Senior manufacturing scientist

Senior Manufacturing Scientist 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 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.
Fixed term Contract - 12 months
MS&T is a science-driven organization dedicated to building in-depth and comprehensive knowledge of our products and their processes. We work across the entire lifecycle of our Pharmaceutical Products and support the Boudry internal manufacturing site.
The Manufacturing Scientist / Senior Manufacturing Scientist leads with the support of an external engineering firm, WIP / CIP process development for a new Oral Solid Dosage (OSD) manufacturing site located in Boudry, Switzerland. Supports system owners as required to ensure projects are delivered within agreed timelines, cost and quality targets. Performs detailed design activities with each equipment vendor, attends Factory Acceptance Testing (FAT) up to end of equipment qualification. Provides technical expertise to improve capacity, quality, cost or to establish root cause.
Duties/Responsibilities
Lead/manage simultaneously the development, implementation, and qualification of WIP / CIP cycles for multiple washing skids linked to multiple unit operations in a solid oral dosage manufacturing facility.
Support system owners during installation, qualification, and turn over processes of systems to ensure their proper functioning and installation.
Support verification of system requirements for each technology, ensuring alignment with BMS network (product development and clinical manufacturing site) and in full compliance with BMS standards.
Advocate best practice project methodologies and tools. Develop, write and/or review project documentation including system requirements, drawings, test protocols, risk assessments, reports, qualification documents, and turn over packages.
Responsible to provide support to system owners in the qualification, management, and delivery of each system package in line with project schedule and system requirements defined.
Provide technical/scientific expertise and support the engineering firm during technical discussion with equipment vendors meeting.
Active participation in the design, execution and data analysis associated.
Advise on the definition of CQA’s and CPP’s and an appropriate control strategy.
Responsible for expanding and continuously updating a scientific knowledge base. Advises on Scientific and Business developments (including Technology, Processes, Regulations etc).
Applies and advocates the use of QbD, Lean and 6 Sigma methodologies.
Assist with the development of Standards, guidelines and SOP’s to enhance the quality and robustness of our manufacturing operations, knowledge transfer and technical support processes.
Qualifications
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.
Demonstrated project leadership/management experience.
Good knowledge of various types pharmaceutical Manufacturing processes/technologies.
Experience in working in close collaboration with equipment vendors, managing deliverables and associated schedule.
Excellent leadership skills and ability to influence and work across organizational boundaries.
Ability to work well as an integral part of a large Project Team.
Excellent command of English and other European language.
Travel: This position may require travels at vendors facilities for design review and technical trials.
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.
On-site Protocol
BMS has a diverse 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.
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.
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.

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