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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. Read more: careers.bms.com/working-with-us .

The Manager Bulk project ad Operations has the responsibilities to support the Oral Solid Dosage (OSD) manufacturing group within routine activities and projects.

He/She is also accountable for project execution and acts as an SME for small to major CAPEX project.

Manufacturing project includes New Product Introduction (Capsules/Tablets), Technology Transfer, Implementation or Modification of Manufacturing equipment as well as Continuous improvement of manufacturing processes in term of efficiency, safety and compliance.

He/She is responsible of deliverables to meet Projects milestones as well as bringing leadership and expertise in the team while taking into consideration the company's commitment to our Core Values and Behaviors.

The Manager Bulk project & Operations acts as deputy of the Head of Bulk Operations.

• Be Subject Matter Expert in Bulk OSD manufacturing for the introduction of new products, Technology Transfer, Process/equipment validation.

• Define and set the strategic objectives for Bulk project and provide periodic reporting Leadership Team Management.

• Communicate pro-actively, consistently and coordinate with the different stakeholders and with the members of the local management team to meet Bulk project objectives.

• Act as Change Owner and/or evaluate technical changes, define, and monitor the implementation of actions.

• Technical author and approver for operating procedures, including protocols & reports.

• Expertise in the use of process automation system SAP, MES, Equipment Human/Machine Interface (HMI).

• Participate in the drafting of System requirement

• Participate in the Commissioning, FAT/SAT, IOQ, PQ and Operational Readiness as part of new equipment.

• Provides technical expertise and leadership for investigation, CAPAs, Process improvement.

• Evaluates process performance, reports variances to management with recommendations for process enhancement.

• Organized and rigorous, able to provide leadership and coaching to the team

• Natural leader, at ease to take autonomously important decisions under pressure and to drive successful execution, aptitude to work on the floor.

• Exceptional problem-solving ability. Drives Continuous improvement to sustain and enhance efficiency, safety and compliance within manufacturing operations.

• Participate in the review and approval of the Risk Assessments (Process & Data integrity)

• Ensure high standard of training is delivered to the manufacturing teams as part of Manufacturing project deployment.

• Role model of BMS Behaviors and Safety culture

• Act as a Deputy for head of Bulk Operations

Qualifications

• Degree in Science or Technology

• 10 years of experience in pharmaceutical industry in Bulk operations (OSD preferred).

• Knowledge of the GMP environment and pharmaceutical industry, especially in the Bulk OSD (Capsules & Tablets form) including the operation of production machines. Could manage a project with multiple stakeholders.

• Excellent knowledge of the stages of launching new molecules and innovative OSD Bulk Manufacturing techniques.

• Fluent in French and C1 in English.

• Be versatile, organized, rigorous and a good communicator with excellent interpersonal skills for teamwork.

• Excellent leadership skills.

• Share expertise, technical knowledge and experience with others in order to develop your team.

• Knowledge of basic computer tools (Word, Excel, Powerpoint), knowing how to use them as a support during presentations.

• Be force of proposal in the organization of work and know how to implement improvements using Lean tools.

• Communicate the progress of activities and any problems encountered.

• Set up continuous improvement projects by using problem analysis toolkit in collaboration with the support departments.

• Have a sense of responsibility.

• Deliver presentations to a group of people.

• Good knowledge of different packaging processes.

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 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 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:

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.

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/ (https://careers.bms.com/eeo-accessibility) 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.

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/

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Company: Bristol-Myers Squibb

Req Number: R1587681

Updated: 2024-12-17 05:25:16.625 UTC

Location: Boudry-CH

Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.