Want a 3D Career? Join Norgine.
At Norgine, our colleagues Dare themselves to be different and try new things, Drive to achieve their goals and beyond, and Develop themselves and their community.
We call it the 3D career at Norgine and it offers you a fully-rounded experience with no limits.
Bring everything about yourself that you’re proud of, whether that’s your passion for making a difference, focus on others’ well-being, or intellectual curiosity to unleash in a fast-paced environment and supportive community.
In return, get a sense of belonging, a long-term career with ongoing development and upskilling, and a company that cares about people’s wellness as much as you do.
Because at Norgine, we transform lives with innovative healthcare solutions.
We have an exciting opportunity for a QC Analyst Level 3 to join Norgine.
The person holding this position will report to the QC Team Leader.

SKILLS & 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.

MAIN PURPOSE:

To carry out and record the analysis of materials according to written procedures.
If you want a multi-dimensional 3D career in a leading healthcare organisation, join us.

KEY RESPONSIBILITIES & ACCOUNTABILITIES:

• The job holder is responsible for carrying out all work in accordance with written procedures, protocols and processes
• 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