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QC Analyst - Dundee

CK Group- Science, Clinical and Technical
Posted 5 days ago, valid for 20 days
Location

Dundee, City of Dundee DD1 1XA, Scotland

Salary

£24,000 - £28,800 per annum

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Contract type

Full Time

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Sonic Summary

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  • CK Group is seeking a QC Analyst for a 6-month contract at a leading pharmaceutical organization in Dundee, focusing on veterinary products.
  • The role requires a degree in a relevant scientific discipline and experience as an analytical chemist, particularly with HPLC and GC techniques.
  • Key responsibilities include ensuring compliance with health and safety practices, conducting various laboratory tests, and supporting team leads with technical expertise.
  • Applicants should have strong knowledge of GMP, data integrity, and troubleshooting skills, along with experience in a pharmaceutical or laboratory environment.
  • The position offers a salary of £25,000 per annum and requires candidates to have the right to work in the UK.
CK Group are recruiting for a QC Analyst, to work within a Quality Control Laboratory, for a leading pharmaceutical organisation that develop and manufacture veterinary products.


The QC Analyst will be working on site in Dundee, on a contract basis for 6 months.


Key Responsibilities:
  • Follow Health and Safety practices and policies by reporting all incidents, identifying risks and/or hazards, wearing of PPE and guiding others on HS&E.
  • Ensure quality and compliance by practising good housekeeping, GLP, GMP and meeting Data Integrity requirements and guiding other to achieve this.
  • Perform testing as trained to support the department deliverables as required:
    • Starting materials, finished products and stability samples.
    • Non-routine and project testing/work.
    • Laboratory investigations for OOT/OOE/OOS.
    • Validation testing activities.
  • Support team leads by providing technical expertise and support to analysts.
  • Raise and investigate OOS/OOT/OOE.
  • Support closure of team actions relating to CAPA/LIR/ change control/audit actions and method updates.

Your Background:

  • Educated to degree level or equivalent in a relevant scientific discipline such as Chemistry or Biology.
  • Experienced analytical chemist with experience in chromatographic (HPLC and or GC), spectroscopic and classical techniques.
  • Strong knowledge of GMP and Data integrity requirements in QC environments.
  • Strong troubleshooting skills.
  • Industry background in a Pharmaceutical, Laboratory or related environment.
  • Ability to conduct Laboratory investigations.
  • Ability to review documents and testing reports.
  • Experienced in Chromeleon Software.

Apply:


It is essential all applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.

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