Quality Management Director - United Kingdom - Intertek Group Plc

Description

Due to growth, we have an exciting opportunity to grow our Bioanalytical Team with a new Study Director.

you will demonstrate good interpersonal skills with the ability to network and build close relationships in order to collaborate with both Clients and members of the business in order to ensure that the business TQA promise is consistently met.

Coming from a scientific background to Degree level and knowledge within a defined area(s) with good project management skills.

Project management of GLP and GCP clinical studies

Good interpersonal skills with the ability to network and build close relationships in order to collaborate with both Clients and members of the business in order to ensure that the business TQA promise is consistently met.

Scientific background to 1st Degree level and knowledge within a defined area(s) with good project management skills.
Good experience of preparing documents with technical support or guidance across multiple projects.
Good working knowledge of the Chemical and Pharmaceutical Industry with good commercial understanding and natural business acumen.

You will demonstrate your skillset within a technical area as well as project management skills and have the confidence to provide information and background on specific programmes of work to both Colleagues and Clients.

You will be accountable for being the Project Manager for both existing and developing Clients and you will have good communications skills and the ability to converse with key contacts, providing them with accurate information and progress reports on a consistent basis.

Overall responsibility for the scientific, administrative and regulatory conduct of GLP and GCP studies in a GxP regulated laboratory
Overseeing Pharmacokinetic, Immunogenicity and Biomarker validation studies in accordance with regulatory guidance.
Preserving data integrity ensuring all data are accurately and fully documented following ALCOA plus principles and computerised systems are validated and fit for use in the study
Ability to produce high quality reports, as a complete, true and accurate record of study conduct and conclusions
Skilled project management, including ability to generate / edit multi-technique reports.
Able to define projects customer requirements, manage and deliver multi-technique projects.

Ability to manage and report projects, drawing on findings from several techniques with technical support to solve customer problems.

Join Intertek and become part of our global network of inspiring and entrepreneurial colleagues. We are a global family that values diversity and we thrive working together with precision, pace and passion.

We are working to make the world Ever Better, ensuring the quality, safety and sustainability of products and services used by millions of people around the world.

Competitive salary/benefits
Development and career opportunities around the Globe
In this opportunity you'll be joining our Bioanalytical Immunoassay team, based at Intertek Pharmaceutical Services Manchester (IPSM), Blackley Manchester