QA VALIDATION SPECIALIST
| Employment Type | Permanent |
|---|---|
| Location | Hampshire , Hampshire |
| Industry Sector | Manufacturing |
| Start Date | %tehcareerengineer_startdate% |
| Salary/Rate | ŁNeg + Benefits |
| Reference | TP756 |
| Date Advertised | 30-09-2008 - 14:22 |
This vacancy is out of date and no longer accepting applications.
Description
Quality Assurance Validation Specialist invited to join World-Class, state-of-the-art pharmaceutical manufacturing facility in Southern Hampshire. Duties will include Quality support and Validation to Engineering and IS based projects. Candidates will have proven experience of Quality Assurance and Validation in a similar environment, including Engineering, Automation and IS systems. Experience in a cold-chain / food / pharma production background would be beneficial.
Quality Assurance Validation Specialist invited to join World-Class, state-of-the-art pharmaceutical manufacturing facility in Southern Hampshire. Duties will include Quality support and Validation to Engineering and IS based projects. Candidates will have proven experience of Quality Assurance and Validation in a similar environment, including Engineering, Automation and IS systems. Experience in a cold-chain / food / pharma production background would be beneficial.
Accountabilities:
Leadership
•To act as the Quality Lead for Validation, Engineering and IS. To include IS and Engineering Projects.
•To make decisions appropriate to level of knowledge and escalate as necessary.
•To provide information on current regulatory and company standards that must be met to achieve and maintain compliance.
•To ensure that validation studies are executed in accordance with cGMP, regulatory requirements, corporate policies, site validation procedures, validation master plans and protocols
•To ensure that all validation activities are carried out and reported in a timely manner.
•To review and approve Validation, Engineering and IS documentation.
•To participate in supplier assessments for Engineering and IS equipment and services and for Validation services.
•To participate in Risk Based decision making.
•Ensure site activities within the function scope are in line with corporate and local standards, meet current cGMP and licence requirements.
•To effectively communicate and mentor staff within project and other teams to ensure that the need for compliance is clearly understood.
•To provide support and input to Management to work towards a common validation process.
•To facilitate, encourage and coordinate continuous improvement with respect.
•To work with Communities of Practice
Education, Experience and Qualifications:
Educated to HNC / HND level in an appropriate discipline (e.g. Science, Technical or Life Science) with a broad technical/educational skills base and substantial related experience or 5 years experience in a similar role with relevant experience.
