Today, Lonza is a global leader in life sciences operating across five 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.
The Technical Writer is responsible in the development and/ or revision of Master Batch Records (MBRs) and other current Good Manufacturing Practice (cGMP) documents e.g. Standard Operating Procedures (SOPs), Work Instructions (WIs) used in the execution of manufacturing processes and/ or onsite operations.
What you’ll get
An agile career and dynamic working culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
Daily company bus from the MRT location near your home to and from the Tuas site.
Fully paid medical insurance, and option to enrol family members at partially subsidized premiums.
The full list of our global benefits can be also found on https://www.lonza.com/careers/benefits.
What you’ll do
Develop new MBRs and Work instruction (WI), using existing templates, in support of Technology Transfers and revise existing ones ensuring adherence to approved template/ structure
Produce high-quality documentation that meets applicable standards/ requirements of the users
Write and edit technical information/ instructions in a manner to ensure content is factual and accurate.
Collaborate closely with relevant SMEs/ customers on documentation requirements to ensure specialized topics and comments from internal review are appropriately addressed/ discussed 3. Generate Aseptic Process Simulation Summary Report
Manage the lifecycle of MBRs including, but not limited to creation, review, revision and approval on product campaign basis
Maintain a system for tracking changes to be implemented in all upcoming product campaigns
Communicate actively to address customers’ comments and to clarify customers’ queries with respect to MBRs
Deliver MBRs/ WIs with strict adherence to the production schedule
Support change request process:
Provide assessments and insights to Change Requests as needed
Define Change Tasks as needed and close tasks in a timely manner
Close assigned CAPAs in a timely manner
What We’re Looking for
Strong technical communication and writing skills
Effective interaction skills with cross functional teams and customers
Knowledge in Controlled Document Management System (DMS) and Trackwise or similar systems
Ability to quickly grasp and translate complex technical concepts to comprehensible instructional texts
Ability to influence peers and teams with no direct reporting lines
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.