Are you ready for a change? Tired of the same routine? Join our team and make your mark in the industry!
CQV Engineer - Visp, Switzerland - Contract of 11 months
Join the team and be part of an innovative company that values inclusion, growth, and impact. Our dynamic work environment offers brilliant opportunities for advancement. We're seeking talented and driven individuals who share our passion for making a difference within the Life Science industry.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Key responsibilities:
As a CQV Engineer, you will be responsible for the qualification and validation of process engineering equipment and facilities. They make a significant contribution to the ongoing optimisation of processes, systems and internal procedures. You will be jointly responsible for ensuring the necessary technical knowledge of the plant personnel and the engineering groups including:
- Preparation of commissioning and qualification documents for new plants, as well as the supervision of conversion, expansion and new construction projects; this is broken down into PQs on new construction projects for critical systems and SLC support of all systems after go-live
- Support of deviations, changes (GEP and GMP), as well as CAPAs
- Coordination of internal groups, as well as external service providers and suppliers
- Responsibility for the presentation of the qualification documents during audits and inspections
- As a Quality Manager, you will be responsible for the qualification and validation of process engineering equipment and facilities.
- You will be responsible for the professional planning and implementation of qualification and validation activities resulting from projects and plant adjustments during the system life cycle of the plants. They make a significant contribution to the ongoing optimisation of processes, systems and internal procedures. They are jointly responsible for ensuring the necessary technical knowledge of the plant personnel and the engineering groups.
- Preparation of commissioning and qualification documents for new plants, as well as the supervision of conversion, expansion and new construction projects. This is broken down into PQs on new construction projects for critical systems and SLC support for all systems after go-live
- Support of deviations, changes (GEP and GMP), as well as CAPAs
- Coordination of internal groups, as well as external service providers and suppliers.
- Responsible for presenting the qualification documents during audits and inspections
- Mostly project support as a qualification specialist
Requirements:
- Degree from a technical college (HF) / university of applied sciences (FH) or university degree
- Several years of professional experience in a regulated environment with regard to commissioning, qualification and validation, e.g. refrigerators and freezers, clean media, clean rooms, as well as process engineering equipment
- Independent and flexible working with a good communication style, as well as structured, focused and well-organized work behaviour and also open to new ideas, agile and proactive
- Good knowledge of Microsoft Office is required, knowledge of COMOS (Plant Engineering Software Solution), DMS, TrackWise and SAP is an advantage
- German (fluent in written / oral), as well as English (good written / oral skills).
If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at A.Bennett@Proclinical.com or +41 61 563 3019
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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