Senior Validation Scientist

Mission Pharmacal; Boerne (TX); On-site; USD 90,000 - 120,000; Full time

Job summary

Mission Pharmacal in Boerne, TX is seeking a Validation Specialist to support equipment qualifications, process validations, cleaning validations, and computerized system validations.

You will prepare IQ/OQ/PQ protocols, gather data from multiple departments, and generate detailed validation reports. The role requires strong problem solving, documentation skills, and collaboration with QA/QC and production teams.

Qualifications

• Bachelor’s degree in engineering, chemistry, or applied science; three years of relevant pharmaceutical/manufacturing experience.
• Ability to demonstrate knowledge across multiple validation categories.
• Strong documentation, analytical, and problem-solving skills.
• Experience with IQ/OQ/PQ and validation protocols.

Responsibilities

• Prepare IQ, OQ, PQ, and re-qualifications for new or modified equipment and systems.
• Gather information from Production, Mechanical Maintenance, and QA/QC to support change control and document reviews.
• Perform routine testing and reporting for utility systems and environmental monitoring.
• Conduct process validations and compile validation study data to meet criteria.
• Prepare, review, and execute CSV validations and SOPs; support software validation activities.
• Coordinate sampling and testing schedules across departments and manage validation reporting.
• Manage cleaning validation studies and determine cleaning limits and hold times.
• Review OOS/OOT results and assist in CAPA and investigations.

Skills

Equipment qualifications

Process validations

Cleaning validations

CSV validation

Validation reporting

QA collaboration

Education

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

Job description

Mission Pharmacal in Boerne, TX is seeking a Validation Specialist to support equipment qualifications, process validations, cleaning validations, and computerized system validations.

You will prepare IQ/OQ/PQ protocols, gather data from multiple departments, and generate detailed validation reports. The role requires strong problem solving, documentation skills, and collaboration with QA/QC and production teams.