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.
Requirements
Key Responsibilities & Accountabilities
* Carry out all work in accordance with written procedures, protocols, and processes.
* Inform the Shift Team Leader - QC of any non-conformities discovered and actively investigate root causes.
* Keep accurate, legible written records of work and follow GXP standards at all times.
Main Tasks
* Perform analysis of starting materials, intermediates, and finished products as per written procedures.
* Provide accurate records of work carried out.
* Adhere to GCLP, GMP, and safe working practices.
* Propose improvements to analytical methods or practices and participate in department and company projects.
* Perform calibration checks and calculation checks on analysis records.
* Carry out tasks as required to meet business and department needs.
* Meet daily and long-term schedules and performance objectives.
Relationships
Liaise with Operations, Global Technical, Pharmaceutical Development, and Regulatory Affairs departments on various issues.
Skills & Knowledge
Ideally qualified to degree level in chemistry or a life science. Candidates with lesser formal qualifications but substantial pharmaceutical analytical laboratory experience and troubleshooting skills may also be considered.
Our benefits vary by location; please contact the Norgine TA representative for more information.
Join Us
If this sounds good, learn more about your career with Norgine and apply now.
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