Our client is a small Medical Device manufacturer based in Tuttlingen. They are looking to strengthen their RA & QA department to keep all new and existing medical device products compliant with the new MDR as well as bringing new innovative products to market. The role will cover products in all lifecycle stages, from early […]
Read moreAbout – Here at Scienta we are teaming up with a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. They are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. The QC ...
Read moreCompany Our client is an international medical device manufacturer focused on bringing innovative solutions to market, giving millions of patients access to the best care and healthier living. This is a fantastic opportunity to expand your career in a high growth business, where your unique skills are valued. They are looking for a Site Head […]
Read moreOur client is a international Medical Device company focused on innovation and digitisation, they are also a market leader with a well-established reputation in their field. Their mission is bringing cutting edge technology to market, giving millions of hospitals and laboratories access to the best equipment and facilitate their research and healthcare capabilities. This is […]
Read moreSr. Manager/ Associate Director Regulatory CMC – Small Molecule Want to join a Global Pharmaceutical leader? This client is a Global Bio-pharmaceutical Company focused on delivering high quality treatments to patients. They have a robust pipeline of development products and 9 commercial stage assets. Responsibilities: Provide regulatory strategic and/or operational support for Small-Molec...
Read moreMy client is a listed clinical phase biotechnology looking for a strong & established Head of Regulatory to join their growing organisation. As a Head of Regulatory you will have the following responsibilities: Provide leadership and hands on management of Regulatory Affairs their clinical and preclinical development portfolio, including CMC. You will work as the […]
Read morePosition Responsibilities Participate on project development teams and represent regulatory affairs by supporting project and product teams. Prepare regulatory submissions as required for global approvals for in vitro diagnostic (IVD) products, including preparation of reports and interaction with regulatory officials as required. Prepare and submit to notified body Technical Documentation need...
Read moreHead of Regulatory Affairs Want to join a growing biotech? This is a great opportunity for a Senior Regulatory expert to lead regulatory at Clinical Stage Immunology focused company. This client is seeking a hands-on head of Regulatory Affairs who will bring broad experience in regulatory affairs and operations along with a roll up the […]
Read moreCompany Regulatory Consultancy About Scienta are proud to be supporting an impressive, full service regulatory consultancy in Munich with a focus on drug development in Europe and the US. Role The role requires at least 15 years of Regulatory CMC experience, or technical CMC development experience in either Small Molecule or Biologic, or cell/gene therapy […]
Read moreMy client is a privately held Belgium-based respiratory company focused on the development of pharmaceutical products with superior clinical performance based upon differentiated technology delivered by their next generation Soft Mist Inhalation device to the lungs. As a Regulatory Senior Manager you will have the following responsibilities: Reporting to the Head of Regulatory, you’re res...
Read moreWant to join a global pharmaceutical leader as key member of the Advertising/Promotions and Labeling team? This is your chance! The Role: The Senior Manager, GRS, Advertising, Labeling, & Promotion will be responsible for the review and submission of creative and compliant advertising and promotion materials for our commercial oncology and hematology portfolio. Responsibilities: Serves [&he...
Read moreResponsibilities Oversee the day-to-day operations and manage project workloads throughout the team. Provide regulatory guidance on IVDD, ensuring necessary compliance to both local and international requirements. Adapt and implement regulatory strategies dependant on requests and changes in requirements (eg. new standards and guidelines). Responsible for liaising with notified bodies and regul...
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