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Norgine

QC Analyst Level 3

Posted 15 Hours Ago
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Hengoed, Caerphilly, Wales
Entry level
Hengoed, Caerphilly, Wales
Entry level
As a QC Analyst Level 3, you will analyze materials per written procedures, ensure compliance with GXP, GMP standards, investigate non-conformities, and maintain accurate records. You will collaborate with various departments to improve analytical methods and ensure safety in operations.
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Description

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.

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.

Requirements

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

RELATIONSHIPS:

Required to liaise with Operations, Global Technical, Pharmaceutical Development and Regulatory Affairs Departments on a variety of issues and information exchanges

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.

Benefits

Our benefits may vary per location. Please liaise with the Norgine TA representative to obtain more information.

Sound good? Find out more about the career you’ll have with Norgine, then apply here.


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Top Skills

Chemistry
Life Sciences

Norgine Uxbridge, England Office

Widewater Place, Uxbridge, United Kingdom, UB9 6NS

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