Onsite Validation Analyst I — QA & Compliance

Kansas City Zone; Kansas City (MO); Hybrid; USD 65,000 - 85,000; Full time

Benefits offered by this job

Medical, dental, vision benefits

Tuition reimbursement

Paid time off & holidays

Job summary

Catalent’s Kansas City facility is seeking a Validation Analyst I to support validation programs across manufacturing and laboratory disciplines. The role ensures compliance with Catalent guidelines and regulatory requirements while managing validation deliverables.

100% onsite in Kansas City, MO, with a Monday–Friday 8am–5pm shift. The candidate will collaborate with site IT, Global IT, QA, and multiple business units to drive successful validation outcomes and contribute to continuous

Qualifications

• Bachelor's degree in Life Sciences, Engineering, or related field.
• Minimum of 2 years of validation, engineering, or related experience.
• Strong and in-depth knowledge of validation, quality, and regulatory compliance.
• Understanding of pharmaceutical solid dose manufacturing and analytical testing.
• Familiarity with cGMP, ISPE GAMP5, and FDA/MHRA requirements.
• Clear verbal and written communication skills.

Responsibilities

• Ensure validation deliverables are executed per objectives, timelines, and quality requirements.
• Generate, execute (where applicable), approve, and summarize validation protocols for equipment qualification and commissioning.
• Collaborate with external vendors, IT, Validation, QA, and manufacturing units to manage validation deliverables.
• Apply project management skills for procurement, integration, and implementation of new systems.
• Support continuous improvement initiatives and validation policy development.
• Perform other duties as assigned.

Skills

Validation expertise

Regulatory compliance

Communication

MS Office proficiency

Team collaboration

Education

Bachelor's Degree in Life Sciences/Engineering

Tools

SharePoint

Microsoft Office

Job description

Catalent’s Kansas City facility is seeking a Validation Analyst I to support validation programs across manufacturing and laboratory disciplines. The role ensures compliance with Catalent guidelines and regulatory requirements while managing validation deliverables.

100% onsite in Kansas City, MO, with a Monday–Friday 8am–5pm shift. The candidate will collaborate with site IT, Global IT, QA, and multiple business units to drive successful validation outcomes and contribute to continuous