Attiva gli avvisi di lavoro via e-mail!

Global Regulatory Affairs Strategy Manager

ZEISS Group

Castiglione Olona

In loco

EUR 30.000 - 50.000

Tempo pieno

Oggi
Candidati tra i primi

Descrizione del lavoro

A leading global technology company is seeking a Global Regulatory Affairs Strategy Manager to drive regulatory strategies in new business initiatives in vision care. Ideal candidates should possess over 7 years of experience in Regulatory Affairs and strong understanding of international frameworks. The role offers opportunities for growth and a supportive culture in Castiglione Olona, Italy.

Servizi

Opportunities for professional growth
Access to cutting-edge technology
Comprehensive training programs
Supportive work culture

Competenze

  • 7+ years of experience in Regulatory Affairs within the life sciences or medical industry.
  • Proven success managing portfolios across multiple projects and geographies.
  • Experience working with global regulatory bodies.

Mansioni

  • Lead and implement global regulatory strategies for new business initiatives.
  • Coordinate with global teams and ensure compliance across markets.
  • Engage with regulatory authorities to influence requirements.

Conoscenze

Strong understanding of international regulatory frameworks
Effective communication skills
Stakeholder engagement
Negotiation skills
Analytical and problem-solving abilities

Formazione

Bachelor's or Master's degree in Regulatory Affairs or related field
Descrizione del lavoro
Overview

Job title: Global Regulatory Affairs Strategy Manager - New Business

Location: Castiglione Olona, Province of Varese, Italy

Contract: Full Time

Salary: [To be defined based on experience]

ZEISS is technology and innovation. Founded in Germany in 1846, we’re an internationally leading technology enterprise operating in the optics and optoelectronics industries, generating more than €10.8 billion in revenue with around 46,000 employees across 50 countries. As a company wholly owned by a foundation, ZEISS is rooted in and committed to responsibility in all its activities. We invest approximately 15% of revenue in science and R&D. As the pioneer of scientific optics, we continue to challenge the limits of human imagination. We’re looking for a Global Regulatory Affairs Strategy Manager - New Business to join us in Castiglione Olona.

Your Role

As a Global Regulatory Affairs Strategy Manager, you will:

  • Lead and implement global regulatory strategies that align with new business initiatives in the vision care sector.
  • Coordinate with global cross-functional teams and external stakeholders to ensure compliance across markets.
  • Anticipate and adapt to evolving regulatory landscapes to support strategic business goals.
  • Develop proactive approaches to regulatory submissions, authorizations, and lifecycle management.
  • Engage directly with regulatory authorities to clarify and influence regulatory requirements.
  • Guide internal teams (e.g., R&D, Clinical, Quality, Marketing) with strategic regulatory input.
  • Support M&A due diligence processes through regulatory assessments.
  • Deliver internal training on regulatory trends and process optimization.
Your Experience

As a Global Regulatory Affairs Strategy Manager, you will have:

  • A Bachelor’s or Master’s degree in Regulatory Affairs, Life Sciences, Medical Industry, Law, IT, or related disciplines.
  • 7+ years of experience in Regulatory Affairs within the life sciences or medical industry.
  • Strong understanding of international regulatory frameworks (e.g. FDA, MDR, ISO 13485, MDSAP).
  • Proven success managing portfolios across multiple projects and geographies.
  • Effective communication, stakeholder engagement, and negotiation skills.
You will ideally have
  • Experience in developing innovative regulatory strategies that create competitive advantage.
  • Strategic thinking with strong analytical and problem-solving abilities.
  • Demonstrated resilience and drive to achieve complex goals.
  • Experience working with global regulatory bodies (e.g., FDA, EMA, PMDA, NMPA, Notified Bodies).
  • Proficiency in English; additional languages are a plus.
Benefits and Culture
  • Opportunities for professional growth and international collaboration
  • Access to cutting-edge technology and world-class facilities
  • Supportive and inclusive work culture
  • Comprehensive training and development programs
Diversity

Diversity is a part of ZEISS. We look forward to receiving your application regardless of gender, nationality, ethnic and social origin, religion, ideology, disability, age, or sexual orientation and identity.

Seniority level
  • Associate
Employment type
  • Full-time
Job function
  • Strategy/Planning and Product Management
Industries
  • Medical Equipment Manufacturing

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

Ottieni la revisione del curriculum gratis e riservata.
oppure trascina qui un file PDF, DOC, DOCX, ODT o PAGES di non oltre 5 MB.