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Validation Engineer - Pharma
Eingestellt von Experis AG
Gesuchte Skills: Engineer, Client
Projektbeschreibung
Validation Engineer
Pharma environment - 40 Hours per Week
On behalf of our client, one of the biggest pharmaceutical players based in Solothurn, we are looking for a Validation Engineer with expert knowledge in functional and physical test method validation.
This is a challenging, contracting position, starting ASAP until middle of the year.
In this position as Validation Engineer you will be responsible for the test method validation processes to ensure the conformity. Additionally you will create a new validation master list, identify anomalies and find new approach to remediate the test method validation in place.
YOU BRING TO THIS ROLE:
- Minimum of 2 years' experience as VALIDATION ENGINEER
- Minimum of 2 years' experience in the PHARMA ENVIRONMENT
- Profound experience in functional and physical test method validation
- Knowledge in MANUFACTURING and MEDICAL DEVICES production processes
- Knowledge in 21 CFR 820, 21 CFR 11, ISO 13485, ISO 9001 and GHFT
- Work experience in a GXP and FDA-regulated environment
- Understanding of SIX SIGMA, Green belt certification or higher is a plus
- MSA for mechanical industries, metrology and calibration
- Fluent in ENGLISH AND GERMAN,any additional language is an advantage
If you are an energetic, highly motivated individual and currently looking for a challenging new position that applies to your skills, then we look forward to receive your application!
Are you a Validation Engineer and still interested but not quite ready to click on the below apply button, then why don't you call JULIE MACKERER?
Pharma environment - 40 Hours per Week
On behalf of our client, one of the biggest pharmaceutical players based in Solothurn, we are looking for a Validation Engineer with expert knowledge in functional and physical test method validation.
This is a challenging, contracting position, starting ASAP until middle of the year.
In this position as Validation Engineer you will be responsible for the test method validation processes to ensure the conformity. Additionally you will create a new validation master list, identify anomalies and find new approach to remediate the test method validation in place.
YOU BRING TO THIS ROLE:
- Minimum of 2 years' experience as VALIDATION ENGINEER
- Minimum of 2 years' experience in the PHARMA ENVIRONMENT
- Profound experience in functional and physical test method validation
- Knowledge in MANUFACTURING and MEDICAL DEVICES production processes
- Knowledge in 21 CFR 820, 21 CFR 11, ISO 13485, ISO 9001 and GHFT
- Work experience in a GXP and FDA-regulated environment
- Understanding of SIX SIGMA, Green belt certification or higher is a plus
- MSA for mechanical industries, metrology and calibration
- Fluent in ENGLISH AND GERMAN,any additional language is an advantage
If you are an energetic, highly motivated individual and currently looking for a challenging new position that applies to your skills, then we look forward to receive your application!
Are you a Validation Engineer and still interested but not quite ready to click on the below apply button, then why don't you call JULIE MACKERER?
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Ingenieurwesen/Technik