Validation Scientist: Process Validation & Compliance Expert

Mission-Pharmaca; Mission (TX); On-site; USD 85,000 - 120,000; Full time

Job summary

Mission-Pharmaca in Texas is seeking a technical services professional to support change control, qualification, and validation activities across manufacturing and laboratory operations.

You will prepare IQ/OQ/PQ protocols, perform routine testing, and generate detailed reports. The role requires strong documentation skills and experience with regulatory-compliant qualification and validation processes in pharma environments.

Qualifications

• Bachelor's degree in engineering, chemistry, or applied sciences with 3 years of relevant pharma/manufacturing experience.
• Strong documentation, report writing, and communication skills.
• Experience with qualification, validation, and change control preferred.

Responsibilities

• Prepare IQ/OQ/PQ and re-qualification for equipment and systems.
• Coordinate change control data collection with Production, Mechanical Maintenance, and QA/QC.
• Perform testing and reporting for compressed air systems and air monitoring.
• Execute annual reviews of purified water systems and related validations.
• Conduct qualification process audits to ensure regulatory and internal compliance.
• Prepare validation studies and analyze data to confirm criteria are met.
• Assist with CSV, SOPs, and study design in collaboration with other departments.
• Investigate OOS/OOT results and support CAPA development.

Skills

Pharma validation experience

Documentation

Change control

Education

Bachelor's degree in engineering, chemistry, or applied science

Job description

Mission-Pharmaca in Texas is seeking a technical services professional to support change control, qualification, and validation activities across manufacturing and laboratory operations.

You will prepare IQ/OQ/PQ protocols, perform routine testing, and generate detailed reports. The role requires strong documentation skills and experience with regulatory-compliant qualification and validation processes in pharma environments.