Emploi Associate director regulatory cmc biologics Suisse

 ...inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as an Associate Director, Global Regulatory Affairs CMC - Marketed Products in our Zurich office. Here, everyone matters and you will be a vital contributor to our... 

 ...Marketing team and bring your passion and talent to work.  Associate Director Integrated Marketing    Männedorf, Switzerland   Your...  ...reference letters and diplomas are optional).   #lifescience #healthcare #automation #medicaldevice #biology #biotechnology... 

 ...pharmaceutical company based in Canton de Neuchâtel Quality Control Associate Director H/F Guide, mentor & develop your teams to achieve an...  ...tracking of all compliance activities (GxP as well as other regulatory requirements). Including: Accountable for the departments... 

Joining CSL as Associate Director Global Feasibility offers an exciting opportunity to be part of a continually growing team dedicated to the...  ...and collaborate with internal functional area leads (e.g. Regulatory Affairs, Clinical Vaccine Group) to build knowledge on study... 

 ...WuXi values and competencies.   Job Summary:   The Associate Director Quality Contro l is charged with Overseeing the Quality...  ...tracking of all compliance activities (GxP as well as other regulatory requirements). Including: Accountable for the departments... 

 ...develop and support your team associates in their professional growth...  .... Our team develops Biologics drug substance and drug products...  ...responsibilities As Associate Director you will lead the Method...  ...assurance, scientific office, and regulatory affairs, e.g. to ensure... 

 ...a challenging and rewarding career in biologics drug product development? Do you want to...  ...budgets (internal and external costs) and regulatory requirements. Engage with internal...  ...this? With our people. It is our associates that drive us each day to reach our ambitions... 

 ...offices in Geneva, Shanghai, and sales office in New York. WHAT YOU’LL DO DLG seeks a Strategic Planning and Research Associate Director with proven luxury and lifestyle expertise and a digital-first mindset. You will strengthen and promote some of our critical... 

 ...client based in the canton of Vaud is currently seeking a Biologics QA Manager to strengthen their team following an increase...  ...-up with concerned CMOs. - Provide QA support to the RA-CMC group for regulatory submissions and follow-ups. - Implement Quality Risk Management... 

 ...) requirements Collaborate with CMC Development teams, Regulatory Affairs and Quality functions to co...  ...the many variables and uncertainties associated with the biosimilar business....  ...biosimilar products (preferably) and/or New Biological Entities in the EU/US... 

 ...further support with the growing CMC activities we seek to recruit...  ...report CMC project status to Director CMC and project teams...  ...documentation in compliance with regulatory requirements by FDA, EMA, and...  ...Biotechnology, Biochemistry, cell Biology or equivalent is required)... 

 ...Reporting to VP, External Biologics Manufacturing, this position...  ...will work closely with the Director, External QC Commercial Biologics...  ..., Quality Assurance and Regulatory CMC groups to support product specifications...  ...Incyte CPV and APQR reports associated with external commercial... 

 ...changing. Those aren't words that are usually associated with a job. But working at Bristol Myers...  ...Master's degree in biochemistry, biology, microbiology, chemistry, engineering, pharmacy...  ...performed in accordance with approved regulatory submissions, technical agreements, and... 

 ...the innovative renewal of this capability. As Data Modelling Product Manager, you will lead our global Data Modelling Product and associated matrix team to further increase its value to drug discovery and will engage with key business and RX stakeholders to identify and... 

Overview: Summary   Reporting to the Business Lead IAI, Region Europe and member of the IAI EU Core Team. Leads, develops and executes marketing strategy & activities for Opzelura (Ruxolitinib Cream) in close alignment with GPS, Commercial Operations, Medical Affairs...

 ...CMC Project Manager (m/f/d) Standort: Düsseldorf, NW, DE, 40468 | Werne, NW, DE, 59368 | Goettingen, NI, DE, 37081 |...  ...site organization. The role of CMC Project Manager reports to the Director CMC – Pharmaceutical Development and deals with projects in the... 

 ...About the role The Associate Director, Global Program Management, Oncology, will provide project management expertise as an individual contributor to early-stage drug development programs. The key to success will include working across a global team, building impactful... 

 ...frictionless user experience. As an Associate Director Product Growth Manager you flexibly...  ...ensure adherence to security, quality, and regulatory standards and policies, including GxP...  ...discovery scientific field such as biology, chemistry, computational sciences or... 

Our client based in the canton of Vaud is currently seeking a Biologics QA Manager to strengthen their team following an increase in activity. This assignment will be for a minimum duration of 6 months due to the company's growth.This person will oversee the quality of...