Description
My client, a Global Biotechnology Organisation based in the North West, are seeking a Senior Quality Assurance/Validation Consultant for a interim contract which is likely to last a minimum of 6 months to start over the next 4-6 weeks.The ideal candidate will have experience of sterile aseptic manufacture, isolator technology as well as being familiar with the review and approval of IQ/OQ qualification documentation. A strong background in operational QA is essential.
Qualifications and Essential Skills:
- Educated to Degree level in Scientific fields
- Minimum 8-10 years GMP experience within the pharmaceutical industry
- Good knowledge of EU and US GMP regulations
- Strong communication and technical writing skills
- Project Management Experience
This is an excellent opportunity to work for an exciting and established organisation offering competitive daily rates.
If you are interested please contact Hemish Ilangaratne on . We also offer £200 worth of vouchers for any successful referrals.
Look forward to hearing from you.
Best regards
To find out more about Real please visit www.realstaffing.com