PAT Specialist: Real-Time Process Analytics & Innovation

Organon LLC; Cramlington; On-site; GBP 70,000 - 90,000; Full time

Job summary

Organon LLC is hiring a PAT Specialist to join our manufacturing site in Cramlington, Northumberland. You will act as the site’s PAT subject matter expert, driving technical excellence, validation, and data stewardship for digital process data and PAT models across drug substance and product.

You will lead PAT projects, support technology transfer and process validation, and train colleagues in PAT methodologies while ensuring compliance with cGMP and safety standards.

Qualifications

• Master’s degree in Sciences, Analytical Chemistry, or Chemical Engineering required.
• Working knowledge of chemometrics methodologies strongly preferred.
• Experience in international and multidisciplinary environments; cGMP knowledge preferred in pharma production and development.

Responsibilities

• Provide PAT support for inline production, including NIR spectroscopy, in-process testing, and real-time release.
• Deliver and implement PAT projects across cross-functional teams, including PoC activities with internal and external partners.
• Support investigations into PAT-related issues, performing root-cause analysis and contributing to statistical and multivariate data analysis.
• Assist with technology transfer, process validation, and the specification, installation, and qualification of PAT equipment.
• Ensure compliance with PAT standards, policies, and SOPs, preparing and reviewing required documentation.
• Contribute to training by delivering PAT learning sessions and supporting colleagues in developing PAT knowledge.

Skills

Chemometrics

Education

Master’s degree in Sciences, Analytical Chemistry, or Chemical Engineering

Job description

Organon LLC is hiring a PAT Specialist to join our manufacturing site in Cramlington, Northumberland. You will act as the site’s PAT subject matter expert, driving technical excellence, validation, and data stewardship for digital process data and PAT models across drug substance and product.

You will lead PAT projects, support technology transfer and process validation, and train colleagues in PAT methodologies while ensuring compliance with cGMP and safety standards.