Cache of job #14166771

Job Title

Senior Manager, Global R&D

Employer

CPL

Location

Limerick

Description

On behalf of our Medical Devices Client in Limerick, we are currently sourcing a Senior Global R&D Manager to join their Team. This position is an 18-month contract role. Responsibilities: ·      Plans, organises, communicates and executes multiple projects to meet the demands of the Divisional program strategy. ·      Collaborates in program planning process ensuring Divisional objectives are met by efficient use of budget and resources. ·      Work to develop plans to address issues and minimize risk associated with the program / individual projects. ·      Manages and reports on program cost / budget. ·      Works to ensure sharing of R&D best practice and resource alignment. ·      Ensures the implementation established processes for the communication of project / program progress. ·      Works in preparation, structuring and facilitation of program decision meetings and other leadership forums in which strategic product development investment decisions are made. ·      Facilitate use of global project management tools. ·      Ensure R&D KPI’s and business metrics are achieved. ·      Fosters relationships and collaborates with other functional stakeholders required for the successful implementation of the program. ·      Foster and maintain a workplace culture respectful and supportive of individual differences. ·      Must ensure the development of personnel within the program and broader R&D function. ·      Must work and interact effectively and professionally with and for others throughout various levels of the global organization. ·      Must have effective negotiation skills. ·      Must maintain company quality and quantity standards. Qualifications / Requirements: ·      Bachelor’s degree is required; Engineering or Science discipline is strongly preferred. ·      A minimum of 7 years R&D and project management experience with experience of managing multiple projects concurrently. ·      Experience working in a Global environment across many cultures and regions. ·      Experience in project, program and portfolio management in a complex new product development environment. ·      Good working knowledge of medical device quality & regulatory systems and medical device directives (ISO13485 and FDA CFR 820), EU Medical Device Regulation 2017/745. ·      Must have effective oral and written communication skills. ·      Excellent analytical and problem solving skills  ·      Ability to remain calm and receptive in fast paced situations. ·      Highly effective goal-setting and implementation skills. ·      Willingness and availability to travel on company business (approx. 20%) You must have the right to work in Ireland for this role. I f you have the above skills & experience, please contact catriona.duggan@cpl.ie / Tele: 087 2419644.

Date Added

487 days ago

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