Our client is a global pharmaceutical company with exciting compounds in their product pipeline. This company, with offices in Switzerland, require a Medical Affairs Manager for the activities associated to a Multiple Sclerosis drug moving into late phase development and into the open market. ...
Validation Engineer - 6 Month Contract - South East
A Global based Bio -Pharmaceutical Company are looking for a Validation Engineer to join their team on an initial 6 month contract. They are looking for someone on a 1.0 FTE basis working in their Slough office assisting them with their Validation project. The company are looking for someone with varied experience throughout Equipment.
Great company with attractive package and benefits in a prestigious working environment
Director, Global Clinical Development- Respiratory
Company:Hays Life Sciences Location: South West England Salary: 100,000+ Benefits: car, bonus, pension
Closing Date: 16 Oct 14
Fantastic opportunity to join a growing Biopharma with strong plans for growth over the next two years. This role is responsible for developing the Global clinical development strategy for an upcoming respiratory portfolio tipped for big things.
You will lead global clinical and regulatory teams to guide the strategy of these respiratory drug development programmes through regulatory drug development in the U.S. & Europe.
Medical Director CNS – Early to late clinical development
I am recruiting for a Medical Director, CNS, to focus on early clinical development through to the late phases. You will be fully involved with international study design and driving the development strategy, as well as leading a multi-disciplinary, multi-regional, matrix team. They are looking for someone with sound experience in phases I-II in particular, with solid TA knowledge. The company has several different compounds in psychiatry, creating a promising pipeline and an exciting future!
I am recruiting for a Medical Director, CNS/Psychiatry on behalf of a company that is truly research driven. They are looking for someone with deep knowledge in CNS and with sound extensive in clinical development. You will be fully involved with international study design and driving the development strategy, as well as leading a multi-disciplinary, multi-regional, matrix team. The company has several different compounds in psychiatry, creating a promising pipeline and an exciting future!
A leading medical device and family run company specialising in endoscopic devices are actively looking for a Sales Specialist experienced in the medical technology field to work with their complete range of minimal invasive surgical devices across the Germanic and Italian regions of Switzerland (Schweiz).
Senior Global Marketing Director
Salary: £130,000 + excellent benefits package
A fantastic opportunity for an enthusiastic and confident marketing professional to take their career to the next level and work for a large global pharmaceutical company.
Statistical Consultant, Long Term Contract, Germany
SEC Pharma is proud to working on behalf of an industry renowned pharmaceutical company. This is a very rare and exciting opportunity for a statistical consultant to join an innovative and forward thinking company on a very long term contract. A 24 month contract is on offer along with a very competitive hourly rate.
In summary, your role as a statistical consultant will be to provide statistical and programming support to the project statisticians in the group.
I am currently recruiting for a Supplier Quality Engineer, for a leading Medical Devices company! This is a 3 Months contract, with high rates, giving the opportunity to get some extra income before Christmas!
This leading pharma is looking for a Senior Manager in Regulatory Operations / Publishing on a 6 month contracting basis.
As Senior Manager within Regulatory Operations / Publishing you will be responsible for managing, planning and leading all document management activities required to publish high quality regulatory submissions and clinical study reports
This is a fantastic opportunity within a world leading medical device company to develop the QMS and registration process on a local scale. Our client are looking for regulatory affairs and quality assurance professionals from the medical device industry who have the tenacity to develop their department, working on class I through to class III products. Apply now to find out more.
English & Italian Speaking Technical Writer – Medical Devices – Ticino
A well established biotechnology company with a strong reputation in the Swiss market are currently searching for an Applications Specialist to join their commercial teams as a technical link between external collaborators and internal projects.
To lead the Quality Assurance function at the site. Engage with the site leadership, delivering the site business goals and QA strategy. To implement quality systems across the site to ensure the quality of finished goods provided by the site. To play a leading role in the leadership team, ensuring that Quality Assurance is integrated into all of the relevant site activities. To provide leadership and development of the individuals and teams.
Document Control SME - 6 Month Contract - Med Device - IL
Training and Document Control SME - 6 Month Contract - Med Device - Chicago
My client, a Chicago are based Medical Device company is looking for a SME for Document Control/Training. This is fantastic opportunity to join a growing Medical Device company. My Client is looking for an experienced individual who has excellent experience in Document Control and training.
Senior CRA – International Travel – Italy, Spain and Germany
Senior CRA - International Travel - Italy, Spain and Germany
A client in Switzerland is looking for a Freelance Senior Clinical Research Associate to travel to sites in Europe. The vacancy is for a SCRA to be field-based, travelling to sites mainly in Italy but also in Germany and Spain. This opening is offering a flexible contract, where you can travel and work from home and gain valuable experience.
Real Pharma is looking for a VP of Technology to join a Managed Markets Agency in New Jersey. If you have a background that combines both technological and creative aspects, and you are interested in being the #2 person in the digital group, then this position is for you!
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