Perform biochemical testing and laboratory activities in accordance with approved procedures while complying with GMP/GDP requirements and Quality Control department projects
Prepare laboratory reagents, buffers, and solutions required for testing activities / Adhere to all laboratory and company procedures
Follow and apply all EHS (Environment, Health & Safety) requirements
Complete laboratory forms, logbooks, and documentation in compliance with Good Documentation Practices (GDP), Good Manufacturing Practices (GMP), and ALCOA+ principles
Escalate non-conforming and/or invalid results to the Supervisor on the same day, both verbally and/or in writing, and initiate quality events within required timelines
Conduct laboratory investigations and support deviation management activities / Execute planned activities and proactively communicate any issues impacting deadlines or priorities
Perform qualification protocols for reagents, consumables, and validation activities related to methods, systems, and equipment
Ensure equipment calibration and maintenance are up to date before conducting analyses / Manage Kanban activities in real time
Report procedural deviations and improvement opportunities to Method Owners, Equipment Owners, Supervisors, Delegates, or Subject Matter Experts
Identify and troubleshoot routine technical issues within the scope of expertise / Prepare and/or approve laboratory solutions as required
Maintain laboratory organization and housekeeping according to 5S standards / Support continuous improvement initiatives
Profile
CFC Laboratory Technician, Biology degree, or other relevant scientific qualification
Some years of experience in a Quality Control laboratory within a cGMP-regulated pharmaceutical environment
Experience with laboratory investigations and GMP documentation practices
Strong understanding of quality systems and compliance requirements
Benefits
A highly motivated team and an open way of communication