Associate Director, Supply Chain Product Leader

Cudrefin, Waadt, Switzerland

Job Description

\\n Working with Us
Challenging. Meaningful. Life-changing. Those aren\\xe2\\x80\\x99t 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\\xe2\\x80\\x99ll 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: .

At Bristol Myers Squibb, we are inspired by a single vision \\xe2\\x80\\x93 transforming patients\\xe2\\x80\\x99 lives through science. In oncology, hematology, immunology and cardiovascular disease \\xe2\\x80\\x93 and one of the most diverse and promising pipelines in the industry \\xe2\\x80\\x93 each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

Position Summary:

Responsible for all Supply Chain activities required to support a brand/brands:

Supply Chain Representative of the Global Operations Team (GO-Team) and with the responsibility to integrate the product supply strategy into the cross functional Supply Chain Sub Team.

Lead all Supply Chain processes including interface with Supply and Demand planning, Inventory Management, Business Continuity and Market Supply Operations.

Facilitate Cross-functional engagement within GPS and between GPS, Regulatory, Finance, Quality, MS&T and Alliance Management (as applicable).

Key Responsibilities:

Represent Global Supply Chain on product focused at Global Operations Team (GO-Team) and Regulatory & Supply Team (RST); lead the SC sub-team to drive brand Supply Chain performance

Develop annual E2E Product Supply Strategy (including inventory, sourcing strategies, logistics and business continuity)

Own & drive E2E value stream map improvements related to supply chain activities (training and processes)

Maintain regulatory and supply strategy (in partnership with Regulatory Lead) and supporting material control strategy (in partnership with Quality Product Lead)

Support GSR (responsible to escalate brand-level exceptions) and market S&OP (responsible to cascade down brand strategy)

Ensure Alliance Management and business partners aligned to brand strategy

Create strategic \\xe2\\x80\\x98what-if\\xe2\\x80\\x99 scenarios to proactively identify risks and opportunities

Engaging with Long-term Planning for sourcing strategies

Endorse product scenario analysis from the Planning Team \\xe2\\x80\\x93 confirm manufacturing plan is aligned to supply and demand requirements

Develop strategies to manage supply fragmentation

Lead resolution of escalated global supply risks (through Allocation)

Assess Supply Chain Management impact during Change Management execution for process changes

Qualifications & Experience:

If you come across a role that intrigues you but doesn\\xe2\\x80\\x99t 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.

Undergraduate Degree preferably in Supply Chain Management, Engineering, or Life Sciences

Advanced degree, diploma or certification in Supply Chain Management, Engineering, or MBA preferred

10+ years of related experience in supply chain or manufacturing in a pharmaceutical environment.

Knowledge of/exposure to world class planning and execution processes and preferably supported by ERP and Advanced Planning Systems (preferably SAP suites).

Minimum of 3 years of experience as a leader of cross-functional teams and/or managing staff.

Experience in pharmaceutical manufacturing and supply chain highly preferred

Good understanding and exposure to current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA) and other regulatory requirements (EMA, TGA).

Experience in working internationally in a fast-paced, reputed, global pharmaceutical/Biotechnology or Consumer company organized in a matrix structure

Experience in developing and implementing world class, global supply chain planning processes and managing them through deployment of global advanced planning and scheduling systems

Additional professional and personal requirements include:

Business Acumen: Has a strong understanding of the key business drivers of the industry/organization. Persuades others with fact-based judgments of the business situation.

Setting Strategy: Makes decisions that balance a variety of factors (e.g., quality, cost, risk, short-term v. long-term impact, etc.). Sets a clear direction for others in times of uncertainty and change. Constructively challenges the conventional wisdom or accepted ways of doing things.

Executing for Results: Maintains high standards of performance for himself/herself and others, and follows through on commitments. Demonstrates integrity, and sticks to core values and principles. Takes the long view, and when faced with challenging obstacles, persists over a significant period of time to achieve his/her agenda. Conveys a sense of urgency, and drives issues to closure. Makes timely decisions when a quick response is required and a number of possible alternatives are available.

Leading Teams: Holds people accountable for agreed-to results. Identifies and keeps others focused on the most important metrics to drive the business. Forges strong, diverse teams of people with multiple perspectives and talents. Includes direct reports and key stakeholders in setting goals, developing plans and making decisions to build commitment and create alignment. Is a strong mentor and builds organizations of effective leaders.

Building Relationships and Using Influence: Establishes credibility and earns respect with a diverse set of internal and external stakeholders including senior executives, manufacturing and other functional leaders, regulatory professionals, contractors and other partners. Is highly articulate, and makes arguments in a clear and compelling manner. Is able to \\xe2\\x80\\x9cget things done\\xe2\\x80\\x9d without compromising principles. Has excellent negotiating skills and achieves win-win outcomes in difficult situations.

Why You Should Apply

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or any part of the recruitment process direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.

#LI-Hybrid

If you come across a role that intrigues you but doesn\\xe2\\x80\\x99t 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 \\xe2\\x80\\x9cTransforming patients\\xe2\\x80\\x99 lives through science\\xe2\\x84\\xa2 \\xe2\\x80\\x9d, 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
Physical 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 . Visit 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.\\n \\n \\n \\n \\n \\n

\\n\\n Bristol-Myers Squibb\\n \\n\\n

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Job Detail

  • Job Id
    JD1602438
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Cudrefin, Waadt, Switzerland
  • Education
    Not mentioned