Job Description
QUALITY ASSURANCE SPECIALIST
We're on the lookout for QA professionals!
Do you have Quality experience within Biopharmaceuticals?
As a Quality Assurance Specialist, you will assist in setting up the company Quality Management System (QMS).
You will support the review of all batch related documentation.
You will support customer and regulatory audits.
You will ensure compliance to GMP & GLP standards.
You will approve validation documents.
You will ensure that materials are the correct quality and sourced from approved suppliers.
Skills and Experience:
HND or above in Biological subject OR 5yrs+ experience in QA.
Minimum of 1 years' experience in QA/QC with Biopharmaceuticals or Pharmaceuticals.
Strong knowledge of GMP & GLP.
Experience in batch review, approval of validation documents, change control, deviations, internal audits, presenting metrics.
Experience in early phase GLP is advantageous.
Salary: Competitive (dependent on experience)
Location: Chester
Permanent - Full Time
APPLY NOW! Contact Jacob Golding for further details - 
0161 839 5353 - jacob@emp-sol.com
