Contract Validation Engineer

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

Our Client is seeking a validation engineer within the Pharmaceutical / Medical Device sector to execute protocols to demonstrate that manufacturing and cleaning processes are carried out with consistent quality.

As a validation engineer you will also be performing engineering studies to evaluate new products or components, new machine validations, change control assessments, and coordination of computer and method validations of applicable products.

Responsibilities:

• Coordinate projects directly with vendors and service providers to ensure that all validation and installation requirements are being satisfied during the execution of protocols.
• Develop timelines for all projects and ensure that deadlines and goals are being met. Frequently update management and team on progress.
• Being the lead on the writing and execution of IQ/OQ/PQ protocols.
• Compile and analyse validation data, prepare reports, and make recommendations for changes and/or improvements.