Contract Manufacturing Sr Mg

Team Horizon is seeking a CW Contract Manufacturing Sr Mg for our client based in Dublin. Hybrid work with onsite requirement once a month.

Why you should apply:

• This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.


• There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.


• Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.

What you will be doing:

• 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.

What you need to apply:

• 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)    


• Assimilates multiple inputs and allocates resources to potentially conflicting priorities     


• Anticipates and resolves complex problems and integrates into continuous improvement