DESIGN ASSESSOR/MANAGER - HOME BASED UK - SALARY NEGOTIABLE Line Manager’s Position: Clinical Affairs and Regulatory - Senior Manager Job Title: Flexible dep on Experience (DESIGN ASSESSOR/TECHNICAL MANAGER, etc.) Salary: Circa 65k with 20% performance based bonus Type: Permanent Location; Home based in UK, 1-2 days in Office per month & with travel Benefits: Company car, Healthcare, Pensi...
Superb, brand new opportunity for a competent Regulatory and Quality Affairs Manager to join this rapidly growing, global radiotherapy equipment developer. As an experienced Regulatory and Quality Affairs Manager you will assist in extending the company’s expansion into new markets and territories. The Company: Our highly successful North London based client is a fast growing 3D imaging medical technology company speci...
Regulatory Advice Manager - South East London Description We have an exciting opportunity for a Regulatory Advice Manager. You will be providing policy advice and guidance to all areas of the business in relation to FSA regulatory rules, guidance, and associated matters, including supporting relevant projects and processes, ensuring provision of business focused solutions. What does being a Regulatory ...
My client is a global Pharmaceutical company with a diverse and robust pipeline of products and who focus’ on the Research & Development of products in speciality area’s of unmet need. Due to continued expansion of they are looking to appoint a Medical Affairs Project Manager who will have a solid Project Management background in managing EU Studies, vendor management and a strong commercial acumen. Some of experience of working w...
Our client is an API and intermediate manufacturer based in Hertfordshire. They are currently looking for a Regulatory Affairs Officer to join their regulatory department. Responsibilities: - You will assist in the compilation, assembly and submission of Drug Master Files and Certificate of Suitability for our clients existing and new Active Pharmaceutical Ingredients. - To assist in...
This well established family owned Japanese Pharmaceutical business in Slough, that has seen rapid growth over the past year to eighteen months, is seeking an experienced Regulatory Affairs officer to help take them forward to the next stage of their development. Roles and Responsibility - Liaising with MHRA (Medicines and Healthcare products Regulatory Agency) and EMEA. - Obtain information of regulatory a...
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Date: 2 May
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Qatar,
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Salary negotiable
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3 applications
Pulse International is looking for a Manager for Pharmacy Regulatory Affairs for an exciting new healthcare project in Qatar. Scheduled to open in 2013, the Sidra Medical and Research centre will offer the latest technology and equipment to meet world-class standards in patient care, medical education and biomedical research. There will be a sophisticated clinical and translational research programme, general adult medical and surgi...
About Us From Huggies® diapers to Kleenex® facial tissues, Kimberly-Clark makes the essentials for a better life. Our 57,000 global employees are changing the world for the better with innovative products that create new categories and push existing ones to a higher level. While building our business, we’re also building careers through first-class education, engaging experiences and exposure to some of the world’s m...
About Us From Huggies® diapers to Kleenex® facial tissues, Kimberly-Clark makes the essentials for a better life. Our 57,000 global employees are changing the world for the better with innovative products that create new categories and push existing ones to a higher level. While building our business, we’re also building careers through first-class education, engaging experiences and exposure to some of the world’s m...
Organisation Description Leading global life sciences organisation Job Description This role requires a seasoned Regulatory Affairs Manager who has excellent people management skills. Based in Dubai you will manage a large team responsible for the registration of pharmaceutical products for all Gulf countries. As a key stakeholder you will ensure that products are regi...
• Information Manager with a background in the biological sciences • North London / Hertfordshire border based • Salary £28,000 - £30,000 + private health care and bonus scheme • Experience of electronic data management essential, Sharepoint or other document management systems an asset • Biological or Library Sciences graduate with experience in a pharmaceutical environment preferred • Global organisation...
Lab Solutions has an immediate need for a Regulatory Affairs Manager to join a global healthcare company.This role would entail day to day managing of the regulatory team, participating in new product introductions, ensuring products comply with national and European regulatory requirements, ensuring work is compliant with internal procedures.The candidate will have extensive experience managing/leading a team, high degree of technical comp...
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Date: 25 April
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France,
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€55,000 - €70,000 per annum, negotiable, pro-rata, inc benefits
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6 applications
SPINE PRODUCT SPECIALIST - MEDICAL DEVICES - FRANCE Job Title: EU Notified Body Medical Device Product Specialist Primary Report: Technology Team Leader NB 0086 Secondary Report: Local manager (TBC) Location: UK or France Type: Permanent Employment Purpose of Position Conduct Technical Reviews for medical device CE conformity assessment certification Manage a portfolio of ...
17 jobs matching this search were posted in the last week
SPINE PRODUCT SPECIALIST - MEDICAL DEVICES - UK Job Title: EU Notified Body Medical Device Product Specialist Primary Report: Technology Team Leader NB 0086 Secondary Report: Local manager (TBC) Location: UK or France Type: Permanent Employment Purpose of Position Conduct Technical Reviews for medical device CE conformity assessment certification Manage a portfolio of medi...
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Date: 18 April
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Abingdon, Oxfordshire
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£30,000 - £40,000 per annum, negotiable, pro-rata, inc benefits
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4 applications
SENIOR RA ASSOCIATE - Medical Devices - Oxfordshire - Circa 35-40k Type: Permanent Reports to: RA Manager Purpose: Provide Regulatory and Quality Assurance support to the business. To operate as a member of the RA team with a mandate to promote a regulatory sound business practice and support the continuous improvement ethic throughout the organisation. Responsibilities: Reporting duties to RA ...
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Date: 18 April
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China,
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£40,000 - £70,000 per annum, negotiable, pro-rata, inc benefits
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9 applications
PRODUCT SPECIALIST - MEDICAL DEVICES - CHINA - NEGOTIABLE Job Title: EU Notified Body Medical Device Product Specialist China Primary Report: Technology Team Leader NB 0086 Secondary Report: Local manager (TBC) Location: Shanghai/Shenzhen, China Type: Permanent Employment Purpose of Position Conduct Technical Reviews for medical device CE conformity assessment certification ...
European Regulatory Affairs Manager - Agrochemicals - North West - Registration Manager Our client is an established and global enterprise with a focus on specialised chemicals. As the leading producer of products within their chosen industry, you will be applying to a company with a phenomenal brand image that has the reputation for being the best. Association with such a company will contribute positively to your career progres...
QLAB, based in Livingston, is a central laboratory where clinical trial samples collected from patients are sent for analysis. Our world-class laboratory provides full analytical support for a huge variety of analytical techniques. Our team of Project Service staff organize, set up and run these clinical trials both regionally and globally. They are involved in all aspects of trials working alongside Finance, Contracts, Regulatory Affairs,...
Our client is a leading pharmaceuticals business, due to rapid growth and expansion we are recruiting for an experienced Regulatory Affair Manager to join the team based in exclusive West London offices. As Regulatory Affairs Manager you will have previous experience and a deep understanding of National Phase procedures. Key responsibilities: Submission of End of Procedure national phase documents for C...
Deputy QA Manager - Pharmaceutical - GMP/GLP - UKAS - Permanent - West London - £30-40k + 20% Bonus Are you an experienced pharmaceutical QA professional with strong knowledge of GMP / GLP? Are you looking for a new challenge offering superb career growth potential? A leading testing laboratory is currently seeking a Deputy QA Manager who, with the Head of QA, will lead the company's Quality Managemen...
Pharmaceutical Technical Project Manager - East Sussex Opportunity : This is a great opportunity for a Technical Manager or a Project Manager to join a leading pharmaceutical company where you will manage the full drug development projects from conception through to manufacture. You will work with clients on new product development as well as exiting products and manage the technology transfer. <...
Our client is a leading pharmaceuticals business, due to rapid growth and expansion we are recruiting for an experienced Regulatory Affair Manager to join the team based in exclusive West London offices. As Regulatory Affairs Manager you will have previous experience and a deep understanding of National Phase procedures. Key responsibilities: Submission of End of Procedure national phase documents for C...
Pharmaceutical Senior Compliance Manager - Croydon Opportunity : This is a great opportunity for someone who has good pharmaceutical quality assurance and regulatory affairs compliance experience to join a growing pharmaceutical manufacturing company in Croydon. Your role as a Senior Compliance Manager will involve leading and managing quality assurance, regulatory affairs and compliance projects. Th...
Pharmaceutical Senior Compliance Manager - Croydon Opportunity : This is a great opportunity for someone who has good pharmaceutical quality assurance and regulatory affairs compliance experience to join a growing pharmaceutical manufacturing company in Croydon. Your role as a Senior Compliance Manager will involve leading and managing quality assurance, regulatory affairs and compliance projects. Th...
Pharmaceutical Technical Project Manager - East Sussex Opportunity : This is a great opportunity for a Technical Manager or a Project Manager to join a leading pharmaceutical company where you will manage the full drug development projects from conception through to manufacture. You will work with clients on new product development as well as exiting products and manage the technology transfer. <...
