QC Analyst Level 3
Norgine, United Kingdom
Job Description
Working 38 hours per week on a two shift rotation and working one weekend in four you will be required to:
MAIN PURPOSE:
To carry out and record the analysis of materials according to written procedures.
KEY RESPONSIBILITIES amp; ACCOUNTABILITIES:
The job holder is responsible for carrying out all work in accordance with written procedures.
The job holder is responsible for informing the Shift Team Leader - QC of any non-conformities discovered and for actively investigating any non-conformities with a view to establishing root cause.
He/she is responsible for keeping accurate, legible written records of their work and following GXP’s at all times.
MAIN TASKS:
- Perform the analysis of starting materials, intermediates and finished products in accordance with written procedures.
- Provide accurate records of work carried out.
- Perform all duties in accordance with GCLP (Good Control Laboratory Practice), GMP (Good manufacturing Practice) and safe working practices.
- Propose improvements to analytical methods or working practices and participate in department and company improvement projects.
- Perform calibration checks in accordance with written procedures.
- Perform calculation checks on analysis records.
- To carry out tasks as required to suit business needs and department needs and as appropriate to the job role.
- Meet day to day and longer term schedules and performance objectives.
RELATIONSHIPS:
Required to liaise with Operations, Global Technical, Pharmaceutical Development and Regulatory Affairs Departments on a variety of issues and information exchanges.
SKILLS amp; KNOWLEDGE:
Ideally qualified to degree level in chemistry or a life science. Lesser formal qualifications may be acceptable when coupled with substantial pharmaceutical analytical laboratory experience and experience in analytical trouble shooting.