Job Description
Our client is seeking an experienced Process Engineer to provide key support and leadership in managing project workstreams, ensuring the successful delivery of site capital projects. This role will focus primarily on a large-scale capacity expansion project involving the construction of a high-volume oral solid dose (OSD) manufacturing facility. Responsibilities Always comply with Health, Safety, and Environmental policies, procedures, and legislation. Ensure all work meets company policies, cGMP, SOP, and regulatory standards. Take ownership of quality compliance in engineering activities. Oversee equipment qualification and process validation for quality compliance. Support project charters, scope definition, and schedule management. Plan, execute, and document project schedules, training, and handover. Coordinate external contractors and liaise with internal departments to meet project deadlines. Draft and review validation documents (SOPs, protocols, reports). Investigate deviations and apply structured problem-solving to resolve project issues. Manage contractor budgets, approvals, schedules, and compliance with site procedures. Build relationships with contractors and ensure their adherence to site requirements. Provide regular updates on schedule, cost, scope, and risks. Prefered Skills/Qualifications You are qualified to a minimum degree level or equivalent in an Engineering discipline 3-6 years of engineering experience working in an oral solid dose pharmaceutical manufacturing (or comparable) environment. Previous project management experience and/or qualification is a distinct advantage For a confidential discussionandmore information on the role,please contactKevin Griffin Kevin Griffin Skills: Engineering Project Management Validation