Senior Manager, Third Party Manufacturing

AbbVie is seeking a Senior Manager External Manufacturing to lead the relationship with and
performance of its third-party manufacturers.
In this strategic and operational role you will serve as AbbVies primary point of contact for several
industrial partners. You will directly contribute to ensuring continuity of supply quality regulatory
compliance manufacturing performance and cost competitiveness for externally manufactured
products.
This opportunity is suited to someone who wants to grow within a multicultural organization that
combines agility commitment and speed of execution.

This role can be based in any of our 5 manufacturing sites across Ireland (Cork Dublin Sligo or Westport).

Key responsibilities

• Manage relationships with third-party manufacturers by defining effective governance
  responsibilities operating models and communication channels.
• Ensure continuity of supply by coordinating forecasts production schedules and delivery plans with Supply Chain Planning and industrial partners.
•  Anticipate and manage operational risks related to capacity raw materials components lead times or supplier performance to prevent supply disruptions.
•  Lead governance and operational performance through Virtual Operations Teams (VOTs) business
  reviews and steering committees with third-party manufacturers.
•  Define monitor and improve performance indicators covering quality service cost capacity and
  lead times and coordinate the associated action plans.
•  Drive issue resolution and required escalations preparing reports and executive summaries for
  management.
•  Ensure compliance with quality and regulatory requirements in close collaboration with Quality
  teams and manufacturing partners.
•  Coordinate audits inspections annual quality reviews deviations investigations and CAPAs
  ensuring corrective actions are implemented within expected timelines.
•  Contribute to product release and decision-making regarding potential non-conformities.
•  Lead technology transfers and strategic projects related to external manufacturing process
  changes and manufacturing performance improvement.
•  Coordinate internal teams and industrial partners throughout projects managing risks timelines
  resources costs and communication.
• Support products throughout their lifecycle and identify opportunities to improve reliability
  manufacturing robustness and profitability.

Qualifications :

• Degree in Engineering or a scientific discipline
• Minimum 7 years of experience in the pharmaceutical biotechnology or related regulated industry
• Sterile manufacturing experience (mandatory)
• Aseptic processing experience (mandatory)
• Technology transfer experience (mandatory)
• Strong project management and supplier management skills
• Excellent stakeholder management negotiation and communication capabilities
• GMP and quality systems knowledge

Internal grades may vary depending on country.

Additional Information :

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more visit  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

No

Employment Type :

Full-time