Senior Consultant Arzneimittel - Pharmacovigilance (m/f/d)

Tentamus Group GmbH is an internationally growing medium-sized company specializing in quality and monitoring services in the fields of food, feed, pharmaceuticals and cosmetics. Our success is based on the expertise of our over 4000 employees at more than 95 locations worldwide. The decentralized structure of our laboratories not only creates flexibility for our customers, but also offers diverse career opportunities in a dynamic, international environment. We place great emphasis on a culture of diversity and inclusion in which all employees are treated equally regardless of origin, gender, sexual orientation, religion or disability. Anti-discrimination and equal opportunities are not just principles for us, but a matter of course. We promote a respectful and open working environment in which everyone can fully develop their potential. Become part of the Tentamus family and shape the future of quality testing with us – in an inclusive and respectful world of work! Our company TentaConsult Pharma & Med GmbH is a dynamic consulting and service company specializing in the fields of medicines, medical devices, dietary supplements and cosmetics. Our field of activity includes services in Regulatory & Clinical, Biological Affairs and Quality Management. We support our customers in the development, admission and market launch of their products and take over responsible roles such as legal manufacturers, EU-REP, PRRC or relevant functions in the ISO 13485 environment. Senior Consultant Pharmacovigilance (m⁠/⁠w⁠/⁠d)

We are looking for experienced scientists:inside or pharmacists:inside (m⁠/⁠w⁠/⁠d) as Senior Consultant Medicine - Pharmacovigilance for the further expansion of our consulting activities for the pharmaceutical industry and the healthcare industry. You support your college in customer projects and guide your own, including: Consultation in GVP-Fragestellung-from QMS-Themen, regular research, case report and signal management to the qualification of PV service providers Communication with customers and authorities Takeover of legal functions, such as QPPV, Step Plan Officer Person or PV Officer Support of customers through cooperation in and care of their and our own PV systems

We are looking for pragmatic “Macherinnen” (m⁠/⁠w⁠/⁠d), who feel comfortable in smaller and medium sized companies: You have a degree or comparable training, ideally with a scientific orientation (e.g. biology, chemistry, LM chemistry, pharmacy) or engineering sciences, as well as the qualification and expertise as a grading officer Person and EU QPPV Sometimes, depending on the project, e.g. for government inspections or service provider audits, willingness to travel to clients. You can gain experience in consulting and services and already have specific experience in regulatory matters and pharmacovigilance for medicinal products. You have experience in developing and maintaining pharmacovigilance systems for medicinal products, ideally case processing, database care, regular searches and resulting work, including the relevant EU portals. Active communication with customers as well as answering enquiries and managing projects of our customers will give you pleasure. You speak German and English fluently.

A motivated team with flat hierarchies and a very family-conscious working climate A collegial working atmosphere and a corporate culture in which it is fun to work and in which it is always openly communicated Depending on your personal needs, you can work in part or full time, depending on the project work, regular work in the home office is possible. Self-effective action with any cooperative support The possibility of configuring the growth of a medium-sized company and thus setting its own handwriting Many opportunities to act with our worldwide laboratories and companies in international projects Individual training and development opportunities Joint team events and leisure opportunities