Architecture & Pipeline: Design and govern data model (Medallion architecture) and oversee the implementation (e.g. data lakes, build automated batch / real-time streaming pipelines, data source integrations)
Design, build, and optimize scalable pipelines for ingesting, transforming, and integrating large-volume datasets (market data, news feeds and various unstructured data sources).
Position: CIP Engineer (Clean-in-Place) - Engineering & CQV Location: Singapore The CIP Engineer will be responsible for the design review, commissioning, qualification, validation, optimization, and lifecycle management of Clean-in-Place (CIP) systems within pharmaceutical, biopharmaceutical, vaccine, API, and sterile manufacturing facilities. The role requires a combination of engineering expertise and CQV experience to ensure that CIP systems are designed, installed, tested, and operated in compliance with cGMP, FDA, EU GMP Annex 1, ISPE, and company quality standards. The successful candidate will support project execution from Concept Design through Operational Qualification (OQ), Performance Qualification (PQ), and Continued Process Verification (CPV) Responsibilities Engineering Responsibilities
Project involvement from initial scoping through detailed design and commissioning and handover across a wide variety of projects, including preparation of technical specifications, reports, and estimates.
Technical Ownership: Lead the end-to-end delivery of complex features, ensuring that technical designs are robust, scalable, and aligned with long-term goals.