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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