Weil Group Inc is seeking a Validation Specialist with a focus on Performance Qualification (PQ) and equipment characterization in a GMP-regulated environment in Juncos, PR. The ideal candidate will have hands-on experience in validation and aseptic operations, with a strong ability to work independently and manage multiple priorities
Job Summary
The role involves executing performance qualification and equipment characterization protocols for critical aseptic manufacturing systems.
Candidates must operate effectively within strict cGMP standards while managing materials and documentation for E-Beam tunnels and filling equipment.
This position requires flexibility to support parallel workstreams with rotating schedules and extended hours in a fast-paced environment.
Matching Summary
Match Score: 85
Weil Group Inc is seeking a Validation Specialist with a focus on Performance Qualification (PQ) and equipment characterization in a GMP-regulated environment in Juncos, PR. The ideal candidate will have hands-on experience in validation and aseptic operations, with a strong ability to work independently and manage multiple priorities.
Skills & Requirements
Must-have
Execute PQ protocols for E-Beam and isolators
Operate in aseptic and controlled environments
Troubleshoot equipment characterization issues
Utilize LIMS, Kneat, and Batch Record systems
Work rotating schedules under high pressure
Nice-to-have
Experience with decontamination cycles
Comfortable navigating fast-paced projects
Strong problem-solving and communication skills
Key Requirements
Bachelor's degree in Science or Engineering
1-3 years experience in validation or aseptic operations
Availability for rotating schedules and extended hours