CQV Engineer

Work with Us
€560 - €640 per day
Belgium, Belgium
Contract
Job Reference: J5639462
Status: Open to Applications
Updated: 13/09/2024

Role Overview

We are currently looking for a CQV / C&Q Engineer to join a leading Pharmaceutical company based in the Walloon Region, Belgium. As the CQV / C&Q Engineer you will be responsible for performing Commissioning, Qualification and Process Engineering activities for a Biologics Fill Finish area and its associated equipment (e.g. Autoclaves).

This is a mission until the end of September 2025, with possible extension thereafter. For the right experience, this mission can offer an hourly rate of €70-80 per hour, 40 hours per week.

Key Duties and Responsibilities

Your duties as the CQV / C&Q Engineer will be varied however the key duties and responsibilities are as follows:

1. As the CQV / C&Q Engineer you will draft C&Q documents, coordinate review and approval following the approved VMP (Validation Master Plan).

2. As the CQV / C&Q Engineer you will provide guidance and manager suppliers with their C&Q activities, from design to field execution and summary report approval.

3. As the CQV / C&Q Engineer you will drive verification testing, protocol execution, walk-downs, verification of system drawings, design and operational testing, and troubleshoot as required.

4. As the CQV / C&Q Engineer you will plan, track, and report C&Q status and risks/issues for the selected system(s), taking corrective actions to ensure deadlines and milestones are achieved.

Role Requirements

To be successful in your application to this exciting opportunity as the CQV / C&Q Engineer we are looking to identify the following on your profile and past history:

1. Relevant degree in a Technical qualification at third level or equivalent in Engineering.

2. Extensive industry experience in Commissioning and Qualification / C&Q activities within a Biological / Biopharma manufacturing environment.

3. A working knowledge and practical experience with ISPE best practice, GAMP-5, Annex 15 GMP EU, ASTM E2500, and electronic execution.


Commissioning / Qualification / Process Engineer / Pharmaceutical / Biotechnology / Autoclave / Filling Line / CAPEX / GMP / ISPE / C&Q / Commissioning and Qualification / CQV / Process Engineering / Process Engineer / Validation Engineer / Validation Engineering / cGMP / GMP / Good Manufacturing Practice / Autoclaves / Fill and Finish / Filling Line / Filling Equipment / Pharmaceutical Filling / Biologics
Interested in this job? Apply for this position now!

Fabio Roque

Your Recruitment Consultant:

Fabio Roque

*Disclaimer*


Hyper 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 professionals and scientists. We look forward to helping you with your next career moves.
Sectors: Pharmaceutical, Biotechnology, Bioprocessing
Skills: Engineering - Commisioning, Engineering - Validation Contract, Quality Assurance - Validation, Graduates - Process / Chemical Engineering, Validation - Process Validation
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