Validation and Quality Assurance Consultant - Hamlyn Williams
Are you confident in configuring DeltaV batch recipes in a GMP environment?
Do you have hands-on experience with recipe development and validation in pharma or biotech?
Are you looking for a role where you can make a real impact on critical manufacturing projects?
We are seeking an experienced DeltaV Engineer to join a leading pharmaceutical organisation. The successful candidate will be responsible for configuring and maintaining DeltaV systems, with a particular focus on recipe development and batch configuration in line with GMP standards.
Key Responsibilities
* Develop, configure, and test DeltaV batch recipes (ISA-88).
* Support commissioning, qualification, and validation activities.
* Troubleshoot and optimise automation systems within a GMP environment.
* Collaborate with process, quality, and validation teams to ensure compliance.
* Maintain documentation in line with regulatory requirements (21 CFR Part 11, GAMP5).
Requirements
* Proven experience with Emerson DeltaV in the pharmaceutical or biotech sector.
* Strong understanding of batch processing and recipe management.
* Hands-on experience with GMP, IQ/OQ/PQ, and regulatory compliance.
* Ability to work cross-functionally with engineering, validation, and production teams.
* Degree in Engineering, Automation, or related field preferred.
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