Role & Responsibilities • Ensure day to day and routine analysis is completed in an effective and timely manner • Interface with other parts of the Quality Directorate to ensure that there is a smooth and efficient flow of products from the site • Support interfaces with other departments to ensure they are effective for all parties • Ensure quality or compliance issues are escalated through the appropriate management lines and processes • Responsible for carrying out routine analysis on IPC, raw materials, manufactured and stability sample using classical and chromatographic techniques as appropriate • Assist in the troubleshooting of production problems • Review and preparation of procedures (eg LSOPs, validation reviews, OE improvements) • Work to GLP in a highly regulated environment • Required to be actively involved in various audit teams (eg GMP) Experience & Requirements • Education to degree (or equivalent) level in a relevant area (biochemistry, pharmaceutical sciences, chemistry, etc) • Understanding of GMP and GLP • Experience of using HPLC • Industry experience is advantageous but not a necessity If you have any questions or are interested in this role please contact Owain at CY Partners">

Quality Lab Analyst

Quality Lab Analyst

Location Scotland

Salary £28,000 - £31,000

Contract Temporary

Reference QLA001OW

Date Posted

Consultant

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Less than an hour left to apply


A world leading pharmaceutical company is looking to hire a quality lab analyst on an initial nine-month temporary contract, with the possibility of extension. The role would be based out of Montrose and a competitive salary.

Role & Responsibilities
• Ensure day to day and routine analysis is completed in an effective and timely manner
• Interface with other parts of the Quality Directorate to ensure that there is a smooth and efficient flow of products from the site
• Support interfaces with other departments to ensure they are effective for all parties
• Ensure quality or compliance issues are escalated through the appropriate management lines and processes
• Responsible for carrying out routine analysis on IPC, raw materials, manufactured and stability sample using classical and chromatographic techniques as appropriate
• Assist in the troubleshooting of production problems
• Review and preparation of procedures (eg LSOPs, validation reviews, OE improvements)
• Work to GLP in a highly regulated environment
• Required to be actively involved in various audit teams (eg GMP)

Experience & Requirements
• Education to degree (or equivalent) level in a relevant area (biochemistry, pharmaceutical sciences, chemistry, etc)
• Understanding of GMP and GLP
• Experience of using HPLC
• Industry experience is advantageous but not a necessity

If you have any questions or are interested in this role please contact Owain at CY Partners

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Quality Lab Analyst

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