9 beste Stellen als qualification validation (cqv) engineer – aktuell auf Personalsuche

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Commissioning Qualification Validation (CQV) Engineer
GXP Consulting Switzerland —Epalinges, VD
Able to develop and execute DQ, FAT, SAT, OQ, PQ, develop SOPs, create final reports and author validation and quality policies, procedures and guidelines under…
CQV Engineer / Qualification & Validation Engineer 80-100% (m/f/d)
Lonza —Visp, VS
Coordinate efforts between internal teams and external service providers and suppliers to ensure seamless project execution.
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Commissioning Qualification Validation (CQV) Engineer

GXP Consulting Switzerland
Epalinges, VD

Jetzt bewerben

Details zur Stelle

Qualifikationen

Französisch
Schreibfähigkeiten
Englisch
Master
HLK
Kundensupport
Zeitmanagement

Vollständige Stellenbeschreibung

Did you ever want to work for a company placing human at the heart of its DNA? Are you ready to make a difference? Do you feel excited about the opportunity to collaborate and share your expertise with our industry leaders? YES? SO DO WE!

GXP CONSULTING Switzerland is a Swiss company with a passionate team of Life Sciences professionals. Since 2014 we deliver outstanding industry’s expertise and support to our clients in the complete range of product life cycle : R&D, Engineering, Quality Assurance, Qualification / Validation, Regulatory Affairs, Operational Excellence, Manufacturing, Maintenance and Project Management.

Are you passionate about quality and interested in GxP environments?

Join a team where your qualification/validation skills will make a real impact on patients' lives.

About the job:

Establish and execute qualification protocols; IQ, OQ, PQ
Write technical documentation including equipment risk assessments (critical component assessments), Validation Plans, Requirement Tractability Matrices and qualification reports
Participate in the qualification of systems such as HVAC, Clean Utilities, process or lab equipment
Coordinate qualification execution activities, including external vendors, internal departments, organizing materials, etc.
Manage associated qualification deviations & CAPAs, including opening, resolution (with Supplier) and closure
Contribute to risk assessments and quality improvements

About you:

Master’s degree in sciences or engineering or equivalent in experience.
At least 4 years of experience in equipment qualification (IQ, OQ, PQ)
Previous work experience in either the Pharmaceutical, Biotech or Medical Devices sector
Good analytical, organizational, time management and problem-solving skills.
Good writing skills. Able to develop and execute DQ, FAT, SAT, OQ, PQ, develop SOPs, create final reports and author validation and quality policies, procedures and guidelines under direct or indirect supervision of the Senior engineering team.
Solid knowledge of current FDA and EU regulations and best practices
French with good knowledge of English

About us:

Human-sized company with great colleagues from a large diversity of cultural and professional backgrounds
We do care about our people, communicate openly and value feedback
Work as a team where every member is valued and appreciated
Opportunity to contribute to ambitious projects within an international and multicultural environment that fosters innovation, collaboration, and professional growth.
Continuous learning and development opportunities via internal or external training and workshops
Competitive salary package in line with industry practice together with exceptional employment benefits

At GXP Consulting Switzerland everyone contributes to our joint success and grows individually!

If you also share the same passion and values, we will be glad to hear from you! Please send us your application.

Jetzt bewerben

Erweiterte Suche

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