Ph3Business Process Manager Verification DFM /h3 pFull-time (100%) Associate /p pbAbout SHL Medical /b /p pSHL Medical is a world-leading provider in the design, development, and manufacturing of advanced self-injection devices. With a global team of 6,000 employees, we partner with leading pharmaceutical and biotech companies to deliver innovative autoinjectors, pen injectors, and other drug delivery systems that ensure effective treatment for patients. Headquartered in Switzerland since 2018, with key operations in Sweden, Taiwan, and the US, we are united by a commitment to innovation, impact, and growth. Together, we empower our people to develop solutions that make a meaningful difference in the lives of millions of patients while fostering a supportive, inclusive, and dynamic workplace for our colleagues. /p pbJob Overview /b /p pThe Business Process Manager Verification Design for Manufacturing (DFM) plays a key role in driving process excellence across product development, with a strong focus on Product Verification and DFM practices. This position ensures that processes are designed, implemented and continuously improved to enhance product quality, compliance and manufacturability. /p pAs a strategic enabler within the technical organization, the role supports our mission to manage, develop and optimize end-to-end development processes. Working with teams in RD, Quality, Regulatory, Manufacturing Engineering and Operations, the business Process Manager Verification DFM will ensure that processes within the technical organization support business objectives and operational excellence. Based in Zug, this role will collaborate closely with other process managers and cross‑functional teams to ensure effective and efficient workflows. /p pUltimately, the Business Process Manager Verification DFM ensures that robust, efficient and compliant processes enable faster innovation, seamless collaboration and sustainable product development across SHL. /p pbMain Responsibilities /b /p ul liDesign, implement and continuously improve end‑to‑end business processes related to Design Verification, DFM and associated domains (Design, Risk Management, Testing, Manufacturing Readiness). /li liEnsure compliance with regulatory and quality standards throughout the product lifecycle, including medical device regulations. /li liCollaborate with RD, Quality, Regulatory, Manufacturing Engineering, Operations, and IT to harmonize processes, documentation, and align with production requirements. /li liDevelop and maintain process documentation (Work Instructions, Templates, Guidelines) and training materials ensuring compliance with medical standards and company QMS. /li liConduct workshops, training sessions and stakeholder interviews to identify process gaps, drive adoption and support change management initiatives. /li liTranslate business needs into functional solutions and work with system architects to implement and validate PLM solutions. /li liMonitor process performance, report KPIs, and collect user feedback to drive continuous improvement. /li /ul pbMinimum Qualifications /b /p ul li5+ years of relevant experience and success in process management within the medical device or pharmaceutical industry. /li liStrong knowledge of product development, Verification processes, Design Controls and DFM principles. /li liExcellent strategic thinking, problem‑solving and analytical capabilities with a focus on continuous improvement and innovation. /li liAbility to influence and communicate effectively across all organizational levels, promoting transparency and collaboration. /li liAbility to work in a fast‑paced, global environment with multiple priorities. /li liBachelor’s or Master’s degree in Engineering, Quality Management, Industrial Engineering or related field. /li liFluency in English is required. /li /ul pbPreferred Qualifications /b /p ul liFamiliarity with PLM systems and digital documentation workflows (e.g. Signavio). /li liExperience applying agile methodologies in process design. /li liCertification in Lean Six Sigma, Process Management or Project Management (e.g. PMI, IPMA) is a plus. /li liTraining in DFM methodologies and Verification standards preferred. /li liExperience with ISO 13485, FDA regulations, or similar compliance frameworks. /li liGerman skills are a plus. /li /ul pbWe Offer: /b /p ul liChallenging assignments in a fast‑growing and innovative industry. /li liA multicultural team and modern working environment with state‑of‑the‑art facilities and technologies. /li liA place where we take pride in the inclusive and collaborative environment we have built - one where a true sense of belonging fosters meaningful exchange and shared growth. /li liVarious opportunities for personal and professional development within a global organization. /li liFlexible hours and hybrid working policy. /li /ul pInterested in joining SHL Medical and in supporting us with your expertise and personality? Then we look forward to receiving your application to our Talent Acquisition Department. /p pFor more information on SHL Medical, please visit: shl‑medical.com/careers /p pbPlease note: We do not accept applications from recruitment agencies for this position. /b /p pWe like to keep things simple and efficient. Once you’ve applied, it may take up to three weeks to review your application and get the first call with a recruiter. /p h3Grounded in belonging, we strive for excellence /h3 pWith almost 6,000 employees of 77+ different nationalities, we take pride in the inclusive and collaborative environment we have built - one where a true sense of belonging fosters meaningful exchange and shared growth. Together, we invest in our future to maintain our leadership position in self‑injection solutions. /p /p #J-18808-Ljbffr