CK Group are recruiting for an exciting opportunity for a Senior QC Analyst to join a well established GMP Pharmaceutical manufacturer, at their site in Norfolk on a permanent basis.

The Company:
The company are continuously expanding and manufacture a variety of pharmaceutical products, medical devices and cosmetics.


Location:
This role is located close to the beautiful Norfolk coast.

Role Description:

• Carry out routine and non–routine testing activities of raw materials, bulk & finished packed samples in compliance with authorised test procedures using HPLC, GC & wet chemistry techniques.
• Ensure samples and test activities are scheduled to meet production requirements in line with the production plan and outstanding orders.
• Perform Environmental sampling and general Laboratory maintenance including equipment & calibration of apparatus.
• Providing training and support to other analysts in the team.
• Completion of investigations including LIs / OOS / OOT.

Your Background:

• Educated to degree level or above in life Sciences or a related field with relevant experience of working in a QC laboratory in a GMP environment.
• Experience of HPLC, GC, autotitrators, rheometric analysis, spectrometry and wet chemistry techniques.
• Experience of microbiological monitoring, COSHH assessment and computerised laboratory management systems would be desirable.
• Excellent interpersonal skills to be able to liaise effectively at all levels of the business.
• Competence in delivering training to a variety of internal audiences.
• Ability to plan, organise and prioritise tasks to achieve deadlines.

Apply:

It is essential that applicants hold entitlement to work in the UK. Please quote job reference 105620 in all correspondence.