26 English-speaking jobs in Morges

Overview Summary This position is responsible for working with the physicians and other clinical scientists within Early Clinical Development to provide clinical research support for early phase clinical programs as assigned by therapeutic area and type of therapy. Primary focus will be on I&I programs. Duties and Responsibilities Development of protocols for clinical studies.

Overview Summary You will become a member of a dynamic, proactive, innovative, enthusiastic team where everyone’s contribution counts. We enjoy working with like-minded colleagues who want to join forces and go the extra mile to improve the lives of patients and build sustainable operations in Europe and abroad.

DUTIES AND RESPONSIBILITIES Contribute to submission preparation activities with Incyte QA and Incyte CMOs, Perform initial gap assessment for QA documentation in preparation of GMP applications, Collect and maintain product submission data as well as country specific GMP accreditations for Incyte entities and partners, Support and closely collaborate with Incyte Regulatory affairs for MAAs activi

Sales Development Representative page is loaded Sales Development Representative Apply locations Tolochenaz, Switzerland time type Full time posted on Posted 2 Days Ago job requisition id JR100806 By joining Bio-Techne, you’ll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics.

Overview SUMMARY The Manager Commercial QA Packaging & Distribution is responsible for the Quality oversight of product distribution activities in multiple markets. He ultimately ensures that commercial products are distributed to end-customers in compliance with Incyte Quality standards and applicable regulations and GxP guidelines.

Salary: confidentiel We are seeking a knowledgeable and dependable Regional Tax Manager to join the tax team for one of our clients in Canton de Vaud. This role offers the opportunity to manage the company’s tax affairs across a large region. The successful candidate will have the chance to develop themselves professionally and explore different opportunities within the company.

Overview Job Summary The Associate Director, Principal Medical Writer I is responsible for the development of clinical documents for submissions to regulatory authorities globally.

Overview SUMMARY The Manager Commercial QA Packaging & Distribution is responsible for the Quality oversight of product distribution activities in multiple markets. He ultimately ensures that commercial products are distributed to end-customers in compliance with Incyte Quality standards and applicable regulations and GxP guidelines.

Overview Temporary position SUMMARY The Senior Specialist Global Distribution QA is a key contributor to the expansion of Incyte products in multiple markets. He/she ultimately ensures that commercial products are distributed to end-customers in compliance with Incyte Quality standards and applicable regulations and GxP guidelines.

Overview Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients, make a difference in health care, and build sustainable value.

Aperçu Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients, make a difference in health care, and build sustainable value.

Overview Summary This position is responsible for working with the physicians and other clinical scientists within Early Clinical Development to provide clinical research support for early phase clinical programs as assigned by therapeutic area and type of therapy. Therapeutic areas include immunology, hematology and oncology.

Overview Summary You will be part of a dynamic, proactive, and innovative team where everyone’s contribution matters. We value working with like-minded colleagues who share a commitment to improving patients' lives and building sustainable operations internationally.

At Accuray, we make a direct and powerful impact on the lives of cancer patients every day — helping them live longer, better lives.

about the role Some highlights Being part of an international company yet with local presence Build a safer digital society together with us Working as aServiceNow Lead Architect We are looking for a ServiceNow Lead Architect who embodies a challenger mentality, ready to own and drive platform innovation while shaping strategic outcomes for our ServiceNow ecosystem.

As the Finance Director at Kainjoo Consulting Group, you will oversee all the company’s financial aspects. In addition, you will provide financial guidance, develop financial strategies, and manage a team of financial professionals to ensure the company’s economic success.

Kainjoo Consulting Group is seeking an experienced Human Resources Manager to oversee all aspects of HR operations. The ideal candidate will develop and implement HR strategies, policies, and programs that align with the company’s goals and objectives. They will also ensure compliance with all federal, state, and local regulations related to HR.

Overview Summary The Sr Manager, Regulatory Affairs, CMC will primarily be responsible for supporting / managing regulatory CMC submissions and strategy for Incyte development and marketed products, including both small molecules and biologics, from early development through late-stage (phase 3, registration and post-approval).

Overview Summary The Sr Manager, Regulatory Affairs, CMC will primarily be responsible for supporting / managing regulatory CMC submissions and strategy for Incyte development and marketed products, including both small molecules and biologics, from early development through late-stage (phase 3, registration and post-approval).

Overview Summary Responsibility for managing and maintaining existing development and marketing authorization dossiers and compiling submissions in compliance with ICH specifications and Health Authority regulations globally.