Stability QA Officer

 

Highly regarded and expanding Pharmaceutical Company.

12 Month Limited Tenure with a view to perm.

Excellent Career Opportunity.

A great opportunity has become available for a suitably qualified and experienced Stability / QA professional to join the Stability Department of this renowned pharmaceutical manufacturer. As a Stability / QA Officer your main responsibility will be the initiation and maintenance of post approval stability programs.

 

Reporting to the Stability Manager, your additional responsibilities will be as follows:

 

• Preparation of stability data documentation to ensure that all stability monitoring ????? ????? met.
• Review of current testing requirements for stability trials through liaison with internal and external customers.
• Assist in investigations of OOS results.
• Preparation of stability protocols to comply with customer requirements and regulatory standards.

 

In order to be eligible for the role, you will be required to have the following key criteria and personal attributes:

 

• Tertiary qualifications in Science preferably Chemistry.
• Strong working knowledge in stability data testing and review.
• Sound understanding of quality standards and requirements ie. cGLP / GMP and ICH.
• Superior verbal, written and technical communication skills.
• Significant experience in quality documentation.
• Exceptional organisational skills with a keen eye for detail.

 

This is an extraordinary opportunity for a candidate who is looking to grow and improve their career in an environment that is both congenial and supportive.

 

To submit your application in strict confidence, please apply online using the appropriate link below. Alternatively, please contact Voula Triantafillou on (??) ???? ???? quoting reference code TSVICVT.

 

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