{"id":2038464,"url":"https://alion.io/job/getinge-sr-manager-oem-process-engineering","title":"Sr. Manager, OEM Process Engineering","company":{"id":719311,"name":"Getinge","domain":"getinge.com","url":"https://alion.io/company/getinge-2","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"SuccessFactors","truth_index":{"grade":"A","score":100,"open_postings":3,"ghost_share":0,"stale_share":0,"repost_share":0,"time_to_fill_p50_days":23,"computed_at":"2026-10-07T05:47:15Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"senior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Merrimack, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":83000,"max_usd":159000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":4338},"experience_years_min":7,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Microsoft Office","optional":false},{"name":"Supervision","optional":false}],"status":"live","first_seen_at":"2026-10-07T17:01:46Z","employer_posted_date":"2026-10-07","last_verified_at":"2026-10-07T20:37:13Z","board_verified":true,"closed_at":null,"days_open":0,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":0},"description":"With a passion for life\nJoin 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.\nAre you looking for an inspiring career? You just found it.\n\nJob Overview\nManages team of Process Engineers to manufacture medical device finished goods and components for customers. Leads the cross functional team to develop the processes, procure equipment, and set up production lines to deliver product according to customer specifications.\nThis work includes generation of protocols, hands on work with equipment, and working with manufacturing operations to align build schedules. In addition, the incumbent must be able to think through issues and troubleshoot problems related to medical device manufacturing, work with investigations teams to provide robust root causes, technical justifications, understanding changes to equipment and processes, and interact with quality and regulatory departments to help guide decision making. The incumbent will be expected to develop overall validation strategies for specific projects.\nAt a minimum, the person should be able to execute work independently, work with various groups across the organization, be a self-starter, and be able to oversee and lead projects and personnel. The managers goals are to ensure that all projects which support products that are manufactured on behalf of other legal manufacturers are running as intended, that processes are appropriately validated, that processes transferred to operations are robust, and that the team is always looking for areas of improvement.\nJob Responsibilities and Essential Duties\nDevelop, manage, and support a team of technically skilled engineers and technicians who share the job duties and responsibilities noted below.\nProcess verification and validation activities related to the manufacture of medical device products as well as updates/optimizations to existing commercial products.\nDefining Process Verification and Validation strategies for process improvements, changes, and new process development efforts.\nFacilitate all new manufacturing on behalf of customers which are legal manufacturers.\nAchieve manufacturing objectives as specified by the management team by promoting investigation, inventiveness, creativity and solutions to various process, implementation, and material flow/control problems.\nGenerating and executing protocols and writing final reports.\nProject management of overall and individual projects and activities.\nWork to implement a culture of Right-First Time and continuous improvement relative to process procedures and systems. \nPerform and guide nonconformance root cause investigations, gap analyses, process risk assessments, assessment of change controls for process impact.\nProvide expertise to Manufacturing Operations, QA, QC, etc. for trouble-shooting and resolution of process issues as needed. \nAbility to execute and manage multiple projects and activities of extreme complexity simultaneously.\nThe position requires good communication skills to keep customers, peers, direct reports, area management, and site leadership up-to-date with progress of all projects in order to ensure projects are completed in a timely manner and on schedule.\nBe able to work well and interact with cross functional teams that include personnel from Manufacturing Operations, Planning, Quality Engineering, Quality Control, Operations, Regulatory Affairs and Customers.\nMaintain compliance with all regulatory standards for product and personnel safety. \nGeneration of supporting documents for Quality and Regulatory audits and submission as required. \nSupport regulatory inspections through the preparation, defense and interaction with auditors. \nEnsures through monitoring of individual assignments that cross-training is on-going. Develops the leadership of the unit through mentoring, formal and informal training programs. \nCommunicate new ideas, technology advances, and opportunities to management team for review, evaluation and action.\nAssist in identifying the yearly department's needs and helping support it through the budgeting process.\nCreate and maintain a safe environment. Ensure legal requirements and safety policies are enforced.\nAssists in special projects as needed.\nContributes to team effort by accomplishing related duties as requested.\nMinimum Requirements\nBachelor's Degree in Engineering, Industrial Management, or related field, or equivalent.\nMinimum seven years of demonstrated leadership experience within a medical device manufacturing or process development environment.\nMinimum of two years of demonstrated direct management of other engineers, technicians, and/or other technical personnel. \nRequired Knowledge, Skills and Abilities\nAbility to work with flexible and changing production schedules.\nSelf-motivated and have the ability to manage projects, personnel, and problem solve on a regular basis.\nHighly organized with strong project management and technical abilities.\nDemonstrated ability to develop strategies that will help build a positive process engineering and manufacturing operations environment.\nStrong computer skills, including MS Office applications (Word/Excel) are required. \nSupervision/Management OfOthers:\nSupervises Engineers and Technicians. \nInternal and External Contacts/Relationships\nInteracts with internal cross functional teams that include personnel from Manufacturing Operations, Planning, Quality Engineering, Quality Control, Operations, Product Development, and Regulatory Affairs.\nInteracts with external suppliers, vendors, equipment manufacturers, customers etc. \nEnvironmental/Safety/Physical Work Conditions\nEnsures environmental consciousness and safe practices are exhibited in decisions.\nUse of computer and telephone equipment and other related office accessories/devices to complete assignments.\nOffice and clean room production environment\nMay work extended hours during peak business cycles.\n\nAbout us\nWith a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.\nBenefits at Getinge:\nAt Getinge, we offer a comprehensive benefits package, which includes:\nHealth, Dental, and Vision insurance benefits\n401k plan with company match\nPaid Time Off\nWellness initiative & Health Assistance Resources\nLife Insurance\nShort and Long Term Disability Benefits\nHealth and Dependent Care Flexible Spending Accounts\nCommuter Benefits\nParental and Caregiver Leave\nTuition Reimbursement\nGetinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. 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