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We are currently looking for a CQV & Validation Engineer to join a leading pharmaceutical engineering consultancy based in a hybrid role with travel across the UK and Ireland. As the CQV & Validation Engineer, you will be responsible for delivering high-impact pharmaceutical projects, ensuring compliance and excellence in sterile, biologics, and ATMP facilities.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the CQV & Validation Engineer will be varied; however, the key duties and responsibilities are as follows:
1. Lead or support CQV project delivery, from protocol development and execution (IQ/OQ/PQ) to final reporting.
2. Engage directly with client stakeholders in Engineering, QA, Validation, and MSAT to align on scope, risk, and compliance.
3. Participate in Process Risk Assessments (PRAs) and contribute to integrated solutions across process, utilities, and equipment.
4. Provide technical guidance on sterilisation, depyrogenation, SIP/CIP cycles, and thermal system mapping.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the CQV & Validation Engineer, we are looking to identify the following on your profile and past history:
1. Relevant degree in a related field.
2. Proven industry experience in pharmaceutical CQV, validation, or sterile utilities.
3. A working knowledge and practical experience with GMP environments, validation principles, and regulatory compliance (e.g., Annex 1 / FDA).
Key Words:
CQV / Validation Engineer / Pharmaceutical Engineering / Sterile Utilities / GMP Compliance / Annex 1 / FDA / Process Risk Assessment / SIP/CIP / Thermal System Mapping / Biologics
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.
We are currently looking for a CQV & Validation Engineer to join a leading pharmaceutical engineering consultancy based in a hybrid role with travel across the UK and Ireland. As the CQV & Validation Engineer, you will be responsible for delivering high-impact pharmaceutical projects, ensuring compliance and excellence in sterile, biologics, and ATMP facilities.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the CQV & Validation Engineer will be varied; however, the key duties and responsibilities are as follows:
1. Lead or support CQV project delivery, from protocol development and execution (IQ/OQ/PQ) to final reporting.
2. Engage directly with client stakeholders in Engineering, QA, Validation, and MSAT to align on scope, risk, and compliance.
3. Participate in Process Risk Assessments (PRAs) and contribute to integrated solutions across process, utilities, and equipment.
4. Provide technical guidance on sterilisation, depyrogenation, SIP/CIP cycles, and thermal system mapping.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the CQV & Validation Engineer, we are looking to identify the following on your profile and past history:
1. Relevant degree in a related field.
2. Proven industry experience in pharmaceutical CQV, validation, or sterile utilities.
3. A working knowledge and practical experience with GMP environments, validation principles, and regulatory compliance (e.g., Annex 1 / FDA).
Key Words:
CQV / Validation Engineer / Pharmaceutical Engineering / Sterile Utilities / GMP Compliance / Annex 1 / FDA / Process Risk Assessment / SIP/CIP / Thermal System Mapping / Biologics
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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