Freelance Sterilisation Expert
Firmenname für PREMIUM-Mitglieder sichtbar
- April 2024
- Dezember 2024
- D-Erlangen
- auf Anfrage
- Remote
- 03.04.2024
- JN -042024-99275_1712131471
Projekt Insights
Projektbeschreibung
- Sterilisation Expert
- 7 Month contract
- Hybrid
I am currently working with an existing customer of mine who are situated deeply in the Life Science industry they offer services to Medical Devices, Pharmaceutical and Healthcare Customers. In this project you will be working on the quality of existing products and also products during the design and development phase.
Responsibilities:
* Ensure contract sterilization processes comply with regulatory standards.
* Manage and develop sterilization SMEs.
* Provide QMS training for sterilization procedures.
* Oversee compliance and handle product disposition for non-conformities.
* Coordinate timely validations and qualifications.
Qualifications:
* Experience in sterilization principles and controls.
* Proficiency in FDA QSRs, ISO 13485, and medical device regulations (Desirable).
* Strong technical knowledge in controlled manufacturing environments.
* Lead Auditor (Desirable)
* English Language
* Bachelors in Microbiology or necessary experience within this field
* Must be based in Europe
If you are interested please send your CV.
- 7 Month contract
- Hybrid
I am currently working with an existing customer of mine who are situated deeply in the Life Science industry they offer services to Medical Devices, Pharmaceutical and Healthcare Customers. In this project you will be working on the quality of existing products and also products during the design and development phase.
Responsibilities:
* Ensure contract sterilization processes comply with regulatory standards.
* Manage and develop sterilization SMEs.
* Provide QMS training for sterilization procedures.
* Oversee compliance and handle product disposition for non-conformities.
* Coordinate timely validations and qualifications.
Qualifications:
* Experience in sterilization principles and controls.
* Proficiency in FDA QSRs, ISO 13485, and medical device regulations (Desirable).
* Strong technical knowledge in controlled manufacturing environments.
* Lead Auditor (Desirable)
* English Language
* Bachelors in Microbiology or necessary experience within this field
* Must be based in Europe
If you are interested please send your CV.
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