Ex. Director, Global Supply Chain Security and - Morges, Schweiz - Incyte Corporation

Incyte Corporation

Geprüftes Unternehmen

Morges, Schweiz

vor 1 Woche

Geschrieben von:

Lena Schneider

beBee Recruiter

Beschreibung

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

Anticounterfeiting 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 anticounterfeiting 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 anticounterfeiting 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 35 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 multidisciplined decisionmaking 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.

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