Preproduction Quality Assurance Coordinator Opportunity - Scotland
Opportunity:
An exciting opportunity has been created due to company growth. My client a global pharmaceutical manufacturing company are looking to recruit a Preproduction Quality Assurance Coordinator based in Scotland where you will be responsible for ensuring the integrity of clinical trial supplies packaged at the site.
Day to day duties include:
- Generating clinical trial packaging documentation to meet the company, Client, Study and Regulatory requirements.
- Completing documentation in accordance to relevant SOPs and to comply with GMP.
- Maintaining high quality standards ensuring all deviations are documented as required.
- Competently performing tasks as detailed by the Preproduction skills matrix.
- Participating in the implementation of any new systems or upgrades to systems pertaining to Preproduction department.
- Participating in any process improvement initiatives to support Preproduction department.
- Keeping up to date with industry best practice.
The hours of work are Monday to Friday 8.00 am to 5.00 pm.
This is a 12 months contract based in Scotland which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance. The PAYE rate £13.33 per hour.
Skills:
To apply for the role of Preproduction Quality Assurance Coordinator you will have the following:
- Pharmaceutical or related scientific industry experience or education highly advantageous.
- Experience in GMP or GDP highly advantageous.
- Good IT skills.
- Attention to detail.
How to Apply:
To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website.
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