Project Manager - Engineering

•   Location: Cork
• Req Number: 569972 
• Contract Type: Defined Term

At Boston Scientific, we draw the strength from the unique talents and abilities inherent in a diverse workforce and we believe that the best and most innovative products come from an inclusive workplace where varied viewpoints are welcomed and encouraged. If you require accommodation during the recruitment process please do not hesitate to contact a member of the Talent Acquisition team for a confidential discussion.

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.

Purpose Statement:

This position has the primary function of providing Quality and Compliance expertise and  project management leadership for the implementation of the requirements of EUMDR for site products. This person will act as a Program Manager for MDR & Engineering integration.

Key Roles & Responsibilities:

• Provide leadership, standardization and implementation of best practice for project management within the EUMDR site team
• Provide Quality and Compliance expertise and facilitate Project planning, to support implementation activity
• Ensure regulatory compliance to GMP’s of all medical device regulatory agencies (e.g., FDA, ISO, and MDD).
• Liaise with product support teams, R&D and regulatory on component quality issues and supplier initiatives.
• Liaise with quality, engineering, R&D, Labelling and regulatory accountable persons both internal to the plant and externally within the corporation.
• Lead resolution of problems that impede project progress.
• Responsible for other projects as assigned by the company.
• Deliver project status updates to senior management and project sponsors incorporating status reports and project plan updates.

Education & Experience:

• BSC Science or Engineering degree with 5 or more years within a highly regulated medical device or pharmaceutical environment with proven project management skills (or Equivalent)
• Must have experience with specifically leading multiple projects across highly regulated environment.
• Experience in an MDD, FDA, ISO, GMP regulated environment.
• Strong team member with the ability to identify and drive regulatory compliance improvements.
• Good administrative/organizational ability with excellent attention to detail.
• Excellent communication skills.
• Excellent analytical & decision-making skills

About us

Purpose and Passion – Comprehensive Benefits – Life-Work Integration – Career Growth

At Boston Scientific, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level. With determination, imagination and a deep caring for human life, we’re solving some of the most important healthcare industry challenges. Together, we’re one global team committed to making a difference in people lives around the world. This is a place where you can find a career with meaningful purpose – improving lives through your life’s work.

As a global medical technology leader for more than 35 years, our mission at Boston Scientific (NYSE: BSX) is to transform lives through innovative medical solutions that improve the health of patients. If you’re looking to truly make a difference to people both around the world and around the corner, there’s no better place to make it happen.

Boston Scientific is an Equal Opportunity Employer – Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Disability, Veteran