Cleanroom Qualification/Validation Engineer (10-month contract)
Infos sur l'emploi
- Date de publication :24 octobre 2024
- Taux d'activité :100%
- Type de contrat :Durée indéterminée
- Lieu de travail :-, 1131 tolochenaz
Our long-time client Medtronic, is looking for a :, , Title : Cleanroom Qualification/Validation Engineer , Duration : 10 months, Location : Tolochenaz
Our long-time client Medtronic, is looking for a :
- Title : Cleanroom Qualification/Validation Engineer
- Duration : 10 months
- Location : Tolochenaz
Your mission
- Develop, validate, and implement methods for managing controlled environments.
- Establish controlled environment strategies, especially during changes in manufacturing lines or as part of improvement projects.
- Develop sampling plans for controlled environments, including particle measurements and utilities such as purified water, compressed air, gas, and others.
- Plan and oversee the qualification and annual requalification of cleanrooms, with a strong focus on classified areas.
- Write or maintain Process Failure Mode and Effects Analysis (pFMEA) documents.
- Responsible for defining and overseeing the cleaning validation strategy.
- Review biological and microbiological test results and conduct investigations when necessary.
- Coordinate microbiology testing with external suppliers to ensure timely and accurate results.
- Lead improvement projects aimed at optimizing laboratory processes.
- Manage non-conformities related to the controlled environment, laboratory procedures, or cleanroom qualifications.
- Ensure compliance with ISO standards such as ISO 14644 (Cleanrooms and associated controlled environments) and ISO 8573 (Compressed air).
- Coordinate and participate in activities during production shutdowns, including qualification/validation plan development and report writing, follow-up on activities, and non-conformity management.
Your profile
- Engineering degree (preferably in microbiology, HVAC, or cleanroom management).
- Minimum 2 years of experience in a similar role, particularly in cleanroom and classified area qualification and requalification.
- Experience in HVAC systems (purified water, compressed air, gas, etc.) and cleanroom operations.
- Proficiency in French and English.
- Strong background in managing non-conformities, qualification/validation reports, and continuous improvement.
- Hands-on experience in routine microbiological activities, including reviewing results and leading investigations.
Does that sound interesting to you ? Then apply now !
Contact
- Benoit Rochat