An Excellent Career Opportunity for an Experienced Quality Control Analyst, Supporting the QC Supervisor and QC Lead Analyst
ROLE
Perform Routine Analytical Testing on Incoming Materials and Finished Products
Ensuring All Analytical Standards, Methods, Sampling Processes, and Training Requirements are Executed in Full Compliance with SOP s
Coordinate with QC Lead Analyst and Other Team Members to Ensure All Analytical Work Assigned is Achievable and Delivered in a Timely Manner
Peer-Review or Bench-Check QC Test Documentation and Results for the QC Analytical Team
Report Any Issue with Availability and Validity of Protocols, Reports, Specifications, or Retest Date for Calibration, Qualification and Validation of Equipment
Report on Any Issue with the Purchase, Replacement and Availability, or Delivery, of the Required Reference Standards, Chemicals, Reagents, etc
Consistently Follow the Data Integrity and Governance Requirements in SOP s
Demonstrate Capabilities on HPLC, KF Titration, Dissolution Testing and Physical Testing of Dosage Forms and Packaging
Prepare and Check Analytical QC Data before Presenting Results for Review
Completing allocated training and making sure that the training is effective by implementing QC analytical work assigned correctly.
Perform Routine or Special Assigned Duties to Check/Verify/Draft SOP s and Specifications Required to Meet Regulatory and Customer Requirements
REQUIRED
Certificate, Diploma or BSc in Chemistry, Medical Laboratory Science, Analytical Sciences, or Equivalent Science Degree with Strong Practical and Analytical Component
Substantial Analytical Experience in a UK Pharmaceutical QC Laboratory
Experience of a Wide Range of Laboratory Instrumentation and Analytical Techniques
Experience with HPLC Analysis and Analytical Method Troubleshooting, Ideally with Agilent Systems and OpenLab Software
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