CQV Specialist

Are you ready for a change? Tired of the same routine? Join our team and make your mark in the industry!
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Title: CQV Specialist
Location: Visp, Switzerland
Rate: Open
Openings: 3 Specialists
Contract/Perm: Contract (6-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.

Responsibilities:

• The Commissioning Qualification Validation engineer carries out a variety of tasks related to the validation of equipment and facilities.
• The scope of activities includes the coordination on the installation of equipment, drafting the IQ/OQ/PQ protocols, execution of the IQ/OQ/PQ and documenting the results according cGMP requirements.

Key Accountabilities:

• The CQV Engineer will be involved in all validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others.
• The validation documentation deliverables include URS, DQ, FMEA, Risk Assessments, FAT, SAT, Protocols (IQ, IOQ, OQ, PQ).
• Prepare validation documents.
• Execution of IQ/OQ and PQ for equipment, systems and utilities.
• Write reports of completed validation activities.
• Work to identify efficiencies in the validation program approach.
• Work to apply lessons learned and stay informed of industry regulatory changes as it applies to equipment / facility validation.
• Perform assigned Quality Systems activities including Document Management system, Change Control, Non-Conformities, and CAPA's.
• Writing and/or revising procedures applicable to the Engineering activities.
• Support the Engineering group to prepare the validation, requalification, and maintenance program.
• Perform other duties as assigned.

Key Skills and Requirements:

• Bachelor's Degree in Science or Technical field.
• Proficient in English.
• Significant experience in the pharmaceutical industry, typically gained over several years, demonstrating a deep understanding and expertise in the field.
• Excellent technical writing skills and the ability to document all work in a thorough, accurate and timely manner.
• Excellent written and oral communication skills and the ability to work interdepartmentally in an effective manner to carry out daily duties.
• Excellent organizational and time management skills.

If you are having difficulty in applying or if you have any questions, please contact Saulge Hubert

S.Hubert@Proclinical.com
CH: +41 61 508 7073
WhatsApp: +41 61 508 7073

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.