Pharma/Med Device Validation Engineer (IQ/OQ/PQ Lead)

DIGIDENT LTD; Oxford; On-site; GBP 42,000 - 60,000; Full time

Job summary

DIGIDENT LTD is seeking a Validation Engineer in the Pharmaceutical/Medical Device sector to execute protocols ensuring manufacturing and cleaning processes maintain consistent quality. The role involves performing engineering studies to evaluate new products, new machine validations, change-control assessments, and coordinating computer and method validations of applicable products.

Responsibilities include coordinating projects with vendors, developing timelines, leading IQ/OQ/PQ protocol

Qualifications

• Experience in pharmaceutical or medical device validation.
• Familiar with IQ/OQ/PQ protocols and reporting.
• Strong data analysis and trend interpretation skills.

Responsibilities

• Coordinate validation and installation projects with vendors and service providers.
• Develop and manage project timelines, updating management on progress.
• Lead the writing and execution of IQ/OQ/PQ protocols.
• Compile validation data, prepare reports, and suggest changes or improvements.

Skills

Validation engineering

Quality systems

Equipment qualification

Data analysis

Job description

DIGIDENT LTD is seeking a Validation Engineer in the Pharmaceutical/Medical Device sector to execute protocols ensuring manufacturing and cleaning processes maintain consistent quality. The role involves performing engineering studies to evaluate new products, new machine validations, change-control assessments, and coordinating computer and method validations of applicable products.

Responsibilities include coordinating projects with vendors, developing timelines, leading IQ/OQ/PQ protocol