Similar posts
CQV engineer
- Contract
- Manufacturing
- Switzerland
Proclinical is seeking a CQV Engineer to join our client's team on a contract basis. In this role, you will focus on the validation of equipment and facilities, ensuring compliance with cGMP requirements. Your expertise will be crucial in coordinating equipment installation and executing validation protocols.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
- Coordinate installation of equipment and draft IQ/OQ/PQ protocols.
- Execute IQ/OQ/PQ and document results according to cGMP standards.
- Engage in validation activities for facilities, utilities, and processes.
- Prepare and manage validation documentation including URS, DQ, FMEA, and risk assessments.
- Write reports on completed validation activities.
- Identify efficiencies in validation programs and apply industry regulatory changes.
- Perform quality systems activities such as document management, change control, and CAPA's.
- Write or revise procedures related to engineering activities.
- Support the engineering team in preparing validation, requalification, and maintenance programs.
- Perform other duties as assigned.
Key Skills and Requirements:
- Bachelor's degree in science or Technical field.
- Proficiency in English.
- Strong technical writing skills for thorough and accurate documentation.
- Excellent communication skills for effective interdepartmental collaboration.
- Strong organizational and time management abilities.
If you are having difficulty in applying or if you have any questions, please contact Emile De Beer at e.debeer@proclinical.com.
Apply Now:
If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, 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.
Related jobs
Highly Competitive
Utrecht, Netherlands
Proclinical is seeking a dedicated CMC Specialist to join our client's team for a permanent role in The Netherlands.
Highly Competitive
Visp, Switzerland
Proclinical is currently working alongside a contract manufacturing organisation to recruit for a Material Planner to be based in Visp, Switzerland.
Highly Competitive
Solothurn, Switzerland
Proclinical is currently working alongside a biotechnology company to recruit for a dedicated Senior Manager, Global Upstream MSAT. This is a permanent position based in Solothurn, Switzerland.
Highly Competitive
Stein, Schweiz
Proclinical is currently working alongside a Contract Manufacturing Organisation to recruit for a CQV Engineer GMP Warehouse. This temporary contract position is based in Stein, Switzerland.
Highly Competitive
Stein, Schweiz
Proclinical is seeking an Engineer Lead to join our partner's team on a contract basis.
Highly Competitive
Visp, Schweiz
Proclinical is currently working alongside a pharmaceutical company to recruit for a 3D CAD Coordinator. This is a temporary contract position based in Visp, Switzerland.
Highly Competitive
Reykjavík, Iceland
Proclinical is collaborating with a biotech company to recruit a Senior DSP for their team in Iceland.
Highly Competitive
Reykjavík, Ísland
Proclinical is collaborating with a biotech company currently seeking a Senior Biotechnologist to join the team in Iceland.
Highly Competitive
Visp, Switzerland
Proclinical is currently working alongside a contract manufacturing organisation to recruit for a Warehouse Operator. This temporary contract position is based in Visp, Switzerland.
Highly Competitive
Visp, Switzerland
Proclinical is seeking a Process Engineer to join our client's team in Switzerland.