Manufacture Technology Manager - Medicine

As Manufacturing Technology Manager, you will be at the forefront of driving smooth technology transfer and operational excellence within one of the region’s most respected pharmaceutical manufacturers.

Job Responsibilities:

• Establish and maintain comprehensive product technology transfer systems and process improvement management frameworks that fully comply with product registration requirements and Good Manufacturing Practice (GMP) regulations.
• Organise and coordinate all aspects of product technology transfer initiatives as well as drive continuous improvements in production processes to enhance efficiency and quality.
• Lead the planning, execution, and oversight of trial production runs for new products while testing and evaluating new manufacturing processes to support innovation.
• Review detailed process regulations, approve critical production records, and assess other technical documentation related to manufacturing operations.
• Evaluate records of deviations, changes, or incidents associated with process technology to ensure compliance with internal standards and external regulatory expectations.
• Develop and uphold robust process verification and cleaning management systems that align with GMP requirements to guarantee product safety and integrity.
• Review and approve process verification plans, cleaning validation protocols, and final reports while supervising the implementation of these activities according to established schemes.
• Coordinate cross-functional teams in executing various verification tasks, conducting risk assessments, implementing Standard Operating Procedures (SOPs), and ensuring alignment with best practices.
• Support superiors by undertaking additional assignments as required to meet organisational objectives.

Requirements:

• Bachelor’s degree or higher in pharmacy, pharmaceutics, pharmaceutical engineering or a closely related discipline is essential for this position.
• Proficiency in both Chinese (Mandarin) and English is required; familiarity with Cantonese would be considered an advantage for effective communication within diverse teams.
• A minimum of eight years’ experience in production or research & development roles within large or reputable pharmaceutical companies is necessary.
• Demonstrated expertise in solid dosage forms as well as semi-solid and liquid process technologies along with comprehensive understanding of technology transfer requirements is highly valued.
• Thorough knowledge of current Good Manufacturing Practice (GMP) guidelines as well as industry standards relating to validation processes is expected.
• Exceptional organisational abilities combined with strong coordination skills are needed to manage complex projects involving multiple stakeholders effectively.
• Excellent written and verbal communication skills in English are vital for preparing technical documentation and liaising with internal teams or external partners.
• Ability to demonstrate resilience under pressure while maintaining attention to detail during periods of high workload is important for success in this role.