QA Validation Engineer

CEVA Logistics; Lenexa (KS); Hybrid; USD 75,000 - 95,000; Full time

Job summary

A global logistics company is seeking a QA Validation Engineer in Lenexa, KS. The successful candidate will lead validation activities for processes and systems in the manufacture of regulated veterinary vaccines. Responsibilities include preparing and executing qualification protocols, conducting risk assessments, and ensuring compliance with local and federal regulations. Ideal candidates should have a Bachelor's degree in a related field with substantial validation experience in a GMP-regulated industry. This role does not require travel.

Qualifications

• 4+ years of validation experience in a biotech or GMP-regulated industry.
• 2+ years of validation experience with a Master's degree in related fields.

Responsibilities

• Lead, design, perform, and report on validation activities.
• Prepare and execute various qualification protocols.
• Conduct risk assessments and maintain compliance with regulations.

Job description

QA Validation Engineer

Location: Lenexa, KS

Job Summary and Purpose

The QA Validation Engineer in Lenexa, KS leads, designs, performs, and reports validation activities on processes, equipment, and systems used in the manufacture of regulated veterinary vaccines for domestic and international markets.

Responsibilities and Key Duties

• Prepare and execute protocols including Cycle Development, Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Engineering Studies (ES), Factory Acceptance Test (FAT), and Site Acceptance Test (SAT).
• Review protocol drafts and resolve conflicts or concerns to achieve management pre-approval. Coordinate qualification execution and all aspects of validation projects with Operations, Engineering, Quality Control, and Quality Assurance.
• Perform or supervise protocol execution and maintain documentation in compliance with current Good Documentation Practices (GDP). Review, analyze, and compile protocol data and write reports for management review and approval.
• Perform and document risk assessments to determine validation strategy and approach. Execute re-qualification (RQ) studies and periodic reviews to ensure equipment, systems, and processes remain in a validated state.
• Support and participate in change control processes for qualified and validated equipment, including refrigerators, freezers, incubators, autoclaves, lyophilizers, bioreactors, fermenters, ovens, ampule filling machines, and related systems. Maintain full understanding of applicable change control procedures.
• Provide input to, review, and approve User Requirements Specifications (URS). Write, review, and edit standard operating procedures (SOPs) to align with validation requirements.
• Provide input to Engineering on the preparation and execution of Factory Acceptance Tests (FAT) and Site Acceptance Tests (SAT).
• Research equipment and processes to establish parameters and testing methods that meet validation requirements. Support the development of Validation Plans and Schedules.
• Ensure processes and products comply with all local, state, and federal regulations. Oversee CGMP compliance and establish systems that identify opportunities for improvement and recommend changes to improve process effectiveness and quality.
• Perform all other duties as assigned.

Technical / Functional Competencies

• Ability to perform internal and study audits as a lead and participate in external audits as a member of the audit team.
• Knowledge of pharmaceutical development, regulatory requirements, and manufacturing sciences with a global perspective.
• Knowledge of quality systems tools with the ability to adapt them to organizational needs and global regulatory requirements (GLP, GCP, GMP).
• Ability to validate Excel file programming according to defined objectives.
• Proficiency in the use of data logging equipment and instruments.
• Experience performing risk assessments, investigations, CAPAs, and Aseptic Process Simulations (APS or media fills) preferred.

Education

• Bachelor’s degree in Engineering, Biotechnology, Biology, or Microbiology with 4+ years of validation experience in a biotech, biological, pharmaceutical, or other GMP-regulated industry.
• Masters degree in Engineering, Biotechnology, Biology, or Microbiology with 2+ years of validation experience in a biotech, biological, pharmaceutical, or other GMP-regulated industry.

Physical Requirements

• Ability to read, write legibly, and communicate in English.
• Visual inspection capability.
• Occasional lifting up to 25 pounds.
• Tasks frequently require prolonged mental and visual concentration.

Travel Required

• None.

This job description is intended to convey information essential to understanding the scope, general nature, and level of work performed by job holders. It is not intended to be an exhaustive list of qualifications, skills, duties, responsibilities, or working conditions, nor does it constitute an employment contract. Ceva reserves the right to modify job duties and/or job descriptions at any time to meet business needs.

*VEVRAA Federal Contractor

Ceva is an equal opportunity employer and all qualified applicants will be considered for employment without regard to race, color, religion, sex, national origin, age, genetic information, actual or perceived sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law. Ceva encourages men and women, members of all racial and ethnic groups, individuals with disabilities and veterans to apply.

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