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Earth/Environmental Sciences Jobs in Hertfordshire

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Associate Documentation Specialist

Salary:
Competitive
Location:
Hertfordshire
Job Type:
Permanent
Date Posted:
24-May-2012 09:16Add to My Shortlist

JOB SUMMARY Supports Medical Writers and Regulatory Affairs authors to ensure data accuracy and formal quality in the documentation used in Clinical Studies and Regulatory Submissions. BACKGROUND Our client is one of the world's leading research-based pharmaceutical companies with operations in the U.S., Asia, and Europe, they employ more than 11,000 people worldwide. PRIMARY DUTIES * Under supervision of the Senior...


Senior Regulatory Affairs Consultant - CMC

Salary:
£25 - £60 p hour
Location:
Hertfordshire
Job Type:
Contract/Interim
Date Posted:
24-May-2012 00:00Add to My Shortlist

A Global Pharma company are presently looking to bring in a Senior Regulatory Affairs Consultant to their CMC group, within the EU team to be based in the UK West London Office, on a contract basis. Role: - Preparation of high quality, chemistry manufacturing and control (CMC) detailed regulatory documents using varied information sources. - Liaising closely with other personnel to...


Senior Structural Engineer

Salary:
£35k - £45k pa + package
Location:
St, Albans
Job Type:
Permanent
Date Posted:
25-May-2012 09:07Add to My Shortlist

Senior Structural Engineer Hertfordshire £35,000 to £45,000 Are you a chartered engineer or approaching your chartership status? Are you looking for a position that can offer you excellent career progression whilst working on a wide variety of projects? If so, then please read on. This client provides a multi-disciplinary service in areas including Structural and Civil Engineering, Building Surveying, Land...


Project Engineer (Environmental Test) x2

Salary:
35000.00 - 40000.00 GBP Annual + GBP35000 to GBP40
Location:
Hertfordshire, Not Specified
Job Type:
Permanent
Date Posted:
30-May-2012 00:00Add to My Shortlist

Position: Environmental (Test) & Project Engineer x 2 Location: Hertfordshire Duration: Permanent Salary: TBC Circa GBP35,000 - GBP40,000 p/a plus excellent benefits The Company An exciting opportunity to work with my client who are a leader within the Defence Sector specialising in providing UK, Europe and Global anti-war deterrents. They offer a state of the art manufacturing facility who utilise...


Manager Clinical Operations and Compliance, SOCS CFU

Salary:
On Application
Location:
Hertfordshire, London
Job Type:
Permanent
Date Posted:
26-May-2012 00:00Add to My Shortlist

BENEFITS: Flexibility to work from home, pension, bonus JOB SUMMARY: Our client is a top tier pharmaceutical organisation based in Hertfordshire. This is a unique role which will combine your knowledge of Clinical Operations, Drug Safety and implementing and managing process. You have strong leadership capabilities with the ability to provide direction for these processes through direct line management of... related issues. * Measure of success would include a positive impact on clinical trial timelines and/or controlled document, training, TMF or SUSAR issues. In addition, establishing innovative methods to streamline or combine activities which facilitate the quality of study trial documentation QUALIFICATIONS / EXPERIENCE REQUIRED: A bachelors in Science or health related discipline. KEYWORDS: Study Trial Administrator, CRA, SCRA, Senior CRA, Drug Safety, Clinical Operations Compliance TO APPLY: For a confidential discussion please telephone at AXESS Limited on 020 8560 2300. To apply, please send your CV to jobs@axess.co.uk quoting reference 5071 Only candidates with EU work authorisation will be considered....


Materials Officer - Tin

Salary:
£23k pa
Location:
Hatfield, Hemel Hempstead, St, Albans, Watford, Hertfordshire
Job Type:
Permanent
Date Posted:
23-May-2012 16:23Add to My Shortlist

My client is a unique focal point for the global tin producing and using industries, and, although originally a research based organisation, the activities of ITRI are increasingly influenced by issues of sustainability, for example, consideration of toxicological, environmental, health and safety, or social and community related concerns. Effectively managing these issues also requires us to understand the complete life cycle of tin from production, through use as a metal, alloy, or tin chemical, to end-of-life treatment and recycling or other forms of recovery. They are currently recruiting for a...


Associate, Clinical Trial Supplies

Salary:
On Application
Location:
Hertfordshire, London, Middlesex, Buckinghamshire
Job Type:
Permanent
Date Posted:
26-May-2012 00:00Add to My Shortlist

JOB SUMMARY: To coordinate, under supervisory direction, IMP packaging, labeling, distribution and accountability activities contributing to the on-time delivery of quality-driven clinical supplies. To collaborate with clinical supply team colleagues and external vendors in the creation of value within the overall clinical development process. PRIMARY DUTIES: Main duties/responsibilities: * Coordinate, under supervisory direction, IMP packaging and labeling activities * Work... at AXESS Limited on 020 8560 2300. To apply, please send your CV to jobs@axess.co.uk quoting reference 5184 . Only candidates with EU work authorisation will be considered. ABOUT AXESS: AXESS has been operating since 1990 We are a recruitment business dedicated to the pharmaceutical industry, specialising in Medical Affairs, Regulatory Affairs & Clinical Development We match professional candidates to the best permanent, contract and interim roles in the market Visit us at [URL removed]


Associate Director Clinical Operations Neuroscience

Salary:
On Application
Location:
Cambridgeshire, Essex, Hertfordshire, London, Middlesex
Job Type:
Permanent
Date Posted:
24-May-2012 09:14Add to My Shortlist

JOB SUMMARY: Rare opportunity for a Senior Project Manager/Programme Manager looking to progress into an Associate Director role within a top tier Pharma Company. This role will involve both strategic and scientific leadership for assigned studies and/or have overall Clinical Operations responsibility for a specified compound within the Neuroscience portfolio. May also have responsibility for direct reports, including hiring and development. BACKGROUND: Top Tier Pharmaceutical company based in Hertfordshire PRIMARY DUTIES: * Ensuring that Clinical Operations activities for the assigned projects proceed...


Regulatory Officer

Salary:
£40, 000
Location:
Essex, London, Hertfordshire, Cambridgeshire
Job Type:
Permanent
Date Posted:
25-May-2012 16:48Add to My Shortlist

An exciting opportunity has arisen for a Regulatory Officer within the European Regulatory Affairs Team. The focus of the role will be submission of new generic Marketing Authorisation Applications for retail products via the Centralised , Decentralised, or Mutual Recognition Procedures. There will be involvement in post approval support for critical pre-launch variations for European Procedures and a limited degree of renewals. You will...


EU Regulatory Affairs Manager

Salary:
On Application
Location:
London, Berkshire, Buckinghamshire, Hertfordshire, Surrey
Job Type:
Contract/Interim
Date Posted:
25-May-2012 09:05Add to My Shortlist

Benefits: Competitive Daily Fee JOB SUMMARY Responsible for the regulatory lead for a marketed product licensed through the Centralised Procedure coupled with supporting the preparation of an MAA for a product currently in Phase III. BACKGROUND Global Specialist Pharmaceutical Company Office Based Role within EU R&D Headquarters PRIMARY DUTIES In this role you will have two main responsibilities. Firstly, to... delivering results. TO APPLY: For a confidential discussion please telephone Omar de Bary at AXESS Limited on 020 8560 2300. To apply, please send your CV to jobs@axess.co.uk quoting reference 5202. Only candidates with EU work authorisation will be considered. Keywords: Regulatory Contract / / Regulatory Project Manager / EU Regulatory Affairs Manager / London / London / London / London / Interim / interim / contractor / contract / Regulatory Affairs jobs / careers / vacancies / positions / RA AD / Associate Director Regulatory Affairs / CARDIOVASCULAR / cardiovascular ABOUT AXESS: AXESS has been operating since 1990 We are a recruitment business...


Medical Assessor - Product Safety, Europe

Salary:
On Application
Location:
Cambridgeshire, Buckinghamshire, Essex, Hertfordshire, London
Job Type:
Permanent
Date Posted:
24-May-2012 09:15Add to My Shortlist

Benefits: Corporate Package JOB SUMMARY Excellent opportunity for a UK GMC registered physician looking to join a leading global pharmaceutical company. Based within the EU HQ you will contribute to the provision of a fist class Pharmacovigilance service by undertaking comprehensive medical evaluation of individual case safety reports (both spontaneous and clinical trial) and supporting the General Safety Officers (GSO)... quoting reference 5230. Only candidates with EU work authorisation will be considered. Keywords: Pharmaceutical Physician, Medical Assessor, Product Safety, Hertfordshire, PV Physician, Pharmacovigilance, Drug Safety Physician, Medical Review ABOUT AXESS: AXESS has been operating since 1990 We are a recruitment business dedicated to the pharmaceutical industry, specialising in Medical Affairs, Regulatory Affairs & Clinical Development We match professional candidates to the best permanent, contract and interim roles in the market Visit us at [URL removed]


Regulatory Documentation Scientist

Salary:
On Application
Location:
Essex, Hertfordshire, London, Middlesex
Job Type:
Permanent
Date Posted:
24-May-2012 09:14Add to My Shortlist

JOB SUMMARY: Here is a great opportunity to combine your scientific knowledge and writing skills in an important role with one of the world's leading healthcare companies. You will be responsible for the project management and preparation of vital safety regulatory reports for innovative products and part of a global team driving the development of our clients rich pipeline of new...


Senior EU Study Manager (Oncology)

Salary:
On Application
Location:
Berkshire, Buckinghamshire, Hertfordshire, Surrey, London, Middlesex
Job Type:
Permanent
Date Posted:
24-May-2012 09:16Add to My Shortlist

JOB SUMMARY: Senior Study Management of Phase II and Phase III Oncology studies according to ICH guidelines in support of the clinical strategies defined in the Integrated Development Plan (IDP) as they relate to European specific responsibilities. Support of Phase I trials may also be required. Office based from London HQ. BACKGROUND: Expanding Global Pharmaceutical Company EU HQ based in... Bary at AXESS Limited on 020 8560 2300. To apply, please send your CV to jobs@axess.co.uk quoting reference 5213. Only candidates with EU work authorisation will be considered. ABOUT AXESS: AXESS has been operating since 1990 We are a recruitment business dedicated to the pharmaceutical industry, specialising in Medical Affairs, Regulatory Affairs & Clinical Development We match professional candidates to the best permanent, contract and interim roles in the market Visit us at [URL removed]


UK- Medical Device Regulatory Affairs Associate

Salary:
On application
Location:
London, Bedfordshire, Hertfordshire, Buckinghamshire, Cambridgeshire, England
Job Type:
Contract/Interim
Date Posted:
30-May-2012 10:51Add to My Shortlist

Novella Clinical is a global, full service CRO with European Headquarters in Hertfordshire, England. We are committed to providing a superior service to our global clients, and as such we are seeking hire an experienced Regulatory Affairs Associate with a proven track record working in regulatory affairs and quality assurance in the UK or EU. The main responsibilities in this role will be to provide regulatory and quality support to select clinical research projects involving medical devices, Combination Products and Diagnostics. Working with the Director, Clinical Monitoring EU...


Regulatory Affairs Associate

Salary:
On Application
Location:
London, Bedfordshire, Hertfordshire, Buckinghamshire, Cambridgeshire, England
Job Type:
Permanent
Date Posted:
25-May-2012 00:00Add to My Shortlist

Novella Clinical is a global, full service CRO with European Headquarters in Hertfordshire, England. We are committed to providing a superior service to our global clients, and as such we are seeking hire an experienced Regulatory Affairs Associate with a proven track record working in regulatory affairs and quality assurance in the UK or EU. The main responsibilities in this role will be to provide regulatory and quality support to select clinical research projects involving investigational or marketed drugs, devices, biologics, or new medical procedures. Work with the...


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