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
* IT literate (Minimum Microsoft Office Suite)
REMUNERATION
* £28k - £32k p/a + Benefits
Salary description
£28000.00 - £32000.00 per year