QC Analyst x

Position: QC Analyst x 2 (Permanent)
My client, a Pharmaceutical company in Essex is looking for 2 QC analysts to join theire already established team. The QC Laboratory Analysts are responsible for conducting Quality Control testing and documenting laboratory testing in accordance with the MHRA and EU GMP Guidelines.

You will also be responsible for performing and assisting in the OOS investigations where required.

KEY RESPONSIBILITIES:

* Involvement in the control of Standard Operating Procedures.

* Planning testing workload under the supervision.

* Performing laboratory tests to produce reliable and precise data / results.

* Complying with the Company Standard Operating Procedures (SOP’s)

* Complying with GMP and carrying out routine tasks accurately and following strict methodologies to carry out analyses.

* Complying with company Health & Safety Policy and Procedures.

* To carry out any ad hoc duties as required.

* Ensuring laboratory test record data is recorded and stored in real time and in compliance to data integrity.

* Preparing samples, standards and reagents according to the relevant procedures.

* Maintain all areas other associated with laboratory in a presentable condition ready to being audited at any time.

* Performing method validations / method transfers where needed.

* Maintaining and operating standard laboratory equipment, for example titrators, pH meters etc.

* Assisting the Quality Team as directed.

* Assisting senior management in writing of validation protocols and linked reports.

* Ensuring the laboratory is well-stocked for performing the tests.

* Participating in self-inspections and regulatory inspections.

For a full JD and immediate consideration, please reach out ASAP