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Our company is looking for Quality Engineers/Specialists to support upcoming projects in the nature of equipment and software validation. The selected candidates will review and approve Qualification Protocols and Reports for automated manufacturing equipment and software. He/she may also support process validation activities by performing Characterization studies and reviewing and approving process validation protocols. May develop, review or revise Procedures. Project duration is scheduled to 8+ months.
Requisitos - Requirements
Bachelor's degree in Science or Engineering, preferably. 3+ years of proven experience developing or reviewing qualification protocols for automated manufacturing equipment and software within the pharmaceutical or medical devices industries. Hands-on experience in Process validation and Statistical knowledge is a PLUS. Experienced reviewing or developing SOPs and Calibration, Maintenance and Lockout Tag-out Procedures. Able to handle multiple tasks at the same time and work under minimum supervision. Good Verbal and Written Communication skills in both, English and Spanish. Interested candidates must show proven experience in the required skills in order to be considered. Please submit resume in Word format for evaluation.