QC Analyst

This is a Shift Based Role | Full Time 40hrs Per Week | Monday to Sunday (5 Days Out of 7 Working on a Rotational Basis)

•  Morning Shift - 05:45am - 2:15pm
•  Afternoon Shift - 1:45pm - 10:15pm
• Evening Shift - 9:45pm - 06:15am

• Morning & Afternoon Shift Allowance £2,500.00 Per Annum 
• Night Shift Allowance £3,500.00 Per Annum

Our Client, Located Near to Wellingborough are Seeking an QC Analyst to join their Pharmaceutical Quality Control Laboratory Team, who are Responsible for Performing Analytical Testing, Conducting Investigations, and Ensuring Regulatory Compliance. 

ROLE

• Routine and Non-Routine Analysis, Using HPLC and Other Analytical Techniques
• Testing of Raw Materials, Finished Products, Stability Samples, and In-Process Samples
• Accurately Review and Interpret Analytical Results
• Ensure Laboratory Documentation is Completed in Compliance with GMP and Data Integrity Requirements
• Support OOS, OOT, Deviation, and CAPA Investigations
• Participate in Method Validation, Verification, and Transfer Activities
• Maintain Compliance with SOPs, GMP, ICH Guidelines, and CFR Requirements
• Assist with Laboratory Housekeeping, Calibration, and Equipment Maintenance
• Work Collaboratively with Other Site Departments

REQUIRED

• Degree in Chemistry or Pharmaceutical Sciences
• Minimum 3 to 4 Years’ Experience in a Pharmaceutical QC Laboratory
• Hands-on HPLC Experience
• Experience with a Variety of Analytical Techniques e.g. UV, FTIR, and Karl Fischer
• Sound Knowledge and Experience of GMP, Data Integrity, and Regulatory Compliance
• Experience with Chromeleon or Similar CDS Software
• Strong Analytical and Problem-Solving Skills
• Good Documentation Skills
• Ability to Work Independently and Manage Priorities Effectively
• Experience with Stability Studies and Method Validation
• Exposure to Investigations, Including OOS/OOT