Assist with coordinating and facilitating activities associated with supplier management program and support qualification of new and existing suppliers

•   Assist with annual external audit plan with Global Procurement
•   Coordinate, perform, and assist team members with supplier qualification activities
•   Coordinate and maintain Approved Vendor List

Assist and support local, regional, and global departments with their questions/requests relating to suppliers

•   Perform or assist with supplier risk assessment for non-compliance (i.e. FDA WL, etc.) inspection outcome
•   Collaborate with cross-functional groups and complete supplier (re)qualification activities
•   Interface with suppliers for audits (on-site, virtual, hybrid, or document) and requests (re)qualification documentation, as needed
•   Perform supplier (re)qualification audit, as needed
•   Collect and review supplier (re)qualification documentation
•  Prepare supplier (re)qualification reports or assessment/evaluation reports
•  Update and maintain regional (US QA Compliance) supplier tracking databases
•  Update global supplier tracking databases
•  Perform investigative task in KabiTrack for supplier change notification and manage until closure

Assist with coordinating and facilitating activities associated with Regional internal audit program

•   Perform annual risk assessment for annual internal audit plan
•   Assure internal audits are scheduled, conducted, and closed  
•   Participate in internal audit as a Lead or Co-auditor
•   Plan, prepare, and conduct internal audit
•   Collaborate as Lead or Co-auditor with other auditors (Lead or Co-auditor) to draft audit report, review CAPA Plan, and issue audit closure
•   Interface with auditees
•  Update and maintain internal audit tracking database

Assist with coordinating and facilitating activities associated with Quality Agreement

•   Coordinate and manage the update to Global Procurement Quality Agreement database
•   Coordinate and participate in quarterly Global Procurement Quality Agreement review
•   Coordinate and perform regional periodic review of Quality Agreements
•   Coordinate, negotiate, and support supplier Quality Agreement according to defined business relationship with suppliers
•   Coordinate, negotiate, and support inter-company quality agreement according to defined business relationship with other non-FK USA entities
•   Coordinate, negotiate, and collaborate with cross-functional groups and/or suppliers to draft, review, and/or finalize quality agreement
•   Update global and regional Quality Agreement databases

Assist with preparing monthly management review presentation   

• Coordinate monthly supplier data for product APQR as requested from Production Units   
• Assist and perform Implementation Assessment for Instructive Global QM Documents   
• Provide and support Annual Supplier Evaluation   Coordinate and assist team members in supporting internal, external, customer, and regulatory inspection, as needed  
• Support maintenance or process improvement of programs for supplier management, internal audit, and quality agreement, as needed  
• Act as back up in the absence of Senior Manager, with support from VP, NAM Quality  

Requirements

• Must have a Bachelor's degree in the sciences with  8+ years of progressive challenging QA/QC experience in pharmaceutical or related regulated industry.
• Must have an in depth knowledge of current GMP and related quality systems.
• Must possess strong leadership, communication, interpersonal skills, negotiation and problem resolution skills.
• Must be organized, detailed and have ability to handle multiple tasks at once and redirect focus based on company's needs.
• Must be able to function independently with minimal supervision.
• The Company’s primary business language is English. The successful candidate must be able to effectively speak, read, write, and understand English to perform the essential functions of the position, including independently understanding policies, procedures, training materials, and workplace communications written in English due to our heavily regulated work environment.