Manager, Product Engineering

With a passion for life Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers. Are you looking for an inspiring career? You just found it. Job Overview This position delivers engineering solutions to sustain production of implantable medical devices. Responsibilities include managing a team of engineers who work cross-functionally to support design and supplier changes, CAPAs, NCRs, Product Complaints, and other compliance projects. This job requires knowledge of medical device regulations including design controls. Job Responsibilities and Essential Duties Leads design change projects to improve product performance, reduce cost and enhance the manufacturability of commercially released medical devices. Leads CAPAs, NCRs and Product Complaints by investigating and addressing potential product design issues as appropriate. Works with current suppliers on changes to existing purchased components and with new prospective suppliers. Leads Design Reviews at appropriate stages to evaluate adequacy of design requirements, assess the capability of the design to meet requirements and identify and resolve problems. Works cross-functionally on design changes, process improvement projects and quality/compliance initiatives. Creates and executes protocols for Design Verification and Validation activities, engineering studies and feasibility studies. Aids in the selection, design and evaluation of process and test equipment. Creates and executes protocols and reports for process validation, test method validation, equipment qualification and gage R&R studies. Processes change orders to create or revise design input and output documentation. Performs product testing and engineering studies to support design change and investigational activities. Performs Out of Specification (OOS) investigation reports for test failures. Supports Out of Tolerance (OOT) investigations for equipment calibration failures. Supports the development and revision of part specifications and other design documentation. Maintains the Design History File (DHF) and Device Master Record (DMR) throughout the lifecycle of the product based on changes to the product design or manufacturing process. Successfully leads project teams by identifying and mitigating project risks and tracking all project deliverables to completion. Provides technical expertise throughout the supplier selection and evaluation process. Mentors and trains staff on best industry practices and internal company policies and procedures. Provides updates to cross-functional management, including the Senior Leadership Team (SLT) as needed. Serves as the Subject Matter Expert (SME) in internal and external audits. Contributes to the team effort by accomplishing related tasks as needed. Minimum Requirements Bachelor's degree in Engineering or scientific discipline, such as chemical, biomedical, materials, or mechanical engineering. A minimum of seven years' experience in the medical device industry (or other regulated industry) with relevant experience in design controls, production, and process controls and/or R D or related areas. A minimum of three years' experience managing others. Experience leading cross-functional project teams and being a decision-maker. Knowledge of 21 CFR Part 820 and standards relevant to medical devices. Strong experience with Microsoft Office applications (Word/Excel/PowerPoint) is required. Required Knowledge, Skills and Abilities Demonstrated ability to solve technical challenges with cross-functional teams. Strong analytical and problem-solving skills. Strong communication and collaboration skills. Self-motivated with the ability to accomplish project goals with minimal supervision. Ability to empower, motivate and mentor others. Experience with Agile PLM and Minitab desired. Knowledge of Good Documentation Practices (GDP) required. Excellent verbal and written communication skills.

Supervision/Management Of Others:

This position has multiple direct reports. Internal and External Contacts/Relationships Main contacts, internal: Manufacturing Engineering Marketing Materials Management Medical Affairs Operations Program Management Quality Engineering (Design Quality, Operations Quality & Supplier Quality) Regulatory Affairs Research & Development (New Product Development & Product Engineering) Other departments as needed Main contacts, external: Key Opinion Leaders/ SMEs Regulatory authorities, notified bodies and third-party auditors Suppliers Consultants and service providers Others as needed Environmental/Safety/Physical Work Conditions Ensures environmental consciousness and safe practices are exhibited in decisions. May work extended hours during peak business cycles. This position may require some travel to Getinge or partner sites (