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Process Validation Specialist

1 month ago

Glendale, Arizona, United States Azzur Group Full time
Job Summary

Azzur Group is a GxP compliance and consulting organization dedicated to delivering high-quality, expertly-backed solutions that drive life science companies to success. We are seeking a skilled Process Validation Specialist to support key clients in pharmaceutical manufacturing.

Key Responsibilities

Perform process and equipment validation activities, including gathering historical data, analyzing data using statistical principles, and writing validation protocols and reports. Author validation plans and assist with the development of specifications for user requirements, functional requirements, design requirements, and cycle development protocols for manufacturing process steps. Leverage statistical tools/software to develop process validation strategies and ensure all qualifications and validations are performed according to regulatory and customer requirements. Lead cross-functional review and implementation/execution of documentation with clients or internal stakeholders. Support Quality by Design on the drugs to be transferred or developed on the site. Support risk assessments and pFMEAs generations. Compare results against acceptance criteria and lead the resolution of deviations. Recommend to QA the release of qualified systems. Validate aseptic process and DS/DP manufacturing process (formulation and mixing studies, filling, buffer/media/process holding times). Review validation packages for completeness and accuracy, GDP, scientific rationale, compliance with validation policies and procedures, and accurate data analysis. Compile, maintain, analyze, and make recommendations for value-generating solutions based on data from multiple sources supporting engineering and validation work. Investigate deviations as needed and execute corrections independently. Define and execute improvement projects and initiatives.

Requirements

BS in Engineering, Science, or equivalent technical degree. Experience in a regulated, manufacturing environment within the biotechnology, pharmaceutical, or medical device industry. Experience in the areas of design documentation (URS, FS, DS, and other engineering specifications) Validation (IQ, OQ, PQ, PV, CV, CSV, etc.), Quality Systems (Change Control, Non-Conformances, Requalification, etc.), and Process Excellence Methodologies (Six-Sigma, Lean, etc.). Excellent written and verbal communication skills; excellent technical writing skills. Strong interpersonal skills and the ability to work in a team environment. Ability to work effectively in a fast-paced multitasking environment. Strong working knowledge of FDA and cGMP regulations and documentation practices. Proficient in Microsoft Word, Excel, PowerPoint. Working for multiple clients throughout the region. Azzur Group is an equal opportunity employer and promotes a diverse culture in our workplace. We believe that promoting diversity plays an important role in developing top-quality talent, fostering greater innovation and creativity, and enhancing our relationships with customers and the communities in which we operate. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status.