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 […]
Quality Engineers
Job Description The Quality Engineer ensures that all products, processes, and systems meet rigorous internal standards and external regulatory requirements. In this role, you drive continuous improvement through data-driven analysis, manage the lifecycle of non-conformances, and act as the technical lead for quality assurance during the manufacturing or construction phase. You are the primary advocate […]
C&Q Engineer
Job Description The DeltaV C&Q Engineer is responsible for the commissioning and qualification of Emerson DeltaV software and hardware within GxP-regulated environments. You will lead the transition from code development to operational readiness by executing rigorous testing protocols (IQ/OQ/PQ) and ensuring 100% compliance with ISA-88 standards and site validation master plans. Key Responsibilities Protocol Execution: […]
Senior Automation Engineer
To optimize this role for recruitment platforms and Applicant Tracking Systems (ATS), here are the recommended SEO and structural elements based on the content of the DeltaV Engineer role for the HBV project. Recommended Strategy Element Recommendation Recommended Job Title To optimize this role for recruitment platforms and Applicant Tracking Systems (ATS), here are the […]
QC Analyst
Job Description The QC Analyst executes essential laboratory tasks within the Quality Control department to support pharmaceutical manufacturing. In this role, you take ownership of the analytical testing and documentation for APIs, drug substances, and finished products, ensuring every action meets strict cGxP regulations. You manage the full lifecycle of laboratory activities—from sample storage to […]
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 […]