Responsibilities:
- To support new equipment qualification, lab computerized system and chemistry lab set up
- 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 (including HPLC and GC) 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 documented 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
- To communicate optimally with others on site
- Participate/contribute 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
EH&S:
- Understand emergency procedures and align with safe systems of work.
- Ensure compliance with environment, health and safety and security policies and procedures, rules, signage and instructions at all times
- Ensure prompt reporting and investigation of all accidents, near misses and breaches of rules
Minimum Requirements/Qualifications:
- Degree in Chemistry or strongly related scientific field
- At least 2 years relevant industrial experience
- Ability to apply GMP regulations and other international guidelines to all aspects of the position.
- Ability to work independently and adhere to critical timelines
- Excellent attention to detail
