About this role
Work Schedule
Environmental Conditions
Job Description
Position Summary:
This role is responsible for the performing routine laboratory procedures and pharmaceutical analysis in support for the QC Chemistry Team.
Responsibilities:
• To perform quality control analytical testing of incoming goods, intermediates and/or finished products under cGMP conditions.
• To manage consumable, reagent and chemical reference standard stock control within the department.
• To perform routine equipment checks of laboratory equipment (balances, pH meters etc)
• To prepare, complete and archive technical documentation including but not limited to analytical write-ups, standard operating procedures, specifications, investigations and reports.
• To perform planned preventative maintenance and performance calibrations on equipment.
• To perform washing of laboratory glassware
• To coordinate laboratory waste disposal streams
• To prepare laboratory bench reagents and solutions to be used in analysis
• To maintain own training records and support and train other team members as required.
• To participate in continuous improvement activities and look for further opportunities to progress the team/department.
• To communicate effectively with others on site and internationally, and to participate with them in problem solving activities.
• Ensure cGMP is applied in their area of work and comply with cGMP in all areas of the business.
• To work with HSE, cGMP and 5S in mind at all times.
• To carry out any other tasks which may be required from time to time.
Minimum Requirements/Qualifications:
• Working towards a degree in Chemistry or strongly related scientific discipline
• Theoretical and practical experience of analytical techniques and laboratory equipment
• Effective communication skills at all internal and external levels.
• Excellent attention to detail.
• Excellent organisational skills
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