Process Engineer TPM5972

Tandem Project Management Ltd.; Cork; Hybrid; EUR 70,000 - 100,000; Full time

Job summary

Tandem Project Management Ltd. seeks a Process Design Engineer to join our life sciences team. You will develop PFDs, P&IDs, mass balances, equipment lists, and design documentation across pharma, biotech, and life sciences projects.

You will lead process safety activities (HAZOP, ATEX), contribute to C&Q, support automation, coordinate with internal and external teams, and review vendor submittals to ensure GMP-compliant designs.

Qualifications

• Bachelor’s degree in Chemical/Process Engineering; Master’s or chartership desirable.
• 3–8+ years’ experience in process design within regulated industries (pharma, biotech, life sciences).
• Proven ability to develop PFDs, P&IDs, mass balances and perform sizing calculations; GMP experience.

Responsibilities

• Develop process deliverables (PFDs, P&IDs, mass balances) for design packages.
• Prepare technical datasheets and specifications for procured equipment.
• Lead HAZOP studies, ATEX assessments and process safety activities.
• Coordinate design activities with internal teams, sub-consultants, vendors and contractors.
• Review vendor/subcontractor submittals for compliance with project requirements.
• Support commissioning, FATs and C&Q activities and site visits.

Skills

Process design

PFDs & P&IDs

HAZOP

ATEX

GMP

Cross-disciplinary collaboration

Technical documentation

Education

Bachelor's degree in Chemical/Process Engineering

Master’s degree or chartership desirable

Job description

Summary:

We are looking for a Process Design Engineer to join our growing team who will be involved in the preparation of project scope statements, design brief and User Requirement Specifications on numerous projects in the life sciences sector.

Responsibilities:

• Develop process deliverables including PFDs, P&IDs, and mass balances to support project design and execution.
• Generate and maintain equipment lists, line lists, and associated design documentation.
• Perform process calculations for utility systems, equipment sizing, vessels, and in-line instrumentation.
• Prepare technical datasheets and specifications for the procurement of process equipment.
• Compile comprehensive design packages for tender and IFC (Issued for Construction), including calculations, datasheets, specifications, scopes of work, and tender documentation.
• Develop and document process design philosophies and engineering standards.
• Lead and participate in process safety activities such as HAZOP studies, ATEX assessments, and design risk assessments.
• Collaborate with multidisciplinary teams to ensure integration and alignment across all engineering disciplines.
• Support and contribute to automation and control system design.
• Coordinate design activities between internal teams, sub-consultants, vendors, and contractors to ensure timely and accurate project delivery.
• Review and respond to technical queries from contractors and vendors.
• Review and approve vendor and contractor submittals to ensure compliance with project requirements.
• Participate in Factory Acceptance Tests (FATs) for process equipment as required.
• Support construction activities through site visits, technical query resolution, and quality checks.
• Prepare and deliver client presentations; actively participate in client meetings.
• Stay current with developments in the life sciences sector, identifying opportunities for innovation and business growth.
• Support commissioning and qualification (C&Q) activities, including preparation, approval, and execution of protocols in collaboration with sub-consultants.
• Ensure compliance with company procedures, client site rules, and SOPs at all times.

Qualifications & Experience:

• Degree qualified in process engineering or related discipline. Bachelor’s degree in Chemical/Process Engineering (Master’s or chartership with Engineers Ireland or equivalent desirable).
• 3 to 8+ years’ experience in process design within regulated industries (pharma, biotech, or life sciences).
• Proven ability to develop core process deliverables (PFDs, P&IDs, mass balances) and perform equipment/utility sizing calculations.
• Experience with GMP environments and participation in safety reviews (e.g. HAZOP, ATEX, risk assessments).
• Strong track record of working with multidisciplinary teams, vendors, and contractors across full project lifecycles, including FATs and C&Q support.