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!
My client a global biotech company who currently have leading products for the treatment of neurodegenerative, hematologic and autoimmune diseases, who also employ over 10,000 professionals worldwide are currently seeking to bring on board a Director of Biostatistics to join their offices in Switzerland. ...
Senior CRA – Freelance position – Italy, Spain and Germany
Senior CRA - Freelance position - Italy, Spain and Germany
We are recruiting for Senior Clinical Research Associates with 5+ years of experience to work in Geneva. This SCRA contract role will take approximately up to 0.5 FTE, and so you will be able to control your hours more as a contractor. As a freelancer you can build your CV with an upcoming company and have more time to plan for yourself.
Clinical Trial Manager
Company:Real Life Sciences Location: South San Francisco Salary: 100,000+ Benefits: negotiable
Closing Date: 14 Oct 14
* Manages the operational aspects of clinical trials * Manages the study project plan, including timeline, budget, and resources * Participates in study strategy development, protocol, CRF development, Clinical Study Report preparation, NDA submission, as appropriate * Prepares metrics and updates for management, as assigned * Proactively identifies potential study issues/risks and recommends/implements solutions * Participates in and fa ...
An innovative medical device consultancy company based in the German speaking part of Switzerland are currently searching for a research and development engineer to join them on the innovation of a new technology. Be part of the future success the role will give you the opportunity to grow within the company and become successful leading to higher work fulfilment.
Are you a Device Engineer looking to work for worldwide specialized consultancy company? This unique opportunity will give you the security of a permanent position but the variety to work on various projects. My client is searching for a Device Engineer to join them on a permanent basis.
Senior Manager Regulatory Advertisement and Promotion
The Associate Director of Strategic Project Management is a pivotal position with high visibility across multiple cross functional areas. This individual is responsible from strategic project management specifically focussed on the transition of compounds from late stage R&D, drawing lead candidates into FTIM studies and early phase development. ...
An exciting position has become available working as a Contract Qualified Person with a global pharmaceutical company based in the South East. This will be responsible for releasing a variety of dosage forms and it will be possible to complete the role on a part time basis.
It is a pre-requisite to be a Qualified Person under the permanent provisions Directive 2001/83/EC.
Our client is a renowned pharmaceutical company with strong pipeline of projects that require an experienced Interim to Project Manage cross functional relationships and assist with the delivery of programs throughout phase I-IV development. ...
**Associate Director GCP/PV Quality - Leading Global Pharmaceutical Company - NEW YORK**
I am working with a Globally recognised and extremely successful pharmaceutical company, based in New York USA, who are actively seeking an Associate Director GCP/PV Quality Assurance and Auditing. The company can offer an excellent salary, benefits, plus they work in some very interesting areas of the industry. This opportunity will ideally suit a Senior Manager/Audit professional who has specialised in GCP and PV for the majority of their career.
**Associate Director GLP Quality Auditing** - Excellent Pharmaceutical Company, NY USA
I am working with a Globally recognised and extremely successful pharmaceutical company, based in New York USA, who are actively seeking an Associate Director GLP Quality Auditing. The company can offer an excellent salary, benefits, plus they work in some very interesting areas of the industry. This opportunity will ideally suit a Senior Manager/Audit professional who has specialised in GLP for the majority of their career.
* Strong skills in embedded software architecture and C programming * Knowledge of real-time operating systems, digital signal processing and digital control * Solid grasp of good hardware and software engineering practices * Proficiency with Verilog or VHDL for FPGA development * Proficiency with Matlab/Simulink and LabView * Track record of getting amazing products to market on time with fantastic innovati ...
Are you a Project Manager with experience within Human Factors? My client a worldwide specialized consultancy company are searching for a Human Factor Project Manager to join them on a permanent basis.
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