Design, develop, test, and evaluate integrated systems for handling efficient pharmaceutical production processes.
REQUIREMENTS:
- Master's Degree (or U.S. equivalent) in Validation Engineering, Industrial Engineering or related field + 2 years of experience in Validation & Process Engineering in pharmaceutical industry
OR
- Bachelor's Degree (or U.S. equivalent) in Validation Engineering, Industrial Engineering or related field + 5 years of experience in Validation & Process Engineering in pharmaceutical industry
Must have experience with:
- Cleaning validation, process & utility systems validation, temperature mapping, manufacturing equipment qualification & validation
- Hands-on experience in planning & creation of schedules for preventive maintenance & calibration of critical equipment & instruments used in utility & production area AHU & RTU
- Hands-on experience obtaining documentation necessary for change control deviations & other GMP docs & the respective revised docs for accuracy & completeness
- Knowledge of validation documentation for manufacturing packaging & facility equipment (HVAC, RTU, Utilities) & systems according to the GAMP4 validation Life cycle (URS, DS, Software & Hardware) Commission FAT IQ OQ PQ & reports
- Must have experience in the successful execution of IQ, OQ, PQ of equipment & validation of plant utilities
Schedule: 40 hours/week: Monday-Friday, 9-5
Must have authorization to work legally in U.S.
To be considered, please visit Glenmark Pharmaceuticals' career site at https://glenmarkpharma-us.com/careers-at-glenmark/career-search/ create profile & submit resume. Job# 20240105
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