CK Group are recruiting for a QA Technical Support, to join a company in the pharmaceutical industry, at their site based in Worthing, on a contract basis for 12 months.
Salary: £15.64 per hour PAYE.
QA Technical Support Role: As part of the team, you will provide analytical technical support to QA and the site.
Key Responsibilities Include:
The analytical technical support for QA and the site. Investigation of issues with analytical methods and instrumentation. Analytical Support for plant trials and validation. Non-routine analysis. Preparation and presentation of reports.
Your Background: The candidate must have experience of working under cGxP. Experience in a pharmaceutical GMP environment such as QA, Development or R&D using chromatography, spectroscopy, electrochemical and/or physical testing techniques. Good planning, organizational and time management skills along with an ability to make decisions, solve problems, negotiate, influence and communicate effectively with others. Good interpersonal skills to facilitate effective interaction with Business Unit teams and Contractors. Knowledge of IT systems and well developed verbal, written numeric and presentation skills.
Company: Our client is one of the largest global healthcare companies researching, developing and supplying innovative medicines, vaccines and healthcare products with their global headquarters in the UK. They invest around £1bn in research and development in the UK annually.
Location: This role is based at our client's site in Worthing.
Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 112 301.
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. #J-18808-Ljbffr
Salary: £15.64 per hour PAYE.
QA Technical Support Role: As part of the team, you will provide analytical technical support to QA and the site.
Key Responsibilities Include:
The analytical technical support for QA and the site. Investigation of issues with analytical methods and instrumentation. Analytical Support for plant trials and validation. Non-routine analysis. Preparation and presentation of reports.
Your Background: The candidate must have experience of working under cGxP. Experience in a pharmaceutical GMP environment such as QA, Development or R&D using chromatography, spectroscopy, electrochemical and/or physical testing techniques. Good planning, organizational and time management skills along with an ability to make decisions, solve problems, negotiate, influence and communicate effectively with others. Good interpersonal skills to facilitate effective interaction with Business Unit teams and Contractors. Knowledge of IT systems and well developed verbal, written numeric and presentation skills.
Company: Our client is one of the largest global healthcare companies researching, developing and supplying innovative medicines, vaccines and healthcare products with their global headquarters in the UK. They invest around £1bn in research and development in the UK annually.
Location: This role is based at our client's site in Worthing.
Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 112 301.
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. #J-18808-Ljbffr
