Cleaning Validation

We have 12 month contracts for Cleaning Validation Engineers to join a leading global biopharma company in San Francisco. This company is currently undergoing large investment projects to increase manufacturing to meet the rise in global demand to treat rare genetic diseases.

The successful candidate will have experience in coordinating and executing Cleaning Validation site wide including worst case studies. You will generate protocols/reports/SOPs associated with validation studies. Along with this, you will participate in change control assessments and deviations investigations relating to cleaning. It will also be your duty to be involved in preparation and presentation of Cleaning Validation data during regulatory audits.

Skills:

• 3+ years’ experience in Cleaning Validation within the pharmaceutical / bio-pharmaceutical sector
• Sound understanding of GMP and pharmaceutical manufacturing
• Ability to review/approve other equipment qualification studies when required
• Demonstrate the ability to work to tight deadlines
• Be self motivated and driven with the ability to work under little supervision
• Must be eligible to work in the USA

If this role is of interest to you, apply now for immediate consideration.

The candidate must have the rights to work in the location stated in the job advert.

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