Validation Analyst I – Onsite: Grow with Pharma

Catalent; Kansas City (MO); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Competitive PTO and holidays

Benefits from day one

Tuition reimbursement

Career growth opportunities

Job summary

Catalent in Kansas City, MO is seeking a Validation Analyst I to support validation programs across manufacturing and laboratory disciplines. You will ensure compliance with Catalent guidelines and regulatory requirements while managing validation deliverables, collaborating with Site IT, QA, and Manufacturing teams.

Shift: Mon to Fri 8am-5pm; Location: Kansas City, MO; 100% Onsite. This role offers exposure to GMP equipment qualification and opportunities to contribute to process improvements

Qualifications

• Bachelor's degree in Life Sciences, Engineering or related field.
• Minimum of 2 years of validation, engineering, or related experience.
• Strong knowledge of validation, quality and regulatory compliance.

Responsibilities

• Ensure validation program deliverables are executed per objectives, timelines, resources and quality.
• Generate, execute, approve and summarize validation protocols for GMP equipment qualification.
• Collaborate with internal teams and vendors to manage validation deliverables.
• Apply project management in procurement, integration and implementation of new laboratory software and instruments.
• Participate in and support continuous improvement initiatives.
• Assist in developing, training, and implementing validation policies and procedures.
• Perform other duties as assigned.

Skills

Validation knowledge

Regulatory compliance

Technical writing

Communication skills

Problem solving

Education

Bachelor's Degree in Life Sciences/Engineering

Tools

Microsoft Office

SharePoint

Job description

Catalent in Kansas City, MO is seeking a Validation Analyst I to support validation programs across manufacturing and laboratory disciplines. You will ensure compliance with Catalent guidelines and regulatory requirements while managing validation deliverables, collaborating with Site IT, QA, and Manufacturing teams.

Shift: Mon to Fri 8am-5pm; Location: Kansas City, MO; 100% Onsite. This role offers exposure to GMP equipment qualification and opportunities to contribute to process improvements