CANDIDATES
EMPLOYERS
TOOLBOX
Seltek Consultants Limited,
25a Hockerill Street,
Bishop's Stortford,
Hertfordshire,
CM232DH
UK
Tel: 01279 657716
Email: sales@seltekconsultants.co.uk

|
|
We handle many vacancies for experienced quality assurance managers. Below you'll find examples of some typical Jobs.
QUALITY ASSURANCE AUDITOR |
An excellent opportunity to gain auditing experience within the GCP environment! If you are an experienced GLP/GMP auditor or a CRA looking to move into the quality assurance field this is the role for you! Due to recent expansion in the quality operations group our client, a leading provider of drug development services, has an urgent need for auditors to conduct a variety of clinical audits across Europe including site, system, vendor, process and documentation audits. Training will be provided in GCP/auditing processes if required. A competitive remuneration package is available including pension, healthcare, life assurance, 23 days holiday, bonus scheme and flexible working arrangements. Call now to find out more!
Applications are invited from candidates with a good degree and either previous GCP/GLP/GMP auditing experience OR clinical monitoring/project management. Candidates with GLP/GMP only must have at least two years' auditing experience. |
| |
MANAGER,INTERNATIONAL QUALITY ASSURANCE |
A major CRO with offices throughout Europe and across the US is expanding its international QA department with the addition of an experienced senior manager. This company has expanded rapidly over the last three years through acquisition and now is an exciting time to join them! The main function of this role is the implementation and maintenance of a quality management programme including system qualification/validation and vendor qualification programmes. Reporting into the Chief Operating Officer in the UK you will work closely with the QA Director based in the US to establish a common QA function between the international and US operations. This role will evolve and grow as the department expands internationally leading to departmental/staff management responsibility. A rare and exciting opportunity to influence the development and direction of a growing function within an innovative company! An excellent benefits package is available including pension, car allowance, 25 days holiday and life assurance.
To be considered you must have at least five years' auditing experience to GLP/GCP requirements in both North America and Europe and two years' management experience. Clinical trial management experience is highly desirable. |
| |
GCP SPECIALIST |
| Develop your GCP auditing skills! An international drug development company conducting phase II-IV clinical trials in a range of therapy areas has an urgent requirement for an experienced auditor to join their expanding European QA department. This role is partly office based in the South West and will involve 50% travel within Europe to conduct a range of GCP audits: site, system, process, facility, vendor and documentation. Applications welcomed from experienced GMP/GLP auditors with a basic knowledge of GCP. |
|
|
LATEST CLINICAL JOBS
A varied and challenging Clinical Research Associate (CRA) role with a leading, specialist oncology research operation in the UK. This organisation is channeling vast amounts of funding into oncology research and in the last two years alone has been involved in the development of various novel cancer treatments.
With increased funding ... more
One of the top ten clinical research organisation (CRO) is expanding, and is keen to recruit a Senior CRA to join their team in the Netherlands. The role can be office or field based with regular travel to monitoring sites. You will assist in managing large scale clinical trial projects or act as a project manager for small scale projects ensuring on time and on budget performance ... more
This leading CRO is looking to recruit a Project Manager to manage phase IV clinical research projects throughout Europe.
This position has arisen due to expansion, as they have recently won a large number of phase IV proposals.
You will lead the clinical team to ensure on-time, on-budget performance, review and approve regulatory and administrative documents from investigator sites, as well as reviewing CRF’s and SAE reports.
You will also ... more
One of the top ten clinical research organisation (CRO) is expanding, and is keen to recruit a Senior CRA to join their team in Germany...more
|