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Our client is seeking skilled CQV Resources to join a prominent company in the pharmaceutical industry based in the Genesis area. As a CQV Resource, you will play a crucial role in supporting the completion of essential documentation and ensuring the successful execution of various systems, including Aseptic Filling Line, Autoclave, and Manual Cleaning.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the CQV Resource will be varied; however, the key duties and responsibilities are as follows:
1. Review executed tests to ensure alignment with predefined protocols and GDP standards.
2. Verify supporting test documentation to ensure completeness and compliance with test expectations.
3. Progress and close out open defects (non-conformances) in alignment with Quality standards.
4. Manage Technical Change Control (TCR) processes from pre-execution to post-execution approval stages.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the CQV Resource, we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific or engineering discipline.
2. Proven industry experience in commissioning, qualification, and validation (CQV).
3. A working knowledge and practical experience with aseptic filling lines, autoclaves, and manual cleaning systems.
Key Words:
CQV / Commissioning / Qualification / Validation / Aseptic Filling / Autoclave / Manual Cleaning / Pharmaceutical / Documentation / Quality / Technical Change Control
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Our client is seeking skilled CQV Resources to join a prominent company in the pharmaceutical industry based in the Genesis area. As a CQV Resource, you will play a crucial role in supporting the completion of essential documentation and ensuring the successful execution of various systems, including Aseptic Filling Line, Autoclave, and Manual Cleaning.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the CQV Resource will be varied; however, the key duties and responsibilities are as follows:
1. Review executed tests to ensure alignment with predefined protocols and GDP standards.
2. Verify supporting test documentation to ensure completeness and compliance with test expectations.
3. Progress and close out open defects (non-conformances) in alignment with Quality standards.
4. Manage Technical Change Control (TCR) processes from pre-execution to post-execution approval stages.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the CQV Resource, we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific or engineering discipline.
2. Proven industry experience in commissioning, qualification, and validation (CQV).
3. A working knowledge and practical experience with aseptic filling lines, autoclaves, and manual cleaning systems.
Key Words:
CQV / Commissioning / Qualification / Validation / Aseptic Filling / Autoclave / Manual Cleaning / Pharmaceutical / Documentation / Quality / Technical Change Control
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
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