Quality Lab Analyst
Posted 15 hours 2 minutes ago by New Scientist
Permanent
Not Specified
Laboratory Jobs
Angus, Montrose, United Kingdom, DD100
Job Description
CK Group are recruiting for a QC Lab Analyst, to join one of the top ten companies in the pharmaceutical industry, on a contract basis for 12 months.
Salary:
PAYE £20.97 per hour (inside IR35).
Quality Lab Analyst Role:
Your Background:
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 clients site in Montrose, Scotland.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference .
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Salary:
PAYE £20.97 per hour (inside IR35).
Quality Lab Analyst Role:
- To work as part of a high-performing team and is responsible for carrying out routine analysis on IPC, raw materials, manufactured and stability samples using classical and chromatographic techniques as appropriate. This includes the use of M-ERP and other IT systems to manage and report data.
- To provide an effective analytical service for the analysis of non-routine samples and to assist in the troubleshooting of production problems.
- Tasks are carried out with integrity, a positive attitude and a willingness to work across boundaries to optimize efficiencies and reduce waste.
- To be actively involved in activities that are required for the effective running of the quality laboratory.
- Activities include, but are not limited to the review and preparation of procedures e.g. LSOP s, validation reviews, COSHH and risk assessments and Glaxo Production System (GPS) improvement activities.
- To work to current Good Laboratory Practice (cGLP) in a highly-regulated environment, following the defined procedures (LSOP s, GSOP s and other applicable documentation).
Your Background:
- Previous work experience in a Quality Control lab.
- Competency in a range of analytical techniques e.g. chromatography and classical tests.
- Experience in quality/compliance in a GMP environment.
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 clients site in Montrose, Scotland.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference .
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.