Bioanalytical | CK Science

Posts Tagged ‘bioanalytical’

Study Director (Bioanalysis) – Yorkshire, UK

Thursday, July 22nd, 2010

Our client is currently seeking to recruit a Study Director to work within their Bioanalytical department at their site in Yorkshire on a permanent basis.

As a Study Director you will oversee bioanalytical studies, ensure that the studies are carried out to the required standards and approve the study data. You will be the single point of study control and have overall responsibility for the scientific, technical and regulatory compliance of studies allocated to you, as well as for the interpretation, documentation and reporting of results.

As an experienced Study Director you will be familiar with conducting all work in compliance with applicable regulatory requirements governing the work in which they are involved, such as GLP and GCP.

The ideal candidate for this Study Director role will be educated to degree level, or equivalent, or above in a related discipline, with experience in small molecule bioanalysis by LC-MS/MS and will also ideally be working in, or have experience within, Contract Research or a related industry.

Apply now

For more information, or to apply for this Study Director role, please contact PhilIppa Robertson on 0114 283 9956 pr email probertson@ckscience.co.uk. Please quote reference SH20087 in all correspondences.

Alternatively, click here to apply for this Study Director job now.

Tags: bioanalysis, bioanalytical, contract research organization, laboratory jobs, LCMS, research jobs, science jobs, study director, uk, yorkshire
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QA Manager (GCP) – London, UK

Tuesday, June 8th, 2010

A QA Manager is required to join a CRO based in London, UK.

As QA Manager, the main aim of your role will be to implement and manage the CRO’s Quality System and to develop and implement QA GCP audit strategy in line with the overall QA strategy. You will also be responsible for ensuring the compliance of their clinical trials in accordance with business and statutory regulations and reporting critical GCP non-compliance.

Working as a QA Manager, your main responsibilities will include:

Acting as the source of advice and guidance on GCP and SOP related quality issues and will determine the effectiveness of the Company’s quality systems and procedures.
Delivering the SOP Management System.
Assessing GCP non-conformities and non-compliant findings.
Supporting the implementation of technical training within the Company.
Co-ordinating with the GCP regulatory inspectorate client auditors and customers.
Ensuring compliance of the quality documentation related to Clinical processes and studies through audit and review.

The ideal candidate for this QA Manager position will be degree qualified (or equivalent) and will ideally hold a qualification in Quality or QA. This QA Manager job also demands a candidate with experience and knowledge in the following:

Industrial experience within QA.
Proven auditing experience across full range of clinical audit types including CROs, investigator sites, protocol, clinical study reports, systems and submissions.
Proven management experience.
A good knowledge of phase I – IV studies, bioanalytical, PK, skin, blood and urine laboratory analysis an experience auditing.

Apply Now

For more information, or to apply for this QA Manager job, please contact Jason Johal on 01438 723 500 or email jjohal@ckscience.co.uk. Please quote reference ST19921 in all correspondence.

Alternatively, click here to apply for this QA Manager job online now.

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If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.

Tags: audit, auditing, bioanalytical, central london, clinical audit, clinical study reports, cro, GCP, London, QA, QA Manager, quality assurance, SOP, south east, uk
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Senior Assay Scientist based in Liverpool, UK

Thursday, April 8th, 2010

Senior Assay Scientist based in Liverpool, UK

Our client is currently seeking to recruit an Assay Scientist to work with them on a permanent basis at their site in Liverpool.

As Senior Assay Scientist, you will be involved developing and maintaining an extensive portfolio of bioanalytical assays across a range of therapeutic areas for the pharmaceutical, biotechnology and healthcare sectors.

Reporting to the Laboratory Director, working as Senior Assay Scientist your main responsibilities will include:

Providing professional, scientific and technical support to laboratory team.
Liaising with the Laboratory Director, lead on identifying and developing new assays, products and services.
Preparation of research and scientific documentation in support of assay development, system and service validations and process changes.
Providing specialist and scientific knowledge and expertise to the clinical trials team in developing the company’s clinical trial capabilities and performance.
Liaising with Laboratory Manager to ensure the effective management and delivery of clinical trials within the laboratory to specified commercial and contractual specifications.
Ensuring effective management and operation of laboratory instrumentation, sample processing and reporting and all other general laboratory activities.
Liaising with Quality Manager, ensure all laboratory staff and systems operate effectively within the Quality Management System.
Liaising with the Data Manager, ensure the effective management, analysis, control and security of all data generated by or received by the laboratory.
Contributing to the wider scientific and commercial development of the company through the Group Scientific Committee and specified project work.

The ideal candidate for this Senior Assay Scientist role will be educated to degree level or equivalent, or higher in a Pharmaceutical or Biomedical subject and have postgraduate bioanalytical and scientific laboratory experience. A strong track record in developing new bioanalytical assays (LCMS) from first principles to implementation is also required. Entitlement to work in the EEA is essential.

How to apply:

For more information, or to apply for this Senior Assay Scientist role, please contact Philippa Robertson on 0114 2839956 or email probertson@ckscience.co.uk. Please quote refernce SH19195 in all correspondence.

About CK Science

CK Science is the largest independent scientific recruitment company in the UK. Our team of specialist recruiters are here to help you achieve your career ambitions within the scientific industry. We actively offer you careers advice, help with writing your CV, assistance with interview preparation and up-to-date information about the industry. We pride ourselves on providing an honest, straight-forward and trustworthy service to both our clients and candidates.

Tags: assay development, bioanalytical, Biotechnology, diagnostics, Jobs, jobs in science, laboratory jobs, LCMS, Liverpool, Merseyside, North West, Pharmaceutical, science jobs, science recruitment, scientific recruitment, scientist jobs, scientist recruitment, uk
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Senior Assay Scientist based in Liverpool, UK

Thursday, February 4th, 2010

Our client is involved in supporting healthcare providers and the pharmaceutical and biotechnology industries with technically advanced testing services. This innovative and dynamic company are currently looking for an Assay Scientist to work with them on a permanent basis at their site in Liverpool.

Reporting to the Laboratory Director, this Senior Assay Scientist job will involve developing and maintaining an extensive portfolio of bio-analytical assays across a range of therapeutic areas for the pharmaceutical, biotechnology and healthcare sectors.

Further responsibilities of this Scientist role will include:

Providing professional, scientific and technical support to laboratory team.
Acting as the primary lead in developing an extensive portfolio of bioanalytical assays, mainly in small molecules, across a range of therapeutic areas for the pharmaceutical and biotechnology sectors for clinical trials and routine service testing to the healthcare sector.
Preparation of research and scientific documentation in support of assay development, system and service validations and process changes.
Providing specialist and scientific knowledge and expertise to the clinical trials team in developing the company’s clinical trial capabilities and performance.
Liaising with Laboratory Manager to ensure the effective management and delivery of clinical trials within the laboratory to specified commercial and contractual specifications.
Liaising with Quality Manager, ensure all laboratory staff and systems operate effectively within the Quality Management System.
Liaising with the Data Manager, ensure the effective management, analysis, control and security of all data generated by or received by the laboratory.

The ideal candidate for this Senior Assay Scientist role will be educated to MSc, or equivalent, in the pharmaceutical, biomedical or life science sectors. Postgraduate bioanalytical and scientific laboratory experience is also desirable, preferably gained within a pharmaceutical, diagnostics or public sector laboratory environment. In addition, a strong track record of achievement in the development of new bioanalytical assays from first principles to implementation within a clinical trial or routine healthcare testing environment is also desirable.

If you would like to hear more about this Senior Assay Scientist job, please contact Philippa Robertson on 0114 2839956 or email. Please quote reference SH19195 in all correspondence.

Apply for this Senior Assay Scientist job now.

About CK Science

CK Science is the largest independent scientific recruitment company in the UK. Our team ofspecialist recruiters are here to help you achieve your career ambitions within the scientific industry. We actively offer you careers advice, help with writing your CV, assistance with interview preparation and up-to-date information about the industry. We pride ourselves on providing an honest, straight-forward and trustworthy service to both our clients and candidates.