Job description
we are in the pharmaceutical industry and looking for Process Validation support for manufacturing of fill/finish products.
Day-to-Day Responsibilities
- we are looking for a process validation engineer who can generate process validation protocols, summary reports and understand what documentation is required from CQV through the process validation lifecycle.
- You should have a great understanding of what critical process parameters are vs. non-critical process parameters.
- It is required to be able to support PV readiness, complete risk assessments and own Process Validations from end to end.
- You will be providing the oversight of batch executions/manufacturing from a process validation perspective in order to be able to raise concerns throughout the process and correct as needed.
Job Types: Full-time, Contract
Pay: $50.00 per hour
Experience level:
- 5 years
Schedule:
- 8 hour shift
- Day shift
Work setting:
- In-person
Education:
- Bachelor's (Required)
Experience:
- process validation: 2 years (Required)
- CQV: 2 years (Required)
- Validation protocols: 1 year (Required)
- Critical process parameter: 1 year (Required)
- PV readiness: 1 year (Required)
Work Location: In person
About Arval
Revenue: Unknown / Non-Applicable
Size: Unknown
Type: Company - Public
Website: www.arval.es