QC Analyst II

This role is responsible for the performing routine laboratory procedures, transfer/verification/validation of methodology, and project work within the department to support manufacture and release of pharmaceutical products.  

Responsibilities: 

• To perform quality control analytical testing of incoming goods, intermediates and/or finished products under cGMP conditions for QC release or as part of stability studies. 

• To prepare 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 transfer/verification/validation of laboratory procedures within the team where required. 

• To assist with technical troubleshooting related to analytical equipment, analytical methods or unexpected results 

• 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. 

EH&S: 

• Understand emergency procedures and comply 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