Director - New Product Introduction and Lifecycle - Schaffhausen, Schweiz - Johnson & Johnson
Beschreibung
Cilag AG, a member of the Johnson & Johnson Family of Companies since 1959, is recruiting for a Director - New Product Introduction and Lifecycle Management (NPI & LCM)
The Schaffhausen site acts as one of the major producers of the Swiss pharmaceutical industry and one of the most important employers in the Schaffhausen region.
The Director - NPI & LCM is responsible for leading a team ensuring the successful introduction and launch of new products into our aseptic pharmaceutical manufacturing environment.
Their efforts will contribute to J&J's commitment to both operational excellence and the growth and well-being of a diverse workforce.
Key Responsibilities:
- Direct managers and senior individual contributors in a dynamic environment, ensuring that project plans are comprehensively reviewed, implemented, and completed on schedule and within budget.
- Develop and implement a comprehensive strategy for the introduction of new products in close collaboration with Research and Development, Operations, Quality Functions, Value Chain Management, and Manufacturing Scient and Technology (MSAT).
- Collaborate closely with internal and external partners, including suppliers, contract manufacturers, and regulatory authorities, to ensure timely and successful product introductions and lifecycle management.
- Lead all aspects of the entire product lifecycle, from development and introduction to postmarket surveillance and phaseout, ensuring compliance with regulatory requirements and quality standards.
- Find opportunities for process optimization and continuous improvement in product development and introduction processes.
- Create, maintain, and upgrade product technical knowledge and support the overall Value Chain (VC) knowledge infrastructure.
- Support Drug Product process transfers between manufacturing sites (internal or external).
- Serve as Technology Champion within the domain of parenteral production.
- Participate in technical, quality, and compliance risk assessments and develop mitigation strategies and possible BCP options.
- Support inspection readiness and support nonconformance and failure investigations.
- Participate and present at industryrelated conferences and seminars.
Qualifications:
Education:
- Minimum of a Bachelor's/University or equivalent degree in Pharmacy, Chemistry, Biotechnology, or an equivalent scientific field is required; M.S./ PhD preferred
Experience and Skills:
Required:
- Minimum 10 years of relevant work experience
- Experience with New Product Introduction into the pharmaceutical manufacturing environment
- Thorough knowledge of regulatory requirements and quality standards in the pharmaceutical industry
- People management or leadership experience (direct or indirect reports)
- Strong communication skills to effectively motivate and lead interdisciplinary teams and interact at various levels of the organization, including senior management
- Strong creative and analytical thinking skills and a track record of developing innovative solutions for complex challenges
- Demonstrated mentality to recognize opportunities, a willingness to take calculated risks, and the ability to encourage ambitious thinking
Preferred:
- Lean, Six Sigma, or Process Excellence methodologies experience, training, or certification
- Experience supporting inspections or audits
Other:
- Requires proficiency in both English and German (written and spoken); additional language skills are a plus
- May require up to 10% domestic and international travel
- Requires the ability, through our flexible work policy, to work onsite a minimum of three days each week, with the option for two remote workdays each week
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