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The Life Science Career Network

CTC are specialised industry experts who can help companies source the best talent and provide reliable HR and consulting services, support varied candidates in finding promising career opportunities and offer the latest in skill development training programmes.

Life Cycle Manager( Regulatory Affairs)

Our client is a leading global player in the Pharmaceutical industry with global headquarters in Basel, Switzerland. They are undergoing a transformation with respect to culture and outside perception. The organisation focusses on novel therapies in Oncology and Ophthalmology and is also currently developing a world-leading pipeline in Neuroscience and Dermatology with one of the strongest pipelines of Phase II/III studies in the world.

We are currently looking for a Life Cycle Manager for our client.

Main Responsibilities:

  • Leads the regulatory lifecycle management and portfolio expansion function (total headcount approx. 180 across, 5 global locations)
  • Directs the function to efficiently implement post approval variations to implement manufacturing changes, process improvement and compliance initiatives
  • Directs the function to provide timely risk assessment and dossier provision for geographic and portfolio expansion of established products worldwide
  • Drives operational excellence and transformation initiatives to optimise department performance
  • Represents Sandoz in appropriate industry forums, engages in external lobbying activities and maintains effective relationships with key regulatory agencies worldwide.
  • As a key member of the Global Regulatory Affairs leadership team actively contribute to the overall strategic direction of the GRA function

Qualifications and Experience:

  • Relevant working/residency permit or Swiss/EU-Citizenship required;
  • Minimum: Degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biology) or equivalent.
  • Desirable: Advanced Degree in Science. Preferable Master.
  • Experienced global regulatory leader with at least 15 years regulatory experience in roles of increasing accountability, ideally in the generic field. Experience from other pharma areas is a plus.
  • Fluent English required (oral and written); German is a plus

Would you like to learn more about CTC and the opportunity outlined? Please, get in contact with us: you may either use the ’apply now’ button, or write an email to us, or reach out to us on the phone.

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Data limite: 04-05-2024

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