Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Did you know that we are the 1st biologics contract manufacturer in Singapore? We offer you exposure to upcoming biotech and established pharmaceutical companies and to the manufacturing technology needed to produce mammalian treatments and cell therapies of tomorrow. Our global manufacturing network is recognized for its reliable, high-quality services, regulatory track record, global footprint, innovative technology platforms and extensive experience – we, in Singapore are proud to be part of this global network.
As an Associate Director of Technology/Method Transfer, you will be responsible for managing day-to-day activities in a GMP biotech contract manufacturing facility, ensuring compliance with approved SOPs and policies across multiple products. You will lead and oversee method transfer, validation, and lab studies while supervising or developing staff. The role involves providing critical support for customer projects, managing resources, and ensuring coordination across functions.
Key Responsibilities:
- Oversee laboratory activities such as assay transfers, disinfection studies, stability programs, equipment validation, and cleaning validation.
- Ensure the collection, management, and dissemination of project-related information to clients and internal teams.
- Coordinate project communications, reporting, and administrative tasks.
- Provide stakeholders with key data and updates on project status, including timelines, budgets, resources, and any delays.
- Ensure projects are completed within the approved budget, including resource planning, cost estimating, budgeting, and cost control.
- Act as a liaison between clients, QC, QA, and management, coordinating project plans, execution, and change controls.
- Manage cross-functional operational integration for project teams.
- Engage within the Lonza Global Network, building industry expertise both internally and externally.
- Apply advanced industry knowledge to make decisions autonomously.
- Communicate quality operations and compliance updates to senior management effectively.
- Review and approve SOP protocols, reports, and records.
- Lead or supervise staff in investigations, change control, CAPA proposals, and discrepancy report closures.
- Participate in global harmonization and efficiency projects.
- Support departmental budget control and capital expenditure management.
- Mentor, coach, and develop high-performing individuals and teams, ensuring succession planning for key roles.
- Contribute to organizational change and continuous improvement efforts.
Key Requirements:
- Degree or higher in Life Sciences/Pharmaceuticals with extensive experience in supervisory/project management roles within QC/QA.
- 10+ years of experience in quality or manufacturing operations in a GMP, FDA, and EU-regulated pharmaceutical environment.
- In-depth knowledge of regulatory requirements, including FDA and EMEA guidelines.
- Strong expertise in validation programs within GMP facilities.
- Demonstrated ability to set clear goals, prioritize tasks, and make balanced decisions to meet deadlines.
- A team player with a focus on safety, quality, and timelines.
- Lead organizational change.
- Excellent conflict resolution skills.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
