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Location
In office (Dublin)
Seniority
Senior
Employment
Contractor

Confirmed on the employer's own hiring board on Nov 3, 2026. First seen by Alion on Nov 3, 2026. QCS Staffing scores A on the Alion truth index.

Overview
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QCS Staffing, formerly Quanta Consultancy Services, is a specialist recruitment agency headquartered in Berkhamsted, Hertfordshire, that places contractors, permanent staff and executives in life sciences, data centres, IT, renewable energy and heavy lift. Founded in 1992, it has worked for clients in more than 30 countries and runs offices in the UK, the United States, Ireland, Puerto Rico and the Netherlands, including one in Research Triangle Park, North Carolina. Its assignments include project, process, CQV and automation engineers, construction and electrical design managers, procurement advisers and network engineers on client capital projects.
Senior Process Engineer Specialist - Dublin, Ireland - Initial 11-Month Contract - Life Sciences Our client is a global leader in pharmaceutical innovation, specialising in the development and manufacture of cutting-edge drugs. As they continue to grow, they’re seeking an experienced Senior Process Engineer Specialist to support their dynamic team and drive forward groundbreaking projects in Dublin. What you’ll deliver:

Support the design, construction, qualification, and startup of upstream and downstream biologics manufacturing equipment.Support technology transfer and commercialisation activities for biologics manufacturing processes.Monitor process performance using CPV, SPC, MVDA, and PAT methodologies to identify trends and drive improvements.Support process investigations, deviations, change controls, process validation, and continuous improvement initiatives.

What you’ll need:

Extensive experience (MSc) or (BSc) experience within biotechnology, pharmaceutical manufacturing, process engineering, MSAT, or technical operations.Strong understanding of biologics manufacturing processes, including upstream cell culture and/or downstream purification.Extensive knowledge of GMP regulations, process validation, quality systems, deviation management, and change control.Experience with process monitoring tools such as CPV, SPC, MVDA, PAT, and statistical analysis software including JMP or Design Expert.

If this assignment is of interest to you, please apply now! #LI-CH3

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