Technical Group Leader; NIGHT SHIFT

Department: B200 Downstream, Upstream, MWS

We currently have multiple positions open for this role, and the start date is in October 2026.

Inclusive from Tuesday‑Saturday or Sunday‑Thursday or Friday to Tuesday from 10:00 p.m. – 06:00 a.m. (Subject to change)

• Schedule and coordinate daily/weekly work of a group of technical staff in B200 as per area requirements.
• Check and review Records, SOP, logbooks/e-logbooks, BPRs/e-BPRs, and monitoring charts for completion and accuracy of all documents as per GMP guidelines.
• Ensure equipment is kept in good GMP condition (with preventive maintenance, validation and calibration)
• Order and ensure adequate chemicals, supplies, and spare parts for equipment
• Train and ensure technical staff comply to GMP and SOP requirements
• Facilitate daily meetings and report findings to management
• Initiate and file deviations and lead investigations
• Coordinate and support units within department (Upstream, Downstream, MWS) and other outside departments (Maintenance, Automation, QO test labs, etc.) and ensure timely completion of production activities.
• Perform other duties as assigned by Department Management throughout all stages of drug substance manufacturing
• Supervise material handling in B200 Shipping, Receiving, and storage areas.

• Coordinate, oversee, and confirm technical staffs completion of SAP activities/transactions
• Capacity planning and scheduling of materials and personnel
• Create work orders for ETS/Maintenance
• Maintain master recipes and production inventory
• Create and maintain process orders with authorization to change orders upon demand
• Ensure all data input is completed accurately and in a timely manner such as investigation data, LIMs, deviation filing, change request forms, etc.
• Perform activities in PCS and review data as required

• Perform and delegate production calculations, measurements and release checks. Ensure each cleaning meets standards set in SOP, records, and in accordance with GMP.
• Observe in detail and report any process deficiencies, perform visual inspection of equipment for impurity and damage before and after cleaning.
• Perform and delegate utility sampling and environmental monitoring as required and ensure completion on schedule
• Train technical staff on problem solving and troubleshooting as required.
• Ensure area is inspection ready. Knowledgeable to guide inspectors

• Train and ensure technical staff comply with HSE requirements
• Ensure operators are equipped and use proper PPE when performing tasks.
• Ensure operations are performed in an ergonomic way and elevate any potential hazards. Help develop proposed solutions.
• Ensure routine HSE checks and inspections are completed in a timely manner.
• Ensure cleaning chemicals and equipment are stored and used as per HSE requirements and have SDS available.

• Coordinate and schedule work of technical staff in facility, equipment, and process improvement projects with Manufacturing Technology (MTech) and facility management (Engineering & Technical Services)
• Write or modify specifications, protocols and reports related to facility, equipment including SOP’s, BPR’s.
• Perform activities involved in IQ, OQ, and PQ for new equipment
• Initiate CCR, CAPA in Quality system as needed and manage them until completion as per committed due dates

• Minimum 3 years College Diploma in Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related Life Sciences field.
• Minimum of three (3) years of relevant work experience.
• Preferred Bachelor’s degree (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related Life Sciences), with a minimum of three (3) years of relevant work experience.
• Proficiency in pharmaceutical manufacturing, protein purification,…