Expires soon Nestlé

Medical Advisor (m/w) - (80-100%)

  • Zürich (Bezirk Zürich)
  • Legal

Job description

Nestlé Skin Health is a global leader in improving the quality of life by delivering innovative medical solutions for the health of skin, hair and nails throughout people's lives. Nestle Skin Health aims to meet the needs of healthcare professionals and consumers through constant innovation in technology and products to protect and improve the health of the skin and treat skin diseases.
Nestlé Skin Health is a subsidiary of Nestlé.
For our office in Zurich- Switzerland we are currently looking for a

Medical Advisor (m/w)
(80-100%)

In this challenging and dynamic role, you will report to the Head of Medical and Regulatory Affairs. You will provide medical expertise for prescription drugs, self-medication and cosmetics to ensure high quality scientific and medical advice, education and information is provided on the local market. You will work closely with the commercial and medical departments, as well as customer service.
Leading, developing, maintaining and improving the medical information system and documents is also part of your role as well as acting as a back-up for the Field Based Medical Affairs Manager.

Accountabilities:
Medical Affairs:
· Provides medical expertise under the leadership of the Head of Medical & Regulatory Affairs in business areas to ensure high quality scientific and medical advice, education and information is provided on the local market
· Works closely with the commercial and medical departments.
· Active participation in the Brand Team Meetings and annual brand planning for Acne, Rosacea and Emolliences and coordination of external projects in those areas with the Field Based Medical Affairs Manager in alignment with the Head of Medical Affairs
· Develops the medical affairs plan for Acne, Rosacea and Emolliences according local and global strategy
· Participates at Medical Team Meetings and provides information on medical information KPIs, status and progress of Investigator initiated trials as well as on project needs/progress/impact
· Monitors the advertising material of competitors
· Medical/Scientific evaluation of advertising materials according to the SOP
· Manage internal approval and submission process or requests for investigator initiated trials to support independent clinical/ preclinical research with global Medical Affairs
Medical Information:
· Leads, develops, maintains and improves the medical information system
· Develops and maintains medical information documents i.e. standard responses, medical FAQs in cooperation with local and global experts
· Answers and documents medical information questions according to the SOP
Medical Training :
· Leads, develops, maintains current files on product-relevant medical literature and provides scientific/medical training for internal staff in all business areas in cooperation with the Field Based Medical Affairs Manager if necessary.
· Supports the introduction of new products, new areas of application or repositioning, trains the sales force on important messages for study interpretation and objection handling

Compliance:
· Follows local regulations an laws such as HMG, AWV, Pharmacodex, SWISS MEDTECH CODE, LGM, LGV and VKos
· Responsible for developing and implementing the necessary medical affairs SOPs at local level to meet company and country regulations under supervision of the head of medical affairs
· Comply with all corporate legal policies, procedures and business ethics standards
· Develops succinct statements for all pharmaceutical products
Pharmacovigilance:
· Triage of reported adverse events from medical information for all products in the prescription, self-medication and aesthetic correction (fillers and cosmetics) areas
· Supports pharmacovigilance, close cooperation with the local safety officer

Your Profil:
· University degree (MD, PharmD, PhD, pharmacist)
· 3+ years experience in the pharmaceutical industry ideally in medical affairs with therapeutically experience in dermatology
· Experience in interpreting findings from medical meetings, clinical studies and medical publications
· Good compliance knowledge of Swiss pharmaceutical regulatory and ethical guidelines required (e.g. Federal Act on Medicinal Products and Medical Devices; Pharmacodex etc.)
· English, German fluency as well as very good French skills
· Committed team player

Looking forward to your application.
More details on behavioral, functional and technical competencies will be provided upon application.

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