Senior Science Intelligence & Policy Manager (m/f/d)

CHEPLAPHARM

Berlin

Vor Ort

EUR 90.000 - 130.000

Teilzeit

Vor 2 Tagen
Sei unter den ersten Bewerbenden

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Benefits dieser Stelle

Flexible working models
Company pension provision
Discount platform access
Training & development opportunities

Zusammenfassung

CHEPLAPHARM is a globally active specialty pharmaceutical company seeking a senior professional to lead regulatory affairs initiatives in a dynamic, international environment. The role focuses on collecting and translating regulatory guidelines, ensuring alignment across RA, QA, and PV, and driving digitalization of regulatory processes.

The ideal candidate brings 7+ years' experience, strong leadership, and a proven ability to manage complex, cross-functional topics in line with industry best

Qualifikationen

  • Bachelor’s degree in the natural sciences, pharmacy or medicine; Master’s degree preferred.
  • At least 7 years of relevant professional experience.
  • Leadership experience in matrix or direct environments with strong stakeholder management.
  • Solid understanding of regulatory frameworks, guidelines, and industry best practices.
  • Strong analytical, communication, and coordination skills for cross-functional topics.

Aufgaben

  • Collect, evaluate, and disseminate regulatory guidelines and scientific intelligence across RA, QA, and PV
  • Monitor and analyze developments in pharmaceutical regulations, standards, and competitive trends
  • Build and maintain a centralized Knowledge Hub for up-to-date scientific and regulatory information
  • Drive initiatives to enhance knowledge sharing, digitalization, documentation quality, and cross-functional alignment
  • Support data-driven decision-making by implementing tools and processes that improve transparency and efficiency

Kenntnisse

Regulatory knowledge
Stakeholder management
Leadership
Analytical thinking
Cross-functional coordination
Communication

Ausbildung

Bachelor’s degree in natural sciences/pharmacy/medicine
Master’s degree preferred

Jobbeschreibung

We are an owner-managed, globally active company in the specialty pharmaceuticals sector with a clear mission: to be THE sustainable platform for long-established and trusted pharmaceutical brand products in various therapeutic areas. As a reliable partner to the research-based pharmaceutical industry, CHEPLAPHARM ensures the availability and supply of these medicines for the global market.

This benefits not only our partners, but also patients around the world. We are proud that our specialised business model has enabled us to become one of the world's leading companies in the acquisition of original preparations within 20 years, and we continue to grow. The aspiration of our approximately 800 employees: Together, we want to ‘ACHIEVE MORE’.

What Makes Your Day With Us Special
  • Collect, evaluate, and disseminate regulatory guidelines and scientific intelligence across RA, QA, and PV
  • Monitor and analyze developments in pharmaceutical regulations, standards, and competitive trends
  • Build and maintain a centralized Knowledge Hub to ensure access to up-to-date scientific and regulatory information
  • Drive initiatives to enhance knowledge sharing, digitalization, documentation quality, and cross-functional alignment
  • Support data-driven decision-making by implementing tools and processes that improve transparency and efficiency
What Sets You Apart
  • A Bachelor’s degree in a relevant field, i.e. generally in the natural sciences, pharmacy or medicine, preferably with a Master’s degree
  • At least 7 years of relevant professional experience.
  • Leadership experience in matrix or direct environments with strong stakeholder management skills
  • Solid understanding of regulatory frameworks, guidelines, and industry best practices
  • Strong analytical, communication, and coordination skills with the ability to manage complex, cross-functional topics
What We Offer You Besides The Job
Corporate culture & internationality

A growing company with a diverse, open working environment and employees from around 40 countries.

Flexible working models & work-life balance

Individually customisable working models, including the option to work from another EU country for up to two months per year. Working time account with compensatory time off and 30 days of holiday.

Individual Benefits & Pension Provision

Flexible benefits budget, e.g. for increased company pension provision, fitness and health offers or subsidies for travel and meal costs.

Discounts & Additional Benefits

Access to the corporate benefits platform with discounts at hundreds of partner companies.

Further development & team culture

Internal and external training courses tailored to personal goals, as well as company and team events to strengthen cohesion and celebrate successes together.

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