Technical LIMS Computer Scientist (cGMP Focus) Consultant Ontario, Toronto, ON, CA 30+ days ago Requisition ID: 1156 PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products. At PharmEng Technology, we strive to cultivate the best working workplace where empowerment, passion and perseverance are nurtured while serving our clients to achieve their unique business goals. We are seeking a highly skilled and technical LIMS Specialist with a strong understanding of cGMP (Good Manufacturing Practices) to join our team in Toronto, Ontario . This role requires an individual who is not only adept in programming and system customization but also has a solid grasp of data governance, data integrity, and compliance within a pharmaceutical or biotech environment. Responsibilities: Act as the LIMS System Owner,
coordinating and overseeing the delivery of system changes and evolutions in partnership with a global team. Manage relationships with internal business customers and related IT development and support teams. Develop, maintain, and modify the analytical testing portfolio through LIMS master data management processes. Data Governance: Build and support the current and updated master data governance model for vaccine product specifications and analytical testing. Foster transparent sharing of scientific and testing data semantics through a common internal reference model. Support the Data Logistics & Support (DLS) Department, ensuring delivery of project and operational objectives. Understand the cGMP requirements for data collection models from testing performed using various QC laboratory instruments, TCU, and related computerized systems. Support the activities related to maintaining all commercial product master specification documents for Industrial Affairs. Ensure that data