- To support new equipment qualification, lab computerized system and new chemistry lab set up where required
- To perform transfer/verification/validation of laboratory procedures within the team where required
- To prepare technical documentation including but not limited to protocols, analytical write-ups, standard operating procedures, specifications, investigations and reports.
- To perform analysis of incoming goods, intermediates and/or finished products under cGMP conditions for QC release or as part of stability studies.
- To review analytical and laboratory data within the department for accuracy, completeness and compliance with detailed procedures.
- To perform planned preventative maintenance and performance calibrations on equipment.
- Management of QC chemical, reference standard and consumable stock levels
- To maintain own training records
- Participate/chip in Practical Process Improvement initiatives (PPI) or continuous improvement in the lab
- Support and encourage a Quality Culture and company 4i values throughout QC
- Ensure cGMP is applied in their area of work and align with cGMP in all areas of the business.
- To work with HSE, cGMP and 5S in mind at all times.
- Undertake ad-hoc activities that may be required by the business
- To support shift work (if necessary) in future
Keys to Success:
This is a fixed term (1 year) role.
Education
Degree in Chemistry or equivalent experience in a strongly related scientific field
Experience
- At least 3 years relevant industrial experience
- Ability to work independently and adhere to critical timelines
- Excellent attention to detail
- Excellent organisational skills
