GMP QA Validation Engineer — Biotech Manufacturing

CEVA SANTE ANIMALE; Lenexa (KS); On-site; USD 70,000 - 90,000; Full time

Job summary

CEVA SANTE ANIMALE is looking for a QA Validation Engineer in Lenexa, KS. The engineer will lead validation activities for veterinary vaccine manufacturing, ensuring compliance with local, state, and federal regulations.

The ideal candidate will have a Bachelor’s degree in a relevant field with 4+ years of experience in validation within a GMP-regulated industry. The role includes reviewing protocols and conducting risk assessments while providing input for quality and compliance initiatives.

Qualifications

• 4+ years of validation experience in a biotech or GMP-regulated industry.
• 2+ years validation experience with a Master’s degree.
• Ability to read, write, and communicate in English.

Responsibilities

• Prepare and execute qualification protocols.
• Perform risk assessments and maintain documentation compliance.
• Support change control processes for validated equipment.

Skills

Internal and study audits

Regulatory requirements knowledge

Quality systems adaptation

Excel validation

Data logging equipment proficiency

Risk assessments experience

Education

Bachelor’s degree in Engineering, Biotechnology, Biology, or Microbiology

Master’s degree with validation experience

Job description

CEVA SANTE ANIMALE is looking for a QA Validation Engineer in Lenexa, KS. The engineer will lead validation activities for veterinary vaccine manufacturing, ensuring compliance with local, state, and federal regulations.

The ideal candidate will have a Bachelor’s degree in a relevant field with 4+ years of experience in validation within a GMP-regulated industry. The role includes reviewing protocols and conducting risk assessments while providing input for quality and compliance initiatives.