Mein Kunde, ein internationales Unternehmen mit Sitz in Hessen, sucht eine/n Director Regulatory Affairs. Diese Position ist eine Leitungsposition und Sie sind fĂĽr ein Team von 8-10 Mitarbeitern zustĂ¤ndig. Dies gibt die MĂ¶glichkeit gibt, ein Team zu leiten. Weiterhin sind Sie aktiv an der Einstellung neuer Mitarbeiter beteiligt, was Ihnen die MĂ¶glichkeit erĂ¶ffnet, neue Erfahrungen zu erlangen.
We currently have a freelance created opportunity for a Medical Scientists to join the International Haematology/Oncology Therapeutic Area, supporting phase I-II clinical development. This is a full time interim contract with a global pharmaceutical company in the Basel region.
Regulatory Affairs Associate Director, Zug, International Role, Focus for Regulatory Compliance
Sr. SAS Programmer
Company:Real Staffing Location: South San Francisco Salary: 100,000+
Closing Date: 14 May 14
An outstanding and highly coveted Biopharmaceutical company in the San Francisco Bay Area is looking to bring on a Sr. Statistical Programmer to join their experienced group. This is a full-time, onsite role.
* Acts as lead statistical programmer for a project. * May participate in sub-team meetings as a representative of Statistical Programming group. * Provides consistency and quality assurance across various studies. ...
Global Regulatory Affairs Director - Switzerland - Emerging Markets
My client is a leading Pharmaceutical company with a long pipeline, offering great projects in varied therapeutic fields. This gives you the unique opportunity to grow into a Global RA liaison with strategic responsibility for development and registration projects. This role will see you quickly become an industry expert in a unique line of products and see you become one of the important figures in the company.
SEC Pharma is closely working with global pharmaceutical company who is consistently driving research and innovation to help consumers all around the world to live a better life. To strengthen their Quality Department, we are currently looking for a:
Global Director of Supplier Quality - Pharma Division
A leading medical device company based in the Zurich area that produce world leading and innovative diagnostics are looking for a regulatory affairs manager to join their team. Our client are looking for a regulatory affairs professional with several years of experience within the medical device industry. You will gain an international role with great prospects of leading a team and developing the regulatory affairs department in the future. Apply today to find out more!
Joining this healthcare company at an exciting time of expansion will see you entering into a global team and participating in team events and meetings on a European level. This is a fairly junior position that will strongly elevate your reputation within the Swiss medical device market and give you the change to join a globally successful organisation, as well as becoming part of a dynamic sales force that provide a support network on an international level.
Apply today for a regulatory affairs associate role within a growing and developing medical device company based in the Bern area. If you are looking to develop your regulatory affairs career with a company at their exciting point of growth then ensure you apply today to find out more about the innovative medical devices, career progression and interesting role you will gain. If you are a regulatory affairs professional within the medical device industry we want to hear from you today!
An excellent job opportunity has come up with one of the medium sized pharmaceutical companies based in Germany. The Pricing and Reimbursement department are looking for a manager to join their team. This is an excellent opportunity for somebody coming from the consultancy field to join a fast growing, dynamic company and develop their skills further! You will be working alongside a highly experienced Director on international level!
Director of Marketing - 10+ years experience, previous speciality care (Step up from Marketing Manager)
One of the most renowned companies in the pharmaceutical industry is seeking an experienced industry physician to join them based in Germany - helping to lead their global clinical development projects.
This is a unique opportunity to be involved in the preparation of regulatory strategy for a range of non Pharma products which are currently in pre clinical stages. This role will see you quickly become an industry expert in a unique line of products and see you become one of the 'go to' people in the company. My client is a leader in their field, renown for having a dynamic and flexible environment where to top it off, you can expect above average s
Director Regulatory Affairs â€“ FĂĽhrungsverantwortung â€“ Hessen
Mein Kunde, ein internationales Unternehmen mit Sitz in Hessen, sucht eine/n Director Regulatory Affairs. In dieser Position haben Sie FĂĽhrungsverantwortung, was Ihnen die MĂ¶glichkeit gibt, ein Team zu leiten. Weiterhin sind Sie aktiv an der Einstellung neuer Mitarbeiter beteiligt, was Ihnen die MĂ¶glichkeit erĂ¶ffnet, neue Erfahrungen zu erlangen.
We are currently looking for an experience clinical and epidemiology statistics specialist to join a large team of informatics and statistics specialists in the Bern area. You will be acting as statistical advisor for the product development department for a variety of projects explaining statistical concepts to the team and incorporating important findings into the development of new products. ...
Amazing oppotunity to work for one oof the top 5 pharmaceutical companies where your role will be to assist with the activities relating to the Labelling Compliance Review. Deliver to time and quality targets as defined by the project
Our global Pharmaceutical client is looking for an experienced Business Development Lead to agree business requirements across diverse groups of stakeholders, design and deliver solution business service design and implementation.
Director Regulatory Affairs â€“ Internationales Unternehmen
Als Director Regulatory Affairs sind Sie fĂĽr die Leitung der Zulassungsabteilung im Bereich Tiermedizin zustĂ¤ndig. Weiterhin ĂĽberwachen und leiten Sie die Erstellung und Erhaltung der CMC Dokumentationen. Weiterhin stehen Sie in Kontakt mit den zustĂ¤ndigen BehĂ¶rden und reprĂ¤sentieren das Unternehmen.
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