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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

Apply Here

About Arval

Revenue: Unknown / Non-Applicable
Size: Unknown
Type: Company - Public
Website: www.arval.es