A leading Biopharmceutical company are actively recruiting a CQV Engineer to join their team in Limburg, The Nethelands. As the CQV Engineer, you will play a crucial role in ensuring the quality and compliance of facilities, utilities, and processes.
This is an initial 6 month contract with possible extension.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the CQV Engineer will be varied; however, the key duties and responsibilities are as follows:
1. As the CQV Engineer, you will prepare validation documents, including URS, DQ, FMEA, Risk Assessments, FAT, SAT, and Protocols (IQ, IOQ, OQ, PQ).
2. As the CQV Engineer, you will execute IQ/OQ and PQ for equipment, systems, and utilities.
3. As the CQV Engineer, you will write comprehensive reports of completed CQV activities.
4. As the CQV Engineer, you will stay informed of industry regulatory changes as they apply to equipment and facility validation.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the CQV Engineer , we are looking to identify the following on your profile and past history:
1. Relevant degree in a related subject area.
2. Proven industry experience within a validation/CQV role. We are looking for an established CQV Engineer within the Pharma/Biopharma industries.
3. A working knowledge and practical experience with GMP environments, GDocP, Data Integrity, and ALCOA++.
Key Words: CQV Specialist / Commissioning / Qualification / Validation / GMP / GDocP / Data Integrity / ALCOA++ / Risk Assessment / Technical Documentation / Engineering Validation
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.
This is an initial 6 month contract with possible extension.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the CQV Engineer will be varied; however, the key duties and responsibilities are as follows:
1. As the CQV Engineer, you will prepare validation documents, including URS, DQ, FMEA, Risk Assessments, FAT, SAT, and Protocols (IQ, IOQ, OQ, PQ).
2. As the CQV Engineer, you will execute IQ/OQ and PQ for equipment, systems, and utilities.
3. As the CQV Engineer, you will write comprehensive reports of completed CQV activities.
4. As the CQV Engineer, you will stay informed of industry regulatory changes as they apply to equipment and facility validation.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the CQV Engineer , we are looking to identify the following on your profile and past history:
1. Relevant degree in a related subject area.
2. Proven industry experience within a validation/CQV role. We are looking for an established CQV Engineer within the Pharma/Biopharma industries.
3. A working knowledge and practical experience with GMP environments, GDocP, Data Integrity, and ALCOA++.
Key Words: CQV Specialist / Commissioning / Qualification / Validation / GMP / GDocP / Data Integrity / ALCOA++ / Risk Assessment / Technical Documentation / Engineering Validation
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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