ITM is a privately owned biotechnology and radio­pharma­ceutical group of companies dedicated to the development, production and global supply of targeted diagnostic and therapeutic radio­pharma­ceuticals and radio­isotopes for use in cancer treatment. We are developing a proprietary portfolio and growing pipeline of targeted treatments in various stages of clinical development addressing cancers such as neuro­endocrine cancers or bone metastases. Our main objectives are to significantly improve treatment outcomes and quality of life for cancer patients through a new generation of Targeted Radio­nuclide Therapies in Precision Oncology. The head­quarters are located in the heart of the research center of the Technical University of Munich (TUM).

We would like to fill the following permanent vacancy in a remote-based or hybrid working model in Garching as soon as possible.

Deputy Graduated Plan Officer (GPO) / Stellvertretender Stufenplanbeauftragter (f/m/d)

• Fulfil the role of the GPO during the absence of the appointed GPO, according to the relevant legislation and guidelines
• Set up and manage a pharmacovigilance system (§ 63a of AMG)
• Collect and evaluate reports of drug risks and coordinate the necessary measures and responsibility for fulfilling notification obli­ga­tions insofar as they relate to drug risks (§ 63a of AMG and § 19 of AMWHV)
• Inform the qualified person of the necessary measures (§ 19 of AMWHV & § 14 of the Medicines Act)
• Inform the competent authority immediately of any defect that could lead to a recall or an unusual restriction on distribution and shall also state the countries to which the medicinal product was shipped or exported
• Inform the authority immediately of any suspicion of counterfeit medicinal products or active ingredients; in the case of medicinal products intended for human use, the marketing authorisation holder shall also be informed

• Completed degree of a Medical Doctor, Pharmacist or equivalent with extensive work experience in a similar role in pharma­covigilance
• Experience working in a cross-functional team within a matrix environment
• Advanced knowledge of regulations gov­ern­ing Pharma­covigilance in the pharma­ceutical industry and R&D processes in Europe and globally
• Excellent analytical, problem-solving, strategic planning, and inter­personal skills
• Open to changes, suggestions and inno­va­tions; drive for continuous improvement
• Fluent in English and German

• Exciting challenges in an up-and-coming and fast-growing company with a high degree of creative freedom
• An open working atmosphere in an international corporate culture with short communication channels
• Comprehensive onboarding programme
• Flexible working hours with home office options
• Attractive special payments
• Just a good salary? Not with us! We also offer you:
  • Employee participation programme
  • Job bike or subsidised job ticket
  • Above-average contribution to the company pension scheme
  • Individually tailored further training programme (including German and English courses)
  • Health promotion programmes (e.g. EGYM Wellpass, subsidy for local fitness studio, sponsorship of sporting events, various lifestyle coaching sessions)