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Senior Manager Contract Manufacturing

Posted 8 hours 56 minutes ago by Morgan McKinley

Permanent
Full Time
Other
Dublin, Dublin, Ireland
Job Description

Contract Manufacturing Senior Manager (Site Lead) - 1 day per month onsite - 12 month contract

Responsibilities:

Manufacturing operations: Develop and lead robust business processes, maintain reliable relationships with contract site management; assess industry trends, internal network, and technology advancements as tools to improve contract site performance. Manage budget development, monitoring, and reporting; create and manage contracts - confidentiality disclosure agreement(s), scope of work agreement(s), request for pricing/information, supply agreement(s) etc.; monitor and improve financials with CMO; actively manage and communicate forecasts to the sites and manage capacity planning. Drive operational excellence and champion change.

Site performance monitoring: Manage contract site performance using lean tools and PDCA, lead site operating review meetings; drive improvements at contract sites; sustain and improve the overall health of the business, and lead communication/relationship with the contract site as well as internal management.

Project Management and Technology transfer: Lead a department-wide project from conception to implementation and close-out. Present to and obtain buy-in for value proposition of such projects to senior management. Provide oversight of all planning and coordination of product transfer activities to the contract site(s); develop, present, and obtain approval of budget, timeline and ensure execution of transfer team activities to achieve seamless product transfer to the contract site(s); ensure risk management initiatives are taking place as per RM plan; lead site issue management and resolution; provide issue escalation to executive management.

Preferred Qualifications:
  • Bachelor's in Business Administration, Engineering, or Science-related field
  • 8+ years of experience in protein, API, DS, DP, or packaging manufacturing environment
  • 8+ years in roles requiring knowledge of cGMP principles, FDA and other regulatory guidelines, and validation principles
  • 5+ years of experience working with external parties and/or leading cross-functional teams for clinical and/or commercial products
  • 3+ years of project management experience leading multi-functional and multi-location team
  • 3+ years of experience across ACM or CMQ
  • Ability to travel +/- 20% of time (domestic and international)
Competencies:
  • Assimilates multiple inputs and allocates resources to potentially conflicting priorities
  • Anticipates and resolves complex problems and integrates into continuous improvement
  • Establishes and manages business budget
  • Strong influence and negotiation skills
  • Expertise in problem solving and risk-based decision-making
  • Demonstrated matrix management and organizationally savvy
  • Promotes and drives organizational change
  • Excellent project management skills
  • Mastery of contractual requirements
  • Demonstrated ability to lead effectively in collaborative/team environment
  • Demonstrated ability to take initiative, drive action, and works independently
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