Senior Specialist - Automation, Boudry Digital Plant

Job content

Working with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more careers.bms.com/working-with-us.CompetencesIntegrated into the Information Management department, the Industrial IT and Automation Specialist provides support to GMP automated System of Boudry Manufacturing Plant implemented and during their implementation.Skills/Knowledge Required

• Engineering educational background preferably in Automation, Bio or Chemical processing.
• Minimum 2 years of experience in a pharmaceutical/biotech environment with computerized systems (Automation, IT).
• Demonstrated hands-on experience with automation systems.
• Knowledge of specific manufacturing systems (Serialization software, Building management System, Room Monitoring System, MES, etc.).
• Good knowledge of Pharma/Biotech Processes, Utilities and HVAC equipment.
• Awareness of Industry 4.0 and related topics.
• Knowledge of IEC 61131, ISA-88 and ISA-95 Standards.
• Good knowledge of SCADA software and PLC (Siemens, Allen-Bradley, iFix, etc). Knowledge of other platforms is an advantage.
• Good knowledge of Computer Networking and Fieldbus.
• Design, configuration, installation, and maintenance of automation software and associated hardware.
• Oversight or participation on all automation aspects of overall automation projects lifecycle (URS, FS, DS, SDS, FAT, SAT, IQ, OQ, PQ and system support as well).
• Develop procedures and maintain proper documentation related to automation systems.
• Troubleshooting skills to recover system critical functionalities
• Understanding of electrical and P&ID standards.
• Familiar with GMAO software and IT Ticketing systems (ServiceNow).
• Awareness of business and enterprise architecture.
• Analyze, interpret data, and make sound technical recommendations on continuous improvements and non-conformance remediation.
• Good knowledge GxP/GAMP/Data Integrity practices/ASTM E2500.
• Ability to handle multiple projects in parallel.
• Excellent analytical and report writing skills.
• Excellent presentation, facilitation, negotiation, collaboration, and communication abilities.
• Capable of working under pressure in a multi-cultural environment, at any level of the hierarchy, effectively with a variety of stakeholders.
• Ability to coach and supervise collaborators.
• Fluent in French and English.

Duties And Responsibilities

• Provide technical support for Manufacturing Operations.
• Create and maintain Automation governance documentation.
• Collaborate with partners and stakeholder such as automation, IT, Manufacturing and QA in order to execute the daily operational activities and maintain the systems in a compliant state.
• Implement corrective actions as defined by the Deviation management or the Change Control Process that can include (but not limited to) automation code changes, review, design document updates & re-approval, SOP updates and trainings.
• Manage Commissioning & Qualification activities (SAT, IQ, OQ) for projects related to automation systems.
• Work independently and supervise the activities of suppliers.
• Contribute positively to a strong culture of business integrity and ethics.
• Act within compliance and legal requirements as well as within company guidelines.

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing CareersWith a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.