Manufacture Technology Manager
7 days ago
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. Job Details Contract Type: Permanent Specialism: Procurement & Supply Chain Focus: Operations Salary: x 12 Months + Bonus Workplace Type: On-site Experience Level: Mid Management Location: Hong Kong Language: Chinese - Bilingual Second Language: English - Bilingual Job Reference: RJUM6K-BC2B5D6A Date posted: 20 October 2025 Consultant: Charmaine Tang #J-18808-Ljbffr
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