Posted in Information Technology 4 days ago.
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Location: Raleigh, North Carolina
Pharmaceutical Research Associates, Inc.
(All) | US-KS-Lenexa
Responsible for initiation, organization and review of all necessary (periodic) validation activities, in order to secure GxP compliance of all equipment and systems used.
Assist in preparing Validation Files.
Executing and reporting Periodic Review
Assist in writing, reviewing and finalizing Validation Documentation.
Performing tests as described in the Validation Plan.
Evaluating already validated systems.
Assist tracking information about validations in system inventory.
Assist in improvement projects/corrective and preventive actions.
Participating in the continuous improvement of processes and quality.
Assist in (re)writing SOP's, Work Instruction and reference documents.
Identifying and reporting quality issues regarding applications and systems
Bachelor degree in relevant field
1 year relevant experience
Read, write and speak fluent English; fluent in host country language required.
To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.
PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.