Conduct testing according to written procedures, Raw material, in-process and finished product testing in the Analytical laboratory.
Collect, compile and analyse data and prepare laboratory reports.
Ensures all notebooks/logbooks/Worksheets are completed and reviewed in a timely manner.
Records all information and raw data only on designated forms or logbooks and/or via appropriate systems.
Assist manufacturing/operations/quality in solving quality-related problems.
Ensures Non-conformances, laboratory investigations and out of specification results are documented and reported to Laboratory Management.
Ensure equipment, standards and other materials are approved/released prior to use.
Performs cleaning, preventative maintenance, verification of instruments and equipment where required.
Ensure all training is completed as per Laboratory Training Program.
Adherence to data integrity on site at all times.
Perform and assist with additional duties as may be directed by the Supervisor.
Identify and implement opportunities for improvement.
Support Internal/External Audits.
Communicates any concerns about work process regarding environmental impact, health or safety issues to their Manager.
To build quality into all aspects of work by maintaining compliance to all quality requirements, including Good Manufacturing Practice, Good Laboratory Practice and Good Documentation Practice (GMP, GLP and GDP)
Be able to communicate clearly and to form strong working relationships with colleagues.
Work on own initiative and be capable of developing solutions to problems as part of a team.
Willing to operate in a flexible manner and be able to switch priorities at short notice.
Demonstrate problem solving in delivering process and analytical understanding.
Willingness to travel when required.
Requirements
Level 6 qualification in Chemistry or related discipline.
Ideally 1 years work experience within a GMP environment.