Senior Project Engineer - GMP Biotech Commissioning Lead

PSC Biotech® Corporation; Leinster; On-site; EUR 90,000 - 110,000; Full time

Job summary

PSC Biotech Corporation seeks a Project Engineer to lead cross-functional GMP project delivery for a drug substance and drug product manufacturing facility. You will act as client representative within the Global Engineering Team, coordinating schedules, budgets, start-up activities, and vendor interfaces to meet project objectives.

The role requires a degree in engineering and 8+ years in GMP processing design/start-up environments, with proven project leadership and strong communication

Qualifications

• B.Sc. or M.Sc./M.Eng degree in Engineering (Chemical preferred).
• Experience in Process Engineering.
• 8+ years post- graduate GMP processing design/start-up experience.
• Ability to lead projects.
• Strong teamwork and collaboration skills.
• Excellent communication, presentation, and organizational skills.

Responsibilities

• Preparation of project related deliverables such as schedules, work plans, equipment cost tracking.
• Coordination of project activities between stakeholders.
• Manage installation / start-up / testing of key equipment systems through OQ completion.
• Interface with cross-functional team to ensure systems’ post-OQ (PQ, PPQ) readiness.
• Monitor costs and progress of process suite team milestones with all team members and provide status reports to project Tiers and stakeholders.
• Support cross-functional project teams to ensure project and site stakeholder inputs and requirements are clear and reflected in design deliverables.
• Liaise with stakeholders, equipment vendors, business partners, and SMEs at other sites within the Network as required to support Project.

Skills

Process Engineering

Project lead

Teamwork

Communication

GMP knowledge

Education

B.Sc. Engineering

M.Sc./M.Eng in Engineering

Job description

PSC Biotech Corporation seeks a Project Engineer to lead cross-functional GMP project delivery for a drug substance and drug product manufacturing facility. You will act as client representative within the Global Engineering Team, coordinating schedules, budgets, start-up activities, and vendor interfaces to meet project objectives.

The role requires a degree in engineering and 8+ years in GMP processing design/start-up environments, with proven project leadership and strong communication