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Location
In office (Ireland)
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 8, 2026. First seen by Alion on Nov 6, 2026.

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At PSC Biotech®, we’re more than just consultants — we’re compliance experts. With a global presence and offices spanning across the Americas, UK, Ireland, Europe, Australia, Asia, and the Middle East, we bring local insight with worldwide expertise.
About PSC Biotech Who are we? PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients. 'Take your Career to the next level' PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting. Employee Value Proposition Employees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client’s expectations with regards to quality of all scalable and business unit Role Functions Perform and document testing of raw materials, intermediates, and drug substances in compliance with analytical standards and approved protocols. Provide analytical support for quality investigations, technology transfers, method development, stability programs, and training of laboratory personnel. Principal

Accountabilities Perform testing of raw materials, intermediates, drug substances, and drug products in line with approved methods and specifications. Ensure compliance with cGMP, data integrity, safety, environmental, and company requirements. Accurately document testing activities and maintain laboratory records in electronic systems. Support and lead analytical investigations, including OOS and quality notification activities. Review and verify analytical data and batch documentation prior to product release. Provide analytical support for process changes, technology transfers, product demonstrations, and non-routine testing. Identify, troubleshoot, and resolve analytical and laboratory-related issues. Lead or contribute to continuous improvement, change management, and site initiatives. Serve as a technical resource and subject matter expert for analytical testing and laboratory systems. Train, mentor, and support the development of laboratory analysts and apprentices.

Requirements Technical Knowledge of GMP, quality systems, laboratory safety, and site procedures related to analytical testing and product release. Proficiency in analytical techniques, instrumentation, maintenance, and troubleshooting. Strong understanding of data integrity and ALCOA principles. Business Perform analytical testing with accuracy, precision, and compliance. Maintain complete and accurate laboratory documentation and records. Communicate technical information clearly and effectively. Support projects, audits, investigations, and cross-functional collaboration. Deliver training and knowledge transfer to laboratory personnel. Leadership Demonstrated expertise in analytical chemistry and laboratory operations. Strong technical, problem-solving, communication, and interpersonal skills. Ability to lead initiatives, influence outcomes, and work independently. Educational

Requirements BSc in Chemistry or a related scientific discipline.

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