PAT Specialist

Organon; Cramlington; Presencial; GBP 40.000 - 60.000; Jornada completa

Descripción de la vacante

Organon is hiring a PAT Specialist to join our manufacturing site in Cramlington, Northumberland. The role is the site’s subject matter expert for Process Analytical Technology, driving technical excellence and robust manufacturing performance within the PTO team and global PAT network.

You will support inline production with NIR spectroscopy and real-time release, lead PAT projects, and assist technology transfer and validation while promoting continuous skills development across the site.

Formación

• Master’s degree in Sciences, Analytical Chemistry, or Chemical Engineering.
• Experience with chemometrics is preferred.
• Experience in international and multidisciplinary environments.
• Knowledge of cGMP and pharmaceutical production technologies is desirable.

Responsabilidades

• Provide PAT support for inline production, including NIR spectroscopy and in-process testing.
• Deliver and implement PAT projects across cross-functional teams.
• Support investigations into PAT issues with root-cause analysis and data interpretation.
• Assist with technology transfer, process validation, and PAT equipment installation/qualification.
• Ensure PAT standards and SOPs compliance, and document reviews.
• Contribute to PAT training sessions for colleagues.

Conocimientos

PAT expertise

Analytical chemistry

cGMP knowledge

Multidisciplinary teamwork

Educación

Master’s degree in Sciences/Analytical Chemistry/Chemical Engineering

Herramientas

NIR spectroscopy

Chemometrics

Descripción del empleo

Job Description

Organon is hiring a PAT Specialist to join our world class manufacturing site in Cramlington, Northumberland. As the site’s subject matter expert for Process Analytical Technology (PAT), the PAT Specialist plays a key role in driving technical excellence, innovation, and robust manufacturing performance. Working within the Pharmaceutical Technical Operations (PTO) team and in partnership with the global PAT network, this role ensures the effective generation, validation, and stewardship of digital process data, control strategies, and PAT measurement models.

Collaborating closely with colleagues across Operations, Quality, and Technical functions, the PAT Specialist delivers comprehensive expertise for both drug substance and drug product. They lead and support PAT projects to enable safe, compliant, and timely delivery, while promoting continuous skills development across the site.

The role is actively involved in process development, investigations, and problem-solving activities, as well as facilitating Technology Transfer and Validation for new and existing processes. Responsibilities also include training colleagues in PAT methodologies and supporting the specification, design, installation, and commissioning of new equipment.

Role 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 foundational PAT knowledge.
• Represent the site in global PAT forums, sharing best practice and supporting strategic initiatives.
• Drive continuous improvement by enhancing process robustness, supporting Quality Risk Management, and ensuring all PAT activities meet Safety, Health, Environmental, and Financial requirements.

Skills, Qualifications & Experience

• Master’s degree in Sciences, Analytical Chemistry, or Chemical Engineering required with applicable experience.
• Working knowledge of chemometrics methodologies is strongly preferred.
• Must be highly flexible and possesses relevant experience in working in an international and multidisciplinary environment and able to support the needs of reliable production and supply.
• Working knowledge of current Good Manufacturing Practices (cGMP) preferred and pharmaceutical production and development technologies.

Secondary Job Description

Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women’s Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions. Our Vision is clear: A better and healthier every day for every woman.

Who We Are

As an equal opportunity employer, we welcome applications from candidates with a diverse background. We are committed to creating an inclusive environment for all our applicants.

Search Firm Representatives Please Read Carefully

Organon LLC, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status

Regular

Relocation

Domestic

Travel Requirements

Organon employees must be able to satisfy all applicable travel and credentialing requirements, including associated vaccination prerequisites.

Number Of Openings

1