Loading...
 
Share this Job
Apply now »

Title:  Program Manager, R&D

Requisition ID:  41825
Date:  Nov 27, 2021
Location: 

Dublin, Leinster, IE

Department:  R&D
Description: 

 

 

Working at West means having an opportunity to work by the side of our patients and customers, our global team members and the communities in which we operate – which all help contribute to a Healthier World.

 

At West, we are by the side of patients. The work we do impacts patients’ lives each and every day – our products are a critical part of healthcare delivery and we are proud of the role we play to improve patient health. We work by the side of our team members. We come together as one global team to deliver for our customers and help them address their challenges. We are a diverse, close-knit community of professionals, where everyone has a voice and opportunity to learn and grow through mutual trust and respect. With a 95 year plus history, we have a track record for success, which includes reported sales of $2.14B in 2020. We serve by the side of our community. Giving back is in our DNA—our team members across more than 50 sites globally are involved with hundreds of charities that have special meaning to them through our West Without Borders team member-led giving program.

 

Summary: Report to the Director, Medical Device R&D, the Research and Development (R&D) Program Manager has responsibility for supporting the delivery and execution of West’s Research and Development Programs. Areas of responsibility of this role will include working with global functions to ensure the execution of research and development large scale and impacting programs remain on track financially, scope is managed, and quality is delivered. This role will be responsible for identifying and managing cross-project dependencies, critical items, risks, and issues. They will communicate at all levels of the organization and be responsible for recognizing and engaging key stakeholders quickly and early in the process.  

                         

Requirements:

  • Education: Requires bachelor’s degree in Engineering field, or equivalent.
  • Experience: 8-10 years’ experience.
  • Track record of successfully managing large-scale, high-risk programs with teams spread across multiple locations.
  • Knowledge of GxP requirements and demonstrated experience managing projects or programs in the medical device and pharma manufacturing industries, knowledge of applicable federal and international regulations.
  • Knowledge of “Agile” methodology process
  • Demonstrated ability to manage multiple globally dispersed individuals and disciplines. Must possess the ability to influence others without direct authority.
  • Experience and capability at delivering written and verbal reports to senior and executive management (CEO, CFO, CIO, other functional SVPs and their direct reports). 
  • Solves complex problems with broad business impact.
  • Works independently, with guidance only in complex situations.
  • Has ability to influence senior leadership, including anticipation of potential objections to adopt a different point of view.


Essential Duties and Responsibilities:

  • Requires specialised depth and breadth of expertise in industry, Program Management, and business acumen.
  • Solves complex problems with broad business impact.
  • Works independently, with guidance only in complex situations.
  • Compliments team deficiencies and drives financial accountability.
  • Interprets internal/external business challenges and recommends best practices to improve products, processes, or services.
  • Drives/Support functions with the preparation of business cases, plans, budgets and artifacts necessary to comply with the Portfolio Management Process, along with supporting the overall program objectives.
  • Cultivates teamwork through leadership and fills knowledge or skills gaps on project teams where needed.
  • Build and maintain strong relationships with customers, business partners, resource managers, and other senior level executives.
  • Communicates complex concepts; anticipates potential objections and influences others to adopt a different point of view
  • Impacts the achievement of customer, operational, project or service objectives; work is guided by department objectives.
  • Has ability to influence senior leadership, including anticipation of potential objections to adopt a different point of view.

 

Project Work:

  • Works with global functions to ensure the execution of research and development large scale and impacting programs remain on track financially, scope is managed, and quality is delivered.
  • Leads programs with high resource requirements, risk, and/or complexity.
  • Identifies and manages cross-project dependencies, critical items, risks, and issues.
  • Leads customer and external support services, e.g. suppliers and contract vendors, to facilitate the development and execution of assigned projects/programs. 
  • Drives transparency of program workloads, financial, commitments, and expectations.
  • Maintain the program related data within the West Project Management System.
  • Monitor resource needs and issues, work closely with resource managers to develop action plans to ensure program commitments remain on track.
  • Manage cross-project and program dependencies.
  • Analyze, Forecast and Report the program budget.
  • Responsible for adherence to the Project & Portfolio Management and New Product Development processes globally and actively work with the project sponsors and their stakeholders to successfully ensure a consistent delivery for all projects globally.
  • Lead/support the development of business cases on assigned programs and track ROI for business initiatives including cost, benefits, and risk.
  • Ensure R&D programs are planned properly, including financials, resourcing, scheduling, and the business case, in support of quality deliverables.
  • Define, drive and manage change management and communications activities that support assigned programs.

 

Other:

  • Performs other duties as assigned based on business needs.
  • Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
  • Exhibits regular, reliable, punctual and predictable attendance.
  • Should be PMP certified.
  • Preferred experience should be in leading commercialization of Medical Devices in compliance with FDA 21 CFR part 820, 93/42/EEC Medical Device Directive (MDD), ISO 13485:2016 Medical Devices, ISO 14971:2019, MDR 2017/745 regulations.
  • Ability to prepare and deliver reports to Sr. Management & Executives.
  • Highly Proficient in Microsoft Applications, including Dev Ops, Agile Methodology, MS Office applications, and Microsoft Project

 

 

 

 

 

 

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status.  If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com.  Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre-employment drug screening.

Apply now »