• jobs
  • 4 weeks ago

jobs description

The Validation Engineer will work with our Clients and be responsible for preparing and executing validation documents. Demonstrate an understanding of cGMP. Individuals must represent the company and division at client sites and interact confidently with clients, contractors, management and peers.

Essential Duties include, but are not limited to:
• Develop Validation Plan (VMP)
• Develop validation protocols (IQ, OQ, PQ, TMV, CSV) for process and/or equipment.
• Develop Manufacturing Standard Operating Procedures.
• Develop Test Methods.
• Develop Preventive Maintenance Procedures.
• Execute and Planning Validation Activities.
• Coordinate Equipment Installation and Calibrations.
• Develop and system routing of Change Control and Change Request.
• Agile system management.
• Compile/Analyze analytical validation data and test results using statistical methods as MINITAB.
• Assure systems/processes consistently result in products or processes that meet established specifications and... quality standards.

• Bachelor's degree in Chemical Engineering, Industrial Engineering, Mechanical Engineering, Biotechnology or related sciences.
• Minimum of 2-5 years of validation experience in pharmaceutical and medical device industry.

Job Types: Full-time, Contract

Pay: $30.00 - $45.00 per hour

Expected hours: 40 per week

Experience level:
• 2 years

• Monday to Friday
• Weekends as needed

Work setting:
• In-person

Work Location: In person
Puerto Rico


Apply - Validation Engineer Puerto Rico