Ex. Director, Global Supply Chain Security and

vor 6 Monaten

Morges, Schweiz Incyte Corporation Vollzeit

SUMMARY

The Executive Director is responsible for the overall supervision of Incyte supply chain security and anti-counterfeiting program, applicable to all commercial products (large and small molecules one).

The incumbent will oversee, manage and coordinate internal and external activities; communicate and work with several partners and functions; establish and implement the supply chain security and anti-counterfeiting strategy and operationalize the necessary measures to ensure Incyte, its products and its patients are safeguarded.

The incumbent is responsible to ensure that at any time and location, patients will constantly receive genuine product, manufactured and supplied by approved and official entities and/or partners.

DUTIES AND RESPONSABILITIES
- Anti-counterfeiting features
- In charge of the features’ definition to be implemented for each commercial product and supplied regions (i.e. over and covert features)
- In charge to define, implement the methodology on how to manage them (control, life cycle of every features)
- Coordinate the implementation and life cycle of these features with internal and external partners
- Supply chain security
- In charge to define and implement the necessary program, to validate and control the integrity of our different supply chain, including internal and external manufacturing and packaging sites, warehouse, transport, distribution centers
- In charge of implementing this program to Incyte internal entities and external partners
- In charge of conducting or participating to audits, with QA, to verify partners compliance to the defined guidelines, including destruction
- Governance
- Member of Incyte’ s the Management Review Board (MRB)
- Chairing Incyte’ s Falsified Drug Product Committee (FDPC)
- Interface with internal functions and external partners (i.e. authorities, communications, etc.)
- In charge of the definition of the governance model:

- Forum, Metrics, information, communication tools, frequency
- Close communication the Incyte Senior Management
- Forum Participation
- In charge of identifying and participating to key Supply chain security - anti-counterfeiting forum
- In charge of ensuring that Incyte voice will be taken into consideration for any rules, law changes
- In charge of keeping Incyte up to date for any new guideline, recommendation
- Investigation
- In charge of the investigation work in case of a falsified product confirmation, in close collaboration with Incyte Legal
- In charge of coordinating the investigation activities of the Incyte Entities and External at the country level (where falsified product has been identified)
- In charge of purchasing suspected product, in close collaboration with Incyte Legal
- IP protection and Monitoring
- Collaborate and support Incyte Legal’ s Brand Protection activities related to Incyte’ s anti-counterfeiting program
- Consolidate and Report such activities l to relevant internal forums (e.g. FDPC)
- Enforcement
- Collaborate, support the legal work
- Others
- Responsible for establishing the Supply Chain security and Anti Counterfeit Product (ACP) strategy, propose enhancements and operationalize them
- Oversee all work streams and ensure activities are deliver on time
- Act as the primary Global Technical Operations business point of contact for supply chain security and ACP program at Incyte
- Contribute positively to a strong culture of business integrity and ethics
- Act within compliance and legal requirements as well as within company guidelines
- Define a yearly budget to support the SC security and ACP program and monitor actuals vs. budget

**REQUIREMENTS**:

- BS or MS in science or medically related fields
- Highly knowledgeable of regulatory requirements and enforcement, especially ICH/GMP
- At least 12 years manufacturing, supply experience in a pharmaceutical company with additional 3-5 years Quality experience in a pharmaceutical company or other related activity
- Broad knowledge of Pharmaceutical Quality, Manufacturing, supply and GLP/GCP/GMP practices;
- Leadership, ability to build trust and create collaborative environment and relationships;
- Understands the business agendas and perspectives of others; recognizes and effectively balance the interest and needs within the organization;
- Strategic thinker who can balance near term objectives with long term goals and outcomes. Evaluate risks and develop effective solutions through an integrated multi-disciplined decision-making approach.
- Continuous improvement and critical thinking mindset
- Successful experience in managing diverse virtual teams and be able to navigate & working in a matrix environment
- Excellent verbal & written communication skills
- Superior ability to explain complex issues in simple terms and adapt tone for different users
- Travel ~10%

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are n

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