Associate Specialist Manufacturing Process Excellence position at Bristol Myers Squibb.| Switzerland

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Bristol Myers Squibb Associate Specialist Manufacturing Process Excellence

Experience: 2-years

Pattern: Full time

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Associate

Boudry - CH....Switzerland

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Working with Us Challenging. 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. 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 . Supports manufacturing process documentation, equipment commissioning and troubleshooting, and continuous improvement initiatives. This position focuses on writing technical documentation, participating in equipment qualification activities, and ensuring timely closure of quality records. Duties/Responsibilities Provide Expertise in manufacturing processes Write technical documentation Participate in the Commissioning, FAT/SAT, IOQ, PQ and Operational Readiness as part of new equipment Write System requirement definition & associated supporting quality records and documentation (e.g.change management,…) to support equipment enhancement post product commercialization or Manufacturing process Support Data Integrity risk assessment Prepare and assist Operations teams with new equipment set up and troubleshooting Participate in equipment qualification tasks. Deploy , maintain & execute level 1 maintenance Act as primary point of contact for equipment troubleshooting Write LO/TO documentation (e.g ECP) Participate in A3 problem solving initiatives related to technical topics Own & lead local continuous improvement initiatives. Provides technical expertise for investigation, CAPAs, Process improvement and in other various topics upon request Ensure on-time closure of quality records (e.g.CAPA, Action, document periodic review,..) Own and lead change control at the discretion of the production team This job description is not intended to be exhaustive; additional duties and responsibilities may be assigned as needed to meet business requirements. Qualifications Bachelor’s degree or equivalent in technical discipline. 0–2 years of experience in pharmaceutical operations. Understanding of GMP and technical processes. Proficiency in French (mandatory) and English. 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 Careers With 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 a supportive culture, promoting global participation 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 Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. Supporting People with Disabilities 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. Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection . Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley. R1601990 : Associate Specialist Manufacturing Process Excellence

Associate Specialist Manufacturing Process Excellence job opportunity at Bristol Myers Squibb.

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