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GLP LC-MS Study Director

North YorkshirePermanent
Experience Dependant
Job Reference: J5632153
Updated On: 04/09/2019
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Contract Research Organisation, Contract Testing Organisation, Life Sciences

Skills: Chemistry - Analytical - HPLC (Method Devlopment), Chemistry - Analytical - LCMS, Chemistry - Analytical - Method Validation Only, Chemistry - Analytical - Method Development Only, Chemistry - Analytical - UPLC

Job Information

Role Overview

Are you an experienced GLP Study Director looking for a new exciting opportunity?

We are currently looking for a GLP Study Director to join a leading contract testing company based in the North Yorkshire area.

As the GLP Study Director you will be expected to help the company directors implement and manage the principles of GLP, GCP and health and safety compliance within the company and advise other bioanalysts and the Laboratory Head in maintaining an efficient, safe, GLP and GCP compliant laboratory.

Key Duties and Responsibilities

Your duties as the GLP Study Director will be varied however the key duties and responsibilities are as follows:

1. As the Study Director, you will be all of the study data (validation, analytical and equipment studies) as well as supervise staff performing the laboratory work, draft study and validation protocols, review all study data for accuracy and GLP / GCP compliance as well as transfer study data into reports.

2. As well as study directing, you will be involved in personnel training and development for performing quantitative analysis using LC-MS and multiplexed immunoassay whilst providing assistance in the technical, scientific, practical and GLP and GCP compliance of all work in the company.

3. Additionally, alongside the study directing responsibilities, you will have to prepare proposals for major capital investment for authorisation by the Directors, represent the company at internal and external meetings as well as perform QC procedures for studies performed by other Study Directors or analysts.

4. Lastly, you may be required to help with recruitment, staff selection, performance assessment, training and development as well as setting and assessing staff performance standards and objectives.

Role Requirements

To be successful in your application to this exciting opportunity as the GLP Study Director we are looking to identify the following on your profile and past history:

1. Relevant Life Sciences degree and experience using LC-MS for analysis in a GLP regulated CRO laboratory is essential.

2. Proven industry experience in study directing, managing projects or writing reports would be beneficial, however, not essential, as this role is also open to those looking to step into a Study Directing position.

3. You will need to have had hands on experience working in a regulated environment, following SOPs, protocols and ensuring Health and Safety regulations within a laboratory.

Key Words: GLP Study Director | Study Manager | LC-MS | Chemistry | Contract Testing Laboratory | Analyst | Clinical Testing
Debra Fong
Your Recruitment ConsultantDebra Fongdebra.fong@hyperec.com
DisclaimerHyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.