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Senior Principal Validation Engineer
2 months ago
Curia is seeking a highly skilled Senior Principal Validation Engineer to join our team in Albuquerque, NM. As a key member of our validation team, you will be responsible for overseeing validation activities, managing projects, and ensuring compliance with regulatory requirements.
Key Responsibilities:- Develop and execute validation protocols and reports for equipment, process utility, test, and revalidations.
- Support department projects by assisting engineers, calibrations, and validations on ongoing projects.
- Provide leadership to contractors supporting the validation program.
- Ensure change controls, records, and procedures follow current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDPs).
- Review and write validation protocols, final reports, and summaries of work for release of equipment tested.
- Serve as validation liaison between the site and customers or regulatory agencies during facility audits.
- Bachelor's degree in Science, Engineering, or relevant field.
- 15 years of relevant experience in pharmaceutical validation (aseptic/sterile product facility).
- Experience with validation tools and processes, including temperature mapping and use of Kaye Validator.
- Experience with FDA and EU regulations for pharmaceuticals and validation requirements.
- A competitive salary and benefits package.
- The opportunity to work with a talented team of professionals.
- A dynamic and challenging work environment.
Curia is an Equal Opportunity Employer and welcomes applications from diverse candidates. We are committed to creating an inclusive and respectful work environment.