Director, Global Product Supply, Packaging Strategic Sourcing

Boudry, Neuenburg, 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: .

The purpose of the Director, Packaging Strategic Sourcing role will be to partner with key business leaders and lead our packaging and devices strategic sourcing team to ensure BMS packaging and devices supply base meets the needs of the business including the following:

Enable packaging and devices category strategies that meet the needs of the Global Manufacturing business unit (internal and external manufacturing), and deliver quality, cost, and supply as defined by the business need.

Simplify our procurement processes to enable speed and responsiveness to the needs of external manufacturing.

Actively and proactively manage the risks and develop risk mitigation plans for risks identified in partnership with the business unit.

Major Responsibilities and Accountabilities:

Inspire, develop, and enable a Packaging and Devices Category Strategy that contemplates cost, risk mitigation, supply assurance, quality, supplier diversity, innovation, and supplier segmentation approach that generates significant enterprise value over the next 3-5 years.

Partner with cross-functional leaders in MS&T, Quality, Operations, and Finance to develop, sponsor, and execute Packaging and Devices process and governance improvement that is effective, efficient, and aligned around the value enablement program for enablement of improved supply assurance, risk management, quality performance, cost efficiency, and all other value drivers.

Ensure Category sub-plans are aligned and enable the Packaging and Devices Category strategy value creation plans with the cost, quality, risk, and innovation needs the business will enable.

Partner closely with Supplier Performance & Development and Business Continuity Management teams to insure that risk is assessed and managed appropriate according to the needs of the business and in compliance with corporate policies.

Support key, escalated direct negotiations as appropriate.

Coordinate, review, and drive core Strategic Sourcing & Procurement (SS&P) cadence deliverables for packaging and devices category areas including projections, budget and standard costs, opportunity assessments, Procurement Risk Assessment & Mitigation (PRAM) refresh, and regional procurement strategy refresh

Develop and lead diverse team of Sourcing professionals and partner with HR business partners and talent acquisition team to ensure robust talent pipeline to minimize support interruption.

Own Packaging and Devices Sourcing multiyear productivity plans to ensure maximum total value enablement to the needs of the business.\\xe2\\x80\\x8b

Qualifications

Minimum Requirements

Minimum education of an Bachelors Degree preferably in Supply Chain Management, Engineering, or Life Sciences. Advanced degree, or certification in Supply Chain Management, Engineering, or MBA strongly preferred

Minimum of ten (10) plus years of related experience with at least 4 of those years managing Sourcing or External Manufacturing Procurement for a reputable, global Pharmaceutical Biologics, or similar company.

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

Experience in working internationally in a fast-paced, reputed, global pharmaceutical/Bio-Technology company organized in a matrix structure

Knowledge of/exposure to cGMP requirements, research and development, and world class planning and execution processes

Experience in developing and implementing world class, global sourcing or procurement processes and managing them through deployment of electronic tools such as Ariba or SAP

Preferred Qualifications

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

#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

\\n

Beware of fraud agents! do not pay money to get a job

MNCJobs.ch will not be responsible for any payment made to a third-party. All Terms of Use are applicable.


Job Detail

  • Job Id
    JD1603753
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Boudry, Neuenburg, Switzerland
  • Education
    Not mentioned