Product Manager Sport & Shoulder

This job is with Johnson & Johnson, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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 .

As 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.

Job Function:

Marketing

Job Sub Function:

Product Management

Job Category:

Professional

All Job Posting Locations:

Zuchwil, Switzerland, Zug, Switzerland

Job Description:

Product Manager Sport & Shoulder

Job Description:

About Orthopedics

Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Are you passionate about improving and expanding the possibilities of Orthopedics? Ready to join a team that's reimagining how we heal? Our Orthopedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

Product Manager Sport & Shoulder for the Swiss Market

For our Swiss Sport and Shoulder Reconstruction business, we are seeking a strong, passionate, customer-focused and communicative personality to join our successful Sports & Shoulder team, starting immediately or by agreement. If you are looking to take the next step into a dynamic, high‑performance environment, this role offers the perfect opportunity. We provide a motivated and committed individual with a diverse set of responsibilities in a modern, forward‑thinking company, where you can make a meaningful impact and grow.

Tasks:

• Responsible for several different product groups as well as product portfolio management over the entire life cycle
• Serves as competent contact person (internally and externally) regarding products as well as for the entire business, with a focus on our arthroscopic and shoulder reconstruction business
• Development of launch plans and product strategies in the field of Sport & Shoulder Reconstruction, monitoring and implementation of the strategy
• Execution of high-quality new product launches as well as monitoring and implementation of the product strategy in the Swiss market
• Support and close collaboration with Swiss based sales representatives
• Responsible for market segmentation, targeting and product positioning in the Swiss market
  
  

6182110 Class III Quality Engineer ![CDATA[ p strong em This job is with Johnson Johnson, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. /em /strong /p pAt Johnson amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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 spanjnj.com/span./ppAs guided by Our Credo, Johnson amp; 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 amp; Johnson, we respect the diversity and dignity of our employees and recognize their merit./ppstrongspanspanJob Function: /span/span/strong/pSupply Chain Engineeringp/pp/ppstrongspanspanJob Sub /span/spanspanspanFunction: /span/span/strong/pQuality Engineeringp/pp/ppstrongJob Category:/strong/pScientific/Technologyp/pp/ppstrongAll Job Posting Locations:/strong/pYokneam, Haifa District, Israelp/pp/ppstrongJob Description:/strong/pdivh3strongPosition Summary/strong/h3pThe strongClass III Quality Engineer/strong is responsible for supporting the development of Class III medical devices in full compliance with Quality Assurance (QA) standards, regulations, and internal Johnson amp; Johnson procedures.br /The role covers product development activities, risk management, DHF ownership, quality process implementation, audits, and cross‑functional collaboration between HTC and the BWI QA organization./ph3/h3h3strongKey Responsibilities/strong/h3h3strongProduct Development Quality (Class III Devices)/strong/h3ulliEnsure product development activities comply with relevant standards, regulations, and internal processes./liliLead and maintain Risk Management activities including xFMEA, risk files, and investigations./liliReview defect meetings, clinical readiness results, and escalate potential regulatory or safety issues./liliLead design control processes and quality deliverables for Class III devices (NPD and engineering builds)./liliSupport and lead quality activities during transfer from Ramp;D to manufacturing./liliAssess and approve design changes./liliMaintain and present Quality Plans, metrics, and project status./liliLead quality investigations and escalate product‑related issues when required./li/ulh3strongTools amp; Test Equipment Quality/strong/h3ulliLead QA activities for development of tools and jigs./liliReview and approve test equipment qualification and documentation./li/ulh3strongDesign History File (DHF) Management/strong/h3ulliOwn DHF management for Class III products./liliDefine and approve QA deliverables for Ramp;D projects./liliConduct credibility checks to ensure documentation accuracy and compliance./liliEnsure HTC development processes align with BWI Quality processes./liliIdentify and implement continuous improvements in new product development processes./li/ulh3strongQA Compliance/strong/h3ulliAct as QA representative for compliance with corporate Jamp;J NPD standards./liliPerform internal product and process audits./liliSupport preparation for external audits./li/ulh3strongGeneral Responsibilities/strong/h3ulliCommunicate business‑related issues or opportunities to management./liliEnsure compliance with all applicable regulations, policies, and procedures./liliPerform additional tasks as assigned./li/ulh3/h3h3strongEducation amp; Experience/strong/h3h3strongRequired / Preferred Education/strong/h3ulliB.Sc. in Engineering (preferred)./liliAdvantage: Quality Assurance certifications (CQE, CSQE, CQM, CRE)./li/ulh3strongExperience/strong/h3ulliAdvantage: Experience in a Quality role, preferably in active medical devices or related industry./liliAdvantage: Experience in statistical data analysis methodologies./li/ulh3strongRequired Knowledge amp; Skills/strong/h3ulliUnderstanding of ISO and regulatory standards (ISO 13485, ISO 14971, MDD/MDR)./liliStrong interpersonal and communication skills./liliAbility to work with remote team leadership./liliStrong English proficiency (spoken and written)./liliHigh integrity, self‑motivation, and ability to work independently or in a team./liliResults‑driven, detail‑oriented, and organized./li/ulp /p/divp/pp/pp /pp /ppstrongRequired Skills: /strong/pp /pp /ppstrongPreferred Skills:/strong/pCustomer Centricity, Data Savvy, Document Management, Execution Focus, Good Automated Manufacturing Practice (GAMP), Issue Escalation, Lean Supply Chain Management, Process Control, Process Improvements, Quality Control (QC), Quality Services, Quality Standards, Quality Systems Documentation, Science, Technology, Engineering, and Math (STEM) Application, Supervision, Supply Planning, Technologically Savvy]] Hospital Health Care Full-time Yokneam, Haifa District Israel IL https://mygwork.com/jobs/johnson-johnson-class-iii-quality-engineer-1?src=linkedinutm_source=linkedinutm_medium=referralutm_campaign=jobs Johnson Johnson

![CDATA[ p strong em This job is with Johnson Johnson, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. /em /strong /p pAt Johnson amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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 spanjnj.com/span./ppAs guided by Our Credo, Johnson amp; 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 amp; Johnson, we respect the diversity and dignity of our employees and recognize their merit./ppstrongspanspanJob Function: /span/span/strong/pSupply Chain Engineeringp/pp/ppstrongspanspanJob Sub /span/spanspanspanFunction: /span/span/strong/pQuality Engineeringp/pp/ppstrongJob Category:/strong/pScientific/Technologyp/pp/ppstrongAll Job Posting Locations:/strong/pYokneam, Haifa District, Israelp/pp/ppstrongJob Description:/strong/pdivh3strongPosition Summary/strong/h3pThe strongClass III Quality Engineer/strong is responsible for supporting the development of Class III medical devices in full compliance with Quality Assurance (QA) standards, regulations, and internal Johnson amp; Johnson procedures.br /The role covers product development activities, risk management, DHF ownership, quality process implementation, audits, and cross‑functional collaboration between HTC and the BWI QA organization./ph3/h3h3strongKey Responsibilities/strong/h3h3strongProduct Development Quality (Class III Devices)/strong/h3ulliEnsure product development activities comply with relevant standards, regulations, and internal processes./liliLead and maintain Risk Management activities including xFMEA, risk files, and investigations./liliReview defect meetings, clinical readiness results, and escalate potential regulatory or safety issues./liliLead design control processes and quality deliverables for Class III devices (NPD and engineering builds)./liliSupport and lead quality activities during transfer from Ramp;D to manufacturing./liliAssess and approve design changes./liliMaintain and present Quality Plans, metrics, and project status./liliLead quality investigations and escalate product‑related issues when required./li/ulh3strongTools amp; Test Equipment Quality/strong/h3ulliLead QA activities for development of tools and jigs./liliReview and approve test equipment qualification and documentation./li/ulh3strongDesign History File (DHF) Management/strong/h3ulliOwn DHF management for Class III products./liliDefine and approve QA deliverables for Ramp;D projects./liliConduct credibility checks to ensure documentation accuracy and compliance./liliEnsure HTC development processes align with BWI Quality processes./liliIdentify and implement continuous improvements in new product development processes./li/ulh3strongQA Compliance/strong/h3ulliAct as QA representative for compliance with corporate Jamp;J NPD standards./liliPerform internal product and process audits./liliSupport preparation for external audits./li/ulh3strongGeneral Responsibilities/strong/h3ulliCommunicate business‑related issues or opportunities to management./liliEnsure compliance with all applicable regulations, policies, and procedures./liliPerform additional tasks as assigned./li/ulh3/h3h3strongEducation amp; Experience/strong/h3h3strongRequired / Preferred Education/strong/h3ulliB.Sc. in Engineering (preferred)./liliAdvantage: Quality Assurance certifications (CQE, CSQE, CQM, CRE)./li/ulh3strongExperience/strong/h3ulliAdvantage: Experience in a Quality role, preferably in active medical devices or related industry./liliAdvantage: Experience in statistical data analysis methodologies./li/ulh3strongRequired Knowledge amp; Skills/strong/h3ulliUnderstanding of ISO and regulatory standards (ISO 13485, ISO 14971, MDD/MDR)./liliStrong interpersonal and communication skills./liliAbility to work with remote team leadership./liliStrong English proficiency (spoken and written)./liliHigh integrity, self‑motivation, and ability to work independently or in a team./liliResults‑driven, detail‑oriented, and organized./li/ulp /p/divp/pp/pp /pp /ppstrongRequired Skills: /strong/pp /pp /ppstrongPreferred Skills:/strong/pCustomer Centricity, Data Savvy, Document Management, Execution Focus, Good Automated Manufacturing Practice (GAMP), Issue Escalation, Lean Supply Chain Management, Process Control, Process Improvements, Quality Control (QC), Quality Services, Quality Standards, Quality Systems Documentation, Science, Technology, Engineering, and Math (STEM) Application, Supervision, Supply Planning, Technologically Savvy]]