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Earth/Environmental Sciences Jobs in Surrey

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Regulatory Officer

Salary:
£34k - £35k pa + Full Benefits Package
Location:
Camberley
Job Type:
Permanent
Date Posted:
28-May-2012 16:40Add to My Shortlist

As the global leader in the ophthalmic marketplace, we are proud to meet the eye care needs of millions of people worldwide. For over 60 years, we have developed, produced and marketed the most advanced products available in ophthalmology. Dedicated to the provision of not only the highest quality eye care products, but to also making significant contributions towards the... We continue to grow from strength to strength and have recently been united with a leading eye care company to create a dedicated and focussed eye care business offering the widest spectrum of eye care products, serving the full life cycle of patient needs. In close collaboration with the Senior Regulatory Affairs Officer, Manufacturing sites, Corporate Regulatory Affairs, EURMEA Regulatory Affairs, Marketing and Medical Safety, the Regulatory Affairs Officer will prepare and submit high quality and timely regulatory applications to the MHRA/IMB. Following licence submission, the Regulatory Affairs Officer will be in regular contact with the MHRA/IMB, responding to questions and ensuring progress leading to a...

Regulatory Affairs Officer

Salary:
£33k - £34k pa + Full Benefits package
Location:
Camberley
Job Type:
Permanent
Date Posted:
28-May-2012 17:30Add to My Shortlist

As the global leader in the ophthalmic marketplace, we are proud to meet the eye care needs of millions of people worldwide. For over 60 years, we have developed, produced and marketed the most advanced products available in ophthalmology. Dedicated to the provision of not only the highest quality eye care products, but to also making significant contributions towards the... We continue to grow from strength to strength and have recently been united with a leading eye care company to create a dedicated and focussed eye care business offering the widest spectrum of eye care products, serving the full life cycle of patient needs. In close collaboration with the Senior Regulatory Affairs Officer, Manufacturing sites, Corporate Regulatory Affairs, EURMEA Regulatory Affairs, Marketing and Medical Safety, the Regulatory Affairs Officer will prepare and submit high quality and timely regulatory applications to the MHRA/IMB. Following licence submission, the Regulatory Affairs Officer will be in regular contact with the MHRA/IMB, responding to questions and ensuring progress leading to a...

Senior Regulatory Officer

Salary:
£42k - £43k pa + Full Benefits package
Location:
Camberley
Job Type:
Permanent
Date Posted:
28-May-2012 16:53Add to My Shortlist

As the global leader in the ophthalmic marketplace, we are proud to meet the eye care needs of millions of people worldwide. For over 60 years, we have developed, produced and marketed the most advanced products available in ophthalmology. Dedicated to the provision of not only the highest quality eye care products, but to also making significant contributions towards the... grow from strength to strength and have recently been united with a leading eye care company to create a dedicated and focussed eye care business offering the widest spectrum of eye care products, serving the full life cycle of patient needs. We currently have an exciting opportunity for a Senior Regulatory Affairs Officer within the Regulatory Affairs Department UK & Ireland. This position will report to the Head of Regulatory Affairs, UK & Ireland. Degree qualified in a life science subject, the successful applicant will have solid experience and knowledge of the full range of regulatory disciplines within Pharma and ideally have experience of...

Regulatory Affairs Director

Salary:
Competitive Salary
Location:
Surrey
Job Type:
Permanent
Date Posted:
26-May-2012 00:00Add to My Shortlist

Primary Goal Responsible for directing all regulatory activities and developing and implementing strategies for timely approvals of Phase I through Phase IV clinical trial applications; counselling and overseeing regulatory teams; ensuring timely preparation and submission of regulatory documentation to European and international drug regulatory authorities; ensuring the quality, content and format of regulatory submissions; and interacting with regulatory agencies, project team members and development partners. Key Responsibilities & Critical Objectives Assist in the new product development of and manage the execution of the global regulatory strategy for all IND/non-IND/IDE/non-IDE-based products.Coordinate the preparation of regulatory submissions to international health authorities, including original CTAs, IMPDs, MAAs and Variation(s) submissions and CTA amendments. Assemble and evaluate CMC, non-clinical and clinical application documents to ensure completeness of applications. Manage critical projects and drive multiple, early-stage projects with a minimum of supervision.Coordinate with other departments to achieve project development goals. Represent the company...

Senior Regulatory Affairs Officer

Salary:
35000
Location:
Surrey
Job Type:
Permanent
Date Posted:
26-May-2012 00:00Add to My Shortlist

You will be working in close collaboration with Manufacturing sites, Corporate Regulatory Affairs, EURMEA Regulatory Affairs, Marketing Managers and Medical Safety, the Senior Regulatory Affairs Officer will prepare and submit high quality and timely regulatory applications to the MHRA/IMB, coordinate activities with Regulatory Affairs Officers and act as key UK/Ireland contact within regional regulatory organisation. Following licence submission, the Senior Regulatory Affairs Officer will be in regular...

Head Of Business Development

Salary:
£70,000 - £110,000
Location:
London, South East England, England, Home Based, West Sussex, Surrey
Job Type:
Permanent
Date Posted:
28-May-2012 12:50Add to My Shortlist

I am currently working with an international Regulatory consultancy who are looking for a Head Of Business Development. This company has gone from strength to strength without a business development department. Due to their success they are now looking for an experienced business developer to start this department and drive this consultancy forward. The ideal candidate will posess the following; 5 years plus business development in a cro or consultancy capacity. MUST have a background in regulatory affairs. MUST be able to work office based in the South East. For more information, please contact Stuart Gill on 01293 776 644. Barrington James is a professional recruitment consultancy who specialises in the placement of high calibre candidates within the Pharmaceutical Industry. With well over 30 years' experience within the...

Medical Affairs Manager (Acquired Bleeding)

Salary:
On Application
Location:
Surrey, London, East Sussex, Kent, Middlesex, West Sussex
Job Type:
Permanent
Date Posted:
26-May-2012 00:00Add to My Shortlist

Benefits: Standard (including car and bonus) JOB SUMMARY This is an exciting opportunity for an experienced Medical Information / Medical Scientific Affairs specialist looking to further their career within Medical affairs. You will be responsible for handling UK Medical Information queries, ZINC review and providing product specific and SOP training internally and externally as required. BACKGROUND Our client is a global leader in the Biotherapeutics industry. They research, develop, manufacture and...

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...

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]

Quality and Regulatory Manager

Salary:
On Application
Location:
Surrey, Staffordshire, Warwickshire, Worcestershire
Job Type:
Permanent
Date Posted:
25-May-2012 09:02Add to My Shortlist

JOB SUMMARY: The Quality Manager position is new to this company and therefore you will not only be bringing your expertise to the company, but you will be an influential member of the management team from the outset. BACKGROUND Initially this role will focus on the Quality side, however there is an aim for the individual to develop and gain... systems. With Head Offices based in Surrey and manufacturing in the West Midlands travel between the sites will be required. PRIMARY DUTIES *Lead on the Quality Management System across the multiple Company sites, UK and USA. *Liaison with The Notified Body, including preparation for surveillance visits for CE recertification and Health Canada inspections. *Corresponding with, and hosting FDA inspections visits as required. *Implementing and documentation of GMP as required by FDA purposes. *Identifying any discrepancies in the QMS, product or project compliance and addressing them through appropriate channels and support the implementation of corrective actions *Responsible for the implementation and monitoring...

Pharmacovigilance and Medical Review Manager

Salary:
On Application
Location:
Berkshire, Buckinghamshire, Surrey, London
Job Type:
Permanent
Date Posted:
25-May-2012 09:02Add to My Shortlist

JOB SUMMARY We are seeking to appoint a Pharmacovigilance and Medical Review Manager who will report directly to the Director of their local R&D structure. Covering the UK, the Pharmacovigilance and Medical Review Manager will assist in all aspects of local Medicinal Safety, in accordance with applicable regulatory requirements, guidelines, laws, and Servier quality standards and practices and in close... reference 5217 Only candidates with EU work authorisation will be considered. Keywords: Pharmacovigilance Manager, PV Manager, Drug Safety Physician, Medical review Manager, Global PV Manager, Buckinghamshire, Servier Laboratories 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]

Chartered Structural Engineer

Salary:
£38k - £55k pa + package
Location:
Camberley, Croydon, Guildford, Kingston Upon Thames, Richmond Upon Thames, Surrey
Job Type:
Permanent
Date Posted:
25-May-2012 09:07Add to My Shortlist

Senior Structural Engineer Surrey £38,000 to £52,000 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...

Chartered Structural Engineer

Salary:
£38k - £55k pa + package
Location:
Camberley, Croydon, Guildford, Kingston Upon Thames, Richmond Upon Thames, Surrey
Job Type:
Permanent
Date Posted:
25-May-2012 09:07Add to My Shortlist

Senior Structural Engineer Surrey £38,000 to £52,000 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...

Clinical Research Physician - Oncology, UK

Salary:
Excellent + Benefits
Location:
Berkshire, Buckinghamshire, Oxfordshire, Hampshire, London, Surrey, Uk
Job Type:
Any
Date Posted:
29-May-2012 00:00Add to My Shortlist

Clinical Research Physician - Oncology My client, a leading pharmaceutical organisation with an international presence are looking to recruit a pharmaceutical physician with a background in Oncology at either Associate Director or Director level. Role Detail: Working in a Uk-based role, but as part of a global team, you will be responsible for the management and development of PI - III clinical studies in Oncology. You will work in a matrix-management style environment and collaborate with various internal teams such as Clinical Operations, Regulatory Affairs, Medical Affairs and Pharmacovigilance. Your main duties will be as follows: - Medical & scientific input into clinical development strategy and implementation, for Phase I - III studies - Management and directorship of projects within the therapy area - Compilation of clinical development protocols, regulatory documents and clinical study reports...

Regulatory Affairs Manager, Emerging Markets

Salary:
£Negotiable + Benefits
Location:
Middlesex, Surrey, Hertfordshire, London, Essex, Berkshire, South East England
Job Type:
Any
Date Posted:
28-May-2012 15:46Add to My Shortlist

Regulatory Affairs Manager, Emerging Markets Location: Middlesex Employment type: Permanent Salary: Competitive An excellent opportunity to work as a Regulatory Affairs Manager, within Emerging Markets, has arisen with an expanding organisation in Middlesex. The successful Regulatory Affairs Manager will provide product development services that help biopharmaceutical and medical device companies obtain and maintain their products on the market. Responsibilities will involve: *Delivering world-class...

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