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Validation Engineer
Full Time
Le Sueur, Minnesota, United States (This job is on-site)
Job description
Role Summary:
- Review, plan, schedule and organize validation projects for new and existing areas, including manufacturing equipment, processes, plant systems, storage facilities and equipment.
- Develop and implement all necessary standard operating procedures for validation of plant processes, equipment installation and operational qualification (IQ/OQ), performance qualification (PQ), requalification and revalidation of critical systems and utilities.
- Design IQ/OQ/PQ and validation campaigns, develop, prepare and write the protocols for process validation, equipment validation, cleaning validation, IQ/OQ and performance qualification.
- Coordinate validation and IQ/OQ/PQ activities with production, quality control laboratories and outside contractors providing leadership, training and guidance.
- Review and analyze moderately complex analytical and physical data generated from validation activities. Write validation final reports that present, summarize and offer conclusions on the validity of the process based on the results of the analysis and obtain necessary approvals on a timely basis.
- Coordinate the facility qualification program by preparing the protocols, monitoring the execution, auditing the results, and assisting production in resolving any identified problems.
- Recommends validation approaches / strategies, priorities, and resources required. Accountable for accuracy and integrity of protocols, reports and documentation generated to meet regulatory authorities, accountable for meeting critical deadlines for complex projects.
- Schedule and coordinate calibration events. Log and maintain calibration certificates and records both hard copies and operation of the Blue Mountain RAM program in the Irwindale facility.
- Assess proper functionality of the Getinge Sterilizer by performing weekly autoclave cycles.
- At least 5 years relevant experience in a regulated pharmaceutical industry.
- Minimum of Bachelors of Science in science or related field.
- Experience working in a validation role.
- Knowledge of validation strategies and execution techniques, validation requirements and regulatory expectations for GMP compliance.
- Familiarity with maintenance processes, PM management and general equipment operations.
- Experience and knowledge of Kaye validator.
- Must possess strong customer focus and quality mind set.
- Is a champion of compliance while balancing business results.
- Strong command of the English language; written and orally.
- Blue Mountain calibration and asset management system experience.