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in La Verne, CA

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Hours Full-time, Part-time
Location La Verne, CA
La Verne, California

About this job

Implements process validation, primary packaging validation, cleaning validation, equipment validation and revalidation activities to meet cGMP requirements.

Duties:
∙ Author validation protocols and technical reports (e.g., Pre Validation Studies, Performance Qualifications, Requalifications, Annual Monitoring Batches)
∙ Perform process qualification for new equipment and new technologies.
∙ Author complex validation protocols and technical reports (e.g. launches, transfers, weak point remediation).
∙ Participate in transfers and launches. Contribute to provide experimental data obtained during the validation activities, which will be used to prepare the related registration documentation.
∙ Perform or oversee risk assessments for Validation.
∙ Participate or lead improvement and remediation of products.
∙ Provide Validation oversight review and approval of Production documentation, e.g. Master Batch Records (MBRs) and Standard Operating Procedures (SOPs).
∙ Provide Validation oversight review and approval of change control documentation.

 

Experis is an Equal Opportunity Employer (EOE/AA)