Are you looking to establish your regulatory affairs career with a top medical device company that will develop your skills on a global scale? If you answered yes ensure you apply for this regulatory affairs associate role today. Our client are looking for a regulatory affairs professional with some experience within the medical device industry, who has a good understanding of the technical documentation and ISO standards. Apply today to find out more!
Our client is a leading Biotech who have a year long contract for a Senior Regulatory Affairs Manager focussing on the EU market. The role will support one or more products from a regional regulatory perspective. ...
(Executive/Senior) Director - Oncology Collaboration
NonStop Recruitment are currently sourcing for on behalf of our client, a leading dental device company for a regulatory affairs manager. This role is part-time with around 50-80% work load. As the regulatory affairs manager in this role you will be in charge of the project management of global medical devices within the interesting and innovative area of dental products. Apply today to find out more about the flexibility and invaluable experience you can gain with this role!
Medical Director - Clinical Development (COPD/Asthma or Critical Care)
My client, a biotech company, is urgently seeking an experienced freelance CRA in Israel on a 2 year contract to be home based!
Indication: Stem Cell
* Assist in protocol feasibility analysis, clinical site identification and patient recruiting. * Oversee study start-up activities and maintain contact with investigators, CRO and study sites. * Perform on-site visits and source data verification of DCFs and CRFs. ...
Head of QA, China, Responsible for whole manufacturing site!
My client is one of the leaders in pharmaceutical production and development and they are looking to recruit a head of QA for one of their manufacturing sites. This role does require applicants to be fluent in Mandarin or Cantonese and have extensive experience in GMP quality assurance.
New opportunity due to growth within the company for an experienced manager within QA operations. In this role you will manage six qualified persons directly and be responsible for their teams, totalling 30 QA professionals. You will be joining a global leader at one of their key sites and be able to take on a great new position.
A new position has arisen within my client due to continued growth of the company, particularly the Swiss operations. You will be working alongside the quality assurance (QP) team focusing on release and distribution of products to the Swiss market. My client focuses on allergy products and is going through a period of sustained growth.
Switzerland, a country known for its beautiful sites and considered to be highly desirable location to live in. There is a leading global pharmaceutical company who is looking to recruit a Head of Quality Swiss QP to join their team in Switzerland. They have invested in their consumer care division and want to see it grow over time, giving you the chance to grow with the company.
Global Regulatory Affairs Manager â€“ Biologics â€“ Germany
As Global Regulatory Affairs Manager you will be in charge of leading a project team and working on various regulatory submissions. A strong focus will be on compiling and reviewing Module 3. Further, you will be responsible for strategic planning and implementing new regulatory guidelines. Additionally, you will be working with other departments and cooperates with different sites.
Regulatory Affairs Manager â€“ Global Scope â€“ Germany
As Regulatory Affairs Manager you will be in charge of leading a project team and working on various regulatory submissions. A strong focus will be on compiling and reviewing Module 3. Further, you will be responsible for strategic planning and implementing new regulatory guidelines. Additionally, you will be working with other departments and cooperates with different sites.
Clinical Trial Biostatistician - Global Nutrition - Lausanne
100,000CHF - 115,000CHF
This is a brilliant opportunity to work for a leading global nutrition, health and wellbeing company. My client is involved in pioneering research which enables people to live healthier lifestyles meaning your work with them really makes a difference.
Senior Clinical Programme Lead â€“ Oncology/Haematology
I am recruiting for a Senior Clinical Programme Lead to focus on the therapeutic area of oncology and haematology. This one of my client's main indications, and they have a well-established research dedicated solely to oncology. As a result, it is an area that the company has really invested, meaning that it is extremely well-funded. Due to this, the role comes with a lot of long term scope, leading to an interesting and career path full of potential.
Do you have sound experience with class III medical devices? And a technical/medical/scientific degree? In addition, solid knowledge of EU regulations as well as other countries' regulations? On top of this, you speak fluent German and English? And nonetheless, you have quality management experience? Then you have the right profile for the Vigilance & Post Market Surveillance Manager position within a growing and succesfull company.
A major biotechnology company based in Switzerland working in the field of drug therapy for inflammatory disorders. The company operates in more than 50 countries worldwide, distributing to major medical centres that use its advanced compounds in over 200 trials.
IT Business Analyst â€“ 2 year contract â€“ Global Pharma - Â£500 per day
The Hydrogen Group has been appointed to search and select a Senior Manager, Global Regulatory Project Leader on behalf of a large global pharmaceutical company that is present in more than 150 Countries in the world. The company has a growing portfolio of Innovative products in key therapeutic areas. They are currently looking for an experienced Regulatory Affairs professional to join their Global Regulatory Affairs team.
QP Head Of Quality - High Living Standards - Switzerland
A global pharmaceutical company located in Switzerland, a country known for its beautiful sites and high living standards, is looking for a Head of Quality Swiss QP to join their team in Switzerland. My client has invested in their consumer care division and seeks for talented individuals to help it grow.
* Manages overall operation of the entire clinical study including project planning, budget, resource management and CRO management * Directs the design, documentation, testing and implementation of clinical data collection studies, external reproducibility studies and clinical database review * Ensures GCP ICP regulatory compliance * Develop and manage clinical budget and contingency plans for clinical trials * Manage full scope of stud ...
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