Senior Packaging Development Manager

ppAt Johnson Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com. /p pAs guided by Our Credo, Johnson Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson Johnson, we respect the diversity and dignity of our employees and recognize their merit. /p h3Job Function /h3 h3Job Sub Function /h3 h3Job Category /h3 h3All Job Posting Locations /h3 pZuchwil, Switzerland /p h3Job Description /h3 pJohnson Johnson is currently seeking a Sr. Manager, Packaging Development to join our team. The role can be based in the following DePuy Synthes sites: Zuchwil, Switerzland; Cork, Ireland; Raynham, Massachusetts; Raritan, New Jersey; Palm Beach Gardens, FL; Warsaw, Indiana. /p h3At Johnson Johnson /h3 pAt Johnson Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at /p h3About JJ MedTech /h3 pAt Johnson Johnson MedTech, we unleash diverse healthcare expertise, purposeful technology, and a passion for people to transform the future of medical intervention and empower everyone to live their best life possible. For more than a century, we have driven breakthrough scientific innovation to address unmet needs and reimagine health. In surgery, orthopedics, vision, and interventional solutions, we continue to help save lives and create a future where healthcare solutions are smarter, less invasive, and more personalized. /p h3Position Overview /h3 pThe Sr. Manager, Packaging Development is a critical leader and member of the Trauma and Extremities Technical Operations LT who has responsibility to lead their team in the design, development, and commercialization of packaging technologies for the entire product’s lifecycle – from new product introduction through end of life. This leader will be responsible to develop and build a high performing team who will identify and deploy contemporary, industry leading packaging solutions and best practices to the Trauma Extremities business which deliver on product design requirements, ensure quality/compliance, meet or exceed cost targets, and delight our customers. This leader will be a key voice in shaping the Product Strategy and CoGS Roadmaps for the business, whose team will be accountable to delivery on critical project deliverables for both new product introductions and lifecycle management. /p h3Tasks Responsibilities /h3 ul liLead, motivate and develop a team of seasoned packaging engineering professionals and project managers to deliver excellence. /li liOwnership of packaging development packaging design, development, and commercialization from new product launch through end of life. /li liSynthesize and deploy enterprise packaging strategy aligned with key business partners across RD, Commercial, Value Stream, New Product Introductions, Operations, Network Strategy, Regulatory Affairs, Quality, and Product Labeling /li ligEnsure strong technical development of team and partnership with critical functions in the development, testing, validation, and commercialization of device packaging solutions for both new and existing products. /li liLead team in the identification, prioritization, and execution of packaging continuous improvement projects. /li liEnsure packaging validations are completed on time, on budget, and within quality compliance/expectations with third party suppliers, as applicable. /li liEnsure packaging technologies for currently marketed products meet or exceed both internal DePuy Synthes and/or external quality/compliance/environmental standards. /li liMaintain departmental and project budgets and ensure timely capital and expense spend within targets. /li /ul h3Qualifications Experience /h3 ul liA minimum of 8-10 years of experience in packaging, engineering, quality, operations, or related supply chain discipline required. /li liExperience working in the Medical Device or other regulated industry is preferred. /li liExperience in Package Engineering and packaging supplier selecftion/management is preferred. /li liPast direct people management experience is preferred. /li liThe ability to successfully lead and support transformational change across functions involving innovative solutions is required. /li liThe ability to lead and/or support multiple project teams simultaneously is required. /li liExperience with Business Excellence and Project Management methodologies is preferred. /li liKnowledge of sterile packaging material characteristics and validation practices is preferred. /li liPast experience in process development and in writing and executing validations is preferred. /li liKnowledge of ISO13485, ISO11607, ISTA and ASTM standards and their application to medical devices is preferred. /li liUnderstanding of statistical analysis is required. /li liStrong financial acumen, including the ability to complete financial analysis for capital purchases, estimate manufacturing costs, estimate component cost is preferred, and support NPV/IRR calculations for investment decisions is preferred. /li liProficiency in Microsoft Office applications are required /li /ul pJohnson Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. /p pShould you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes. /p pWe will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. /p h3Required Skills /h3 h3Preferred Skills /h3 ul liCompetitive Landscape Analysis /li liCompliance Frameworks /li liCreating Purpose /li liDeveloping Others /li liGood Manufacturing Practices (GMP) /li liInclusive Leadership /li liLeadership /li liLean Supply Chain Management /li liManaging Managers /li liPackage and Labeling Regulations /li liPackage Management /li liProduct Packaging Design /liliRisk Assessments /li liScience /li liTechnology /li liEngineering /li liand Math (STEM) Application /li liStandard Operating Procedure (SOP) /li liSustainability /li liSustainable Packaging /li liTransparency Reporting /li /ul /p #J-18808-Ljbffr