QC Analyst

QC Analyst

Our Client, A Pharmaceutical Manufacturing company, is currently seeking a QC Analyst to be part of a dynamic team within the QC function. They are looking for individuals who will support and drive the company’s vision to be the most valued global provider of high quality, competitively priced pharmaceutical products and to provide excellent services and support to customers.

RESPONSIBILITIES:

·        Displays the capability to learn and understand methods showing competency in the following technical areas: HPLC, IR, UV, dissolution & physical testing.

·        Maintain and follow all relevant Standard Operating Procedures (SOP’s).

·        Adherence to the existing methods with reference to pharmacopoeia’s, specifications, regulations and industry standards.

·        Full analysis of raw materials in a timely manner using appropriate analytical techniques with limited analyst related OOS.

·        Full analysis of finished product (tablets, boluses, veterinary drenches etc) in a timely manner using appropriate analytical techniques with limited analyst related OOS.

·        Full analysis of contract manufactured products in accordance with customer specifications with limited analyst related OOS.

·        Incoming inspection of foils, labels, bulk finished goods and injectable.

·        Calibration and maintenance of laboratory equipment as per calibration procedures.

·        Support the laboratory testing schedule to achieve an efficient QC system & Customer Service level of >95%.

·        To maintain all laboratory logbooks, notebooks & associated documentation to GLP.

·        Liaise with team leader/supervisor & production so that timely reporting of results is achieved.

·        Ensure timely feedback of all queries as appropriate.

·        Display ability and follow up on Corrective Actions.

·        Sending out samples for external analysis when requested.

·        Participating in internal/External Audits.

·        Liaising with external suppliers/vendors in relation to QC consumables.

·        Ensure existing quality procedures are followed and where appropriate suggestions/change control forms are prepared so that the quality system will be continuously improved.

·        To adhere to any agreed internal laboratory rota tasks.

·        To maintain good housekeeping and hygiene within the laboratory.

·        Adherence to laboratory safety measures at all times highlighting areas for improvement

·        Takes direction and asks questions

·        Develops own technical skills.

·        Takes a methodical, systematic and structured approach to organising work.

·        Ability to prioritise decision making differentiating between urgent and non-urgent.

·        Escalates issues appropriately.

·        Offers to help others when needed and creates a sense of harmony in the team.

·        Displays flexibility and shows willingness to learn and do that little bit extra.

REQUIREMENTS:

·        3rd level qualification – bachelor’s degree in a chemistry-based discipline.

·        2-5 years’ experience in a QC Analyst role.

·        Strong computer skills in MS Office.

·        Experience working within a pharmaceutical cGLP Environment.

·        Knowledge of EU GMP and US FDA Guidelines

·        Maintains the highest standards of ethical behaviour. Escalates issues appropriately.

·        Flexible and shows willingness to learn to develop technical skills.

If interested, please forward your most updated CV to [email protected]

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