DeltaV Automation Engineer
Job Description The DeltaV Automation Engineer supports a major capital investment program for a global pharmaceutical leader. In this role, you drive the full lifecycle of biologics manufacturing, from initial development to commercial production. You are responsible for the design, implementation, and integration of Emerson DeltaV control systems. Consequently, you ensure that automation architecture remains […]
Senior QA Specialist
Job Description The Senior QA Specialist drives site quality operations within a GMP-regulated pharmaceutical environment. This role maintains rigorous quality oversight across all site activities, ensuring total compliance with regulatory requirements. You work alongside Manufacturing, Engineering, and Technical Operations to guarantee that site processes, documentation, and quality systems exceed internal and global standards. Key Responsibilities […]
Cost Controller
Job Description The Cost Controller drives financial planning, cost monitoring, and reporting for pharmaceutical manufacturing and capital projects. This position ensures project expenditures track accurately, budgets remain under control, and financial performance aligns with project objectives within a regulated GMP environment. With 2–3 years of experience, you bridge the gap between engineering execution and corporate […]
Project Automation Area Lead
Job Description The Project Automation Area Lead takes technical ownership of control systems within a specific program area of a state-of-the-art multi-product site. You are responsible for shaping the automation architecture, defining ISA-88 structures, and managing system integrators. Your goal is to ensure that complex software deliverables are compliant, consistent, and integrated seamlessly with the […]
Senior Automation Engineer
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Project Manager
Job Description The Project Manager drives the delivery of high-impact manufacturing projects within a global pharmaceutical production environment. In this role, you lead the execution of capital projects ranging from €0.5M to €40M within Manufacturing Operations. You ensure that every initiative hits its milestones on schedule and stays within budget while you maintain the highest […]
QA CSV Engineer
Job Description The QA CSV Engineer provides critical quality oversight for Computer System Validation (CSV) activities within a regulated pharmaceutical environment. In this role, you drive compliance with cGMP, GAMP 5, and global industry standards while managing the validation of complex systems for high-priority projects. You ensure that every stage of the system lifecycle upholds […]
Senior Operations Engineer
Job Description The Senior Operations Engineer drives technical excellence and operational readiness for the GSK HPV project within a high-stakes biologics manufacturing environment. In this role, you provide the critical expertise needed to transition systems from commissioning through to Process Performance Qualification (PPQ). You take ownership of batch record design, recipe optimization, and the seamless […]
EFU Validation Engineer – C&Q
Singapore Job Description The EFU Validation Engineer drives the Commissioning and Qualification (C&Q) lifecycle for Equipment Fan Units (EFU) within a high-stakes regulated environment. In this role, you provide critical technical oversight by managing the end-to-end documentation process, from initial authoring to final approval. You ensure that all EFU systems meet stringent performance standards and […]
Computer System Validation (CSV) Engineer
Singapore Job Description The CSV Engineer supports validation activities for computerized systems used in a regulated pharmaceutical manufacturing and quality environment. This role is responsible for authoring, reviewing, and approving CSV documentation to ensure systems comply with FDA and global requirements, support data integrity, and remain inspection ready throughout the system lifecycle. Key Responsibilities Author […]