Pharmaceutical Validation Engineer
St. Louis, MO
Our client is a large Medical Device and Pharmaceutical manufacturer. They are in need of a validation engineer to qualify new equipment in a microbiological lab as well as validate a new lab system.
This individual will be performing qualification of 4 new incubators in a microbiological lab. This will include IQ OQ and PQ of all pieces of equipment as well as any other necessary documents. They will also requalify 8 existing incubators, and one new lab refrigerator. They will be writing and executing protocols and will need to hit the ground running. This person must also have experience writing and executing documentation for a non-viable particle counting system. They should have written trace matrix, urs, and protocols. They have Grade A through Grade D cleanrooms with 4-5 filling lines. They installed a non-viable particle counting system and need someone to validate it.
- Qualification of lab equipment
- Lab Instrumentation Qualification
- Documentation for Non-Viable Particle (NVP) system