Hyper Recruitment Solutions
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QA Validation Manager

HertfordshirePermanent
£55,000 - £65,000 per annum
Job Reference: J5631373
Updated On: 24/04/2019
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Life Sciences, Science

Skills: Engineering - Validation Perm, Quality Assurance - Validation, Validation - Process Validation, Validation - Equipment Validation, Validation - Cleaning Validation, Validation - Facilities/Utilities Validation

Job Information

Role Overview

We are currently looking for a QA Validation Manager to join a leading company based in the Hertfordshire area. As the QA Validation Manager you will be responsible for organising and deploying resources effectively to deliver validation services to meet and exceed customer expectation. Further to this you will ensure compliance with all applicable regulatory and internal standards and industry best practices.

Key Duties and Responsibilities

Your duties as the QA Validation Manager will be varied however the key duties and responsibilities are as follows:

1. You will be responsible for ensuring the compliance of all validation activities at the of the facility, across all departments and ensure they all regulatory requirements.

2. You will maintain an ongoing dialogue with various departments to ensure documentation approval is effectively managed to meet dynamic and competing business priorities.

3. As the QA Validation Manager you will have oversight of commissioning, qualification and validation implementation to ensure consistent service delivery and systemic application of requirements across all validation departments.

4. You will continuously improve validation requirements whilst in alignment with industry best practices and stakeholder requirements.

Role Requirements

To be successful in your application to this exciting opportunity as the QA Validation Manager we are looking to identify the following on your profile and past history:

1. Relevant degree in a Science or Engineering related discipline or equivalent experience.

2. Proven industry experience in Pharmaceutical Sterile Process validation, or other validation activities within a sterile manufacturing environment.

3. A working knowledge and practical experience with pharmaceutical validation principles and legislation as well as a demonstrable understanding of risk and science-based tools and their practical application.


Key Words: Validation | QA | Manager | Pharmaceutical | Biopharmaceutical | Manufacturing | GxP | EHS | Quality | Engineering | Production | Equipment | Process | Facilities | Utilities | Continuous Improvement |
Sarah Adeniji
Your Recruitment ConsultantSarah Adenijisarah.adeniji@hyperec.com
DisclaimerHyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.