Full-time
Cleaning Validation Engineer- Pharma
Posted by Process Engineering Specialists • Singapore, SG.01, Singapore
About the Role
PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.
With offices across Europe, Asia and US, our core focus is on consistently delivering high-quality outcomes for our multinational clients.
This focus, and our people's experience in delivering consistent quality results for our clients over the past 20 years has been key to our success to date.
We are currently looking for CQV Engineers to join us on a permanent role to help us deliver various projects in the Life Sciences Industry.
Key Attributes/Responsibilities:
We are currently looking at cleaning validation engineer with 3-5 years experience
Execute cleaning validation protocols and reports for GMP manufacturing equipment.
Develop cleaning validation strategies including worst-case product selection and sampling plans.
Perform swab and rins...
With offices across Europe, Asia and US, our core focus is on consistently delivering high-quality outcomes for our multinational clients.
This focus, and our people's experience in delivering consistent quality results for our clients over the past 20 years has been key to our success to date.
We are currently looking for CQV Engineers to join us on a permanent role to help us deliver various projects in the Life Sciences Industry.
Key Attributes/Responsibilities:
We are currently looking at cleaning validation engineer with 3-5 years experience
Execute cleaning validation protocols and reports for GMP manufacturing equipment.
Develop cleaning validation strategies including worst-case product selection and sampling plans.
Perform swab and rins...
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