Manager, Integration, Depl. Sys. & Dev

Biopharma Careers; Zuchwil; Vor Ort; CHF 120.000 - 160.000; Vollzeit

Zusammenfassung

Johnson & Johnson is seeking a Manager, Integration, Depl. Sys. & Dev in Regulatory – Other.

Based across multiple countries, including Switzerland, the role focuses on leading regulatory system integration and deployment, partnering with regulatory, quality, IT, and business teams to ensure compliant implementations. The position requires strong project management and stakeholder management skills, with 6–8 years of experience in regulatory systems and a global, matrixed environment.

Qualifikationen

• Bachelor’s degree in Regulatory Affairs, Information Systems, Engineering, Life Sciences, or related discipline (required).
• Advanced degree or RAC or related certifications preferred.

Aufgaben

• Lead and manage regulatory system integration, deployment, and development initiatives.
• Partner with Regulatory Affairs, Quality, IT, and business teams to define system requirements.
• Support deployment and ongoing enhancement of regulatory systems and tools.
• Oversee change management related to regulatory system updates and integrations.
• Ensure regulatory processes align with internal policies, quality systems, and regulations.
• Support audits, inspections, and assessments related to regulatory systems and data.
• Monitor regulatory and system changes and assess impact on tools and processes.
• Drive continuous improvement for system efficiency, scalability, and compliance.

Kenntnisse

Regulatory systems

IT systems integration

Stakeholder management

Project management

Regulatory compliance

Analytical thinking

Ausbildung

Bachelors in Regulatory Affairs

Advanced degree or RAC

Tools

RIM systems

Regulatory information systems

Jobbeschreibung

At 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 .

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

Regulatory Affairs Group

Job Sub Function

Regulatory Affairs

Job Category

Professional

All Job Posting Locations

Zuchwil, Switzerland

Job Description

DePuy Synthes is recruiting for a(n) Manager, Integration,Depl. Sys. & Dev, Regulatory – Other,locatedinRaynham, Massachusetts, West Chester, PA, Warsaw, IN, Palm Beach Gardens, FL, NJ or Zuchwil Switzerland

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

Raynham, Massachusetts: Requisition Number: R-074954

Zuchwil, Switzerland - Requisition Number: R-097573

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Johnson & 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. Should 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.

Key Responsibilities

• Lead and manage regulatory system integration, deployment, and development initiatives in alignment with regulatory and compliance requirements.
• Partner with Regulatory Affairs, Quality, IT, and business teams to define system requirements and ensure compliant implementation.
• Support deployment and ongoing enhancement of regulatory systems and tools, ensuring data integrity and usability.
• Oversee change management activities related to regulatory system updates, integrations, and enhancements.
• Ensure regulatory system processes align with internal policies, quality system requirements, and applicable regulations.
• Support audits, inspections, and assessments related to regulatory systems and data.
• Monitor regulatory and system‑related changes and assess impactstotools, processes, and integrations.
• Drive continuous improvement initiatives to enhance regulatory system efficiency, scalability, and compliance.

Qualifications

Education:

• Bachelor’s degree in Regulatory Affairs, Information Systems, Engineering, Life Sciences, ora relateddiscipline (required).
• Advanced degree or professional certification in Regulatory Affairs, Information Systems, or related fields (preferred).

Experience and Skills:

Required

• Typically6-8 years of progressive experience in regulatory systems, regulatory operations, IT systems integration, or a related role within a regulated industry.
• Experience supporting system integration, deployment, or development initiatives in a compliance‑driven environment.
• Strong understanding of regulatory processes and data requirements.
• Ability to translate regulatory and business requirements into system solutions.

Preferred

• Experience in medical devices, healthcare, or other highly regulated industries.
• Familiarity with regulatory information management (RIM) systems or related platforms.
• Experience supporting audits or inspections involving regulatory systems.
• Experience working in a global or matrixed organization.
• Demonstrated experience driving system or process improvement initiatives.
• Effective written and verbal communication skills.
• Strong project management, problem‑solving, and stakeholder management skills.

Other

• Language: Englishrequired.
• Travel: Limited; occasional domestic or international travel as needed.
• Certifications: Regulatory Affairs Certification (RAC) or relevant systems/project certifications preferred but notrequired.

For more information on how we support the whole health of our employees throughout their wellness,careerand life journey, please visit www.careers.jnj.com .

Johnson & Johnsonisan Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal,stateor local law. We actively seek qualified candidates who areprotectedveterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to requestan accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contactAskGSto be directed to your accommodation resource.

Required Skills

Analytical Reasoning, Business Writing, Coaching, Compliance Risk, Fact-Based Decision Making, Industry Analysis, Legal Support, Process Improvements, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Risk Assessments, Strategic Thinking, Technical Credibility

Preferred Skills

Analytical Reasoning, Business Writing, Coaching, Compliance Risk, Fact-Based Decision Making, Industry Analysis, Legal Support, Process Improvements, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Risk Assessments, Strategic Thinking, Technical Credibility