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Manager, Global Distribution Quality

at Incyte Corporation in Wilmington, Delaware, United States

Job Description

Overview   Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients, make a difference in health care, and build sustainable value. The Company strives to discover and develop first-in-class and best-in-class medicines-advancing a diverse portfolio of large and small molecules. Job Summary(Primary function) This position will provide support to the Global Distribution team in the area of Packaging & Distribution for Incyte Corporation.This individual will be responsible for complying with the quality requirements and standards for small and large molecule commercial products in a GMP regulated environment. This position will support quality systems and procedures in alignment with the global quality policies and applicable regulations for Incyte's contract manufactures and distribution partners.This role will provide prompt support and guidance to patient's inquiries and facilitate cross-functional activities to resolve issues related to Quality systems, manufacturing/packaging, distribution, and post market surveillance related to Incyte products.The person in this role will continuously inform and improve the systems process while effectively working with cross-functional teams.Strong interpersonal skills are required to be successful in this position. Essential Functions of the Job(Key responsibilities) *Manage the Incyte Distribution network in line with regional scope. *Provide the QA expertise and input for the conduct of Distribution Risk assessments in the assigned regions.Escalate the potential strategic risk through the GMP GDP Risk Management program and the MRB process. *Record, assess and reconcile Product Quality Complaints while coordinate collection of additional information from external and internal stakeholders (i.e. patient, Pharmacies, etc). *Develop, negotiate and maintain Quality Agreements in the assigned territories. *Ensure compliance of Incyte Products by reviewing, approving and ensuring maintenance of Packaging & Shipment Specifications with new product introduction and product expansion. *Develop, maintain and roll-out SOPs in line with scope of activities. *Lead the resolution of Packaging & Distribution related change controls, CAPAs, deviations and logistic events. *Lead Risk Management initiatives for the Distribution Network related to expansion of Incyte products. *Develop and maintain a QA KPI dashboard for Packaging CMOs and Distribution. *Lead the QA part in Quality Business Reviews performed with key 3PLs/Distributors and Partners. *Chair Management Review Board for major and critical product distribution issues for assigned product(s). *Coordinate complaint with Contract Manufacturers to ensure on-time closures of change controls, CAPAs & deviations. *Complete review and approval of packaging component artworks and proofs review for existing and new product introductions for responsible markets. *Cooperate with the US Supply Chain, CMC, QC and RA functions in matters relating to commercial Product. *Manage and organize the batch disposition activities across commercial products to ensure compliance and timely supply of products. *Support Annual Product Review issuance for assigned product(s). *Support and lead the execution of mock recalls and continuously improve process as needed. *Ensure on time issuance, assessment and close out of distribution related deviations & logistic events. *Perform all responsibilities in accordance with company policies, procedures, applicable regulations and safety requirements. *Stay current with applicable International Regulations and promote a Quality culture in all interactions both internally across Incyte organization and externally. *Contribute positively to a strong culture of business integrity and ethics. Qualifications (Minimal acceptable level of education, work experience, and competency) *Bachelor's degree, preferably in a scientific discipline, or 5 years' experience in a pharmaceutical and/or biotech industry in Quality-related roles. *Thorough knowledge of cGMP, GDP and global regulatory requirements. *Ability to multitask and work both independently and within multi-disciplinary teams. *Ability to critically appraise and apply GxP knowledge. *Strong verbal and written communications skills. *Strong interpersonal skills for... For full info follow application link.   We appreciate, celebrate, and thrive on one another’s differences and strengths and are proud to be an Equal Opportunity Employer. By valuing diversity of backgrounds and perspectives and prohibiting all forms of harassment, we are able to promote a collaborative and innovative work environment in which everybody can contribute to their fullest potential.  

 

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Job Posting: 1278338

Posted On: Jun 14, 2024

Updated On: Jun 28, 2024

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