Senior Manufacturing Scientist, (OSD operations)

Conteúdo do emprego

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.Fixed Term Contract : End Date 31.03.2026TheSenior Scientist has the responsibility to lead and deliver, with the support of an external engineering firm, process equipment packages (i.e. tablet laser marking, excipient dispensing, IBC & parts washing machine, IPC isolators for containment purpose) for a new Oral Solid Dosage (OSD) manufacturing site located in Boudry, Switzerland. This process starts from defining system requirements, selecting the vendor, performing detailed design activities with each equipment vendor, attending Factory Acceptance Testing (FAT) up to end of equipment qualification.In this role, will be part of the project team that supports the construction of a new manufacturing facility P3, which aims to be a center of excellence for OSD drug product manufacturing for BMS.Skills/Knowledge Required

• Minimum of bachelor’s degree in science or engineering discipline (chemistry, pharmacy, biology, chemical engineering or a related pharmaceutical science).
• At least 5 years’ experience in pharmaceutical development or production.
• Must have a good working knowledge of QA, cGMP and the Pharmaceutical Regulatory framework.
• Good knowledge of various types pharmaceutical Manufacturing processes/technologies. Experience in OSD operations would be an asset for the project.
• Demonstrated project leadership/management experience.
• Experience in working in close collaboration with equipment vendors, managing deliverables and associated schedule.
• Excellent technical/scientific skills and knowledge (knowledge of key pharmaceutical unit operations).
• Strong communication skills, good interpersonal skills, ability to multi-task, publication track record and a strong desire to learn, contribute and collaborate.
• Excellent leadership skills and ability to influence and work across organizational boundaries.
• Excellent command of English and preferably French language.
• Ability to work well as an integral part of a large Project Team.

Duties And Responsibilities

• Lead simultaneously several unit operations packages from vendor selection process to closure of equipment qualification activities.
• Own and lead system requirements definition for each technology, ensuring alignment with BMS network (Product Development, MS&T, Manufacturing and Clinical Manufacturing Site) and in full compliance with BMS standards. This will enable a seamless and robust process technical transfer from development to Boudry commercial manufacturing site.
• Advocate best practice project methodologies and tools. Develop, write and/or review project documentation including system requirements, drawings, test protocols, risk assessments and reports.
• Provide technical/scientific expertise and support the Engineering firm during technical discussion with equipment vendors meeting.
• Accountable for budget management and the delivery of each unit operation package in line with project schedule and system requirements defined.
• Ensure alignment of equipment selection process and the definition of CQA’s and CPP’s as basis for the control strategy.

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 cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.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.