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Our client is seeking a dedicated Commissioning and Qualification Specialist to join a prominent company in the Pharmaceutical/Biotechnology industry based in the Brussels area. As the Commissioning and Qualification Specialist, you will play a crucial role in ensuring the successful execution and compliance of various systems and equipment.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Commissioning and Qualification Specialist will be varied however the key duties and responsibilities are as follows:
1. Accountable for the team drafting or supporting the document drafting by a partner or supplier, coordinating review and approval of applicable C&Q documents (QRA/DV/RTM/FAT/SAT/IOV/VSR) following approved VMP and SLIA.
2. Act as C&Q Subject Matter Expert and Compliance, providing guidance and managing supplier and all C&Q activities for the system(s), from design to field execution and summary report approval.
3. Drive verification testing, protocol execution, walk-downs, verification of system drawings, design and operational testing, and troubleshoot as required. Conduct deviation investigation and resolution for problems and issues encountered during field execution activities.
4. Responsible for the planning, tracking, and reporting of C&Q status and risks/issues for the selected system(s). Take appropriate corrective actions as required to ensure deadlines and milestones are achieved.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Commissioning and Qualification Specialist we are looking to identify the following on your profile and past history:
1. Relevant degree in Engineering or a related field.
2. Extensive industry experience in Commissioning and Qualification for Pharmaceutical/Biotechnology projects.
3. A working knowledge and practical experience with automation-related aspects of equipment.
Key Words:
Commissioning / Qualification / Pharmaceutical / Biotechnology / C&Q Specialist / Compliance / Protocol Execution / System Drawings / Verification Testing / Equipment Start-up / Quality Risk Assessment
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 a dedicated Commissioning and Qualification Specialist to join a prominent company in the Pharmaceutical/Biotechnology industry based in the Brussels area. As the Commissioning and Qualification Specialist, you will play a crucial role in ensuring the successful execution and compliance of various systems and equipment.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Commissioning and Qualification Specialist will be varied however the key duties and responsibilities are as follows:
1. Accountable for the team drafting or supporting the document drafting by a partner or supplier, coordinating review and approval of applicable C&Q documents (QRA/DV/RTM/FAT/SAT/IOV/VSR) following approved VMP and SLIA.
2. Act as C&Q Subject Matter Expert and Compliance, providing guidance and managing supplier and all C&Q activities for the system(s), from design to field execution and summary report approval.
3. Drive verification testing, protocol execution, walk-downs, verification of system drawings, design and operational testing, and troubleshoot as required. Conduct deviation investigation and resolution for problems and issues encountered during field execution activities.
4. Responsible for the planning, tracking, and reporting of C&Q status and risks/issues for the selected system(s). Take appropriate corrective actions as required to ensure deadlines and milestones are achieved.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Commissioning and Qualification Specialist we are looking to identify the following on your profile and past history:
1. Relevant degree in Engineering or a related field.
2. Extensive industry experience in Commissioning and Qualification for Pharmaceutical/Biotechnology projects.
3. A working knowledge and practical experience with automation-related aspects of equipment.
Key Words:
Commissioning / Qualification / Pharmaceutical / Biotechnology / C&Q Specialist / Compliance / Protocol Execution / System Drawings / Verification Testing / Equipment Start-up / Quality Risk Assessment
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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