree with a minimum of six (6) years of relevant experience.
- 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.
- Experience with Rockwell Software suite: FactoryTalk View, FactoryTalk Historian (OSI PI Historian), FactoryTalk Transaction Manager, FactoryTalk AssetCentre.
- Experience with SQL Database and Reporting
- Experience in PLC and HMI Allen Bradley hardware programming (ControlLogix, PanelViews)
- Experience in biotech or pharmaceuticals industry.
- 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
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
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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 firstname.lastname@example.org for assistance.
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