• To performs direct installation activities, such as creation, execution and completion of installation records of the clinical studies
• To Perform direct qualification activities, such as creation, execution and completion of qualification protocol (QMP)
• To liaise with external parties on equipment and consumables. This can include quotation request, management of service/maintenance contracts/agreements, repairs and disposal.
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- To be responsible in managing the CER, Compliance Work Bench and related system for Singapore plant.
- Prepare and submit Product Environmental Data to Customers (Internal and External) on time with accuracy.
- To liaise and keep Singapore Plant, Suppliers and Singapore Product Development Team updated on Molex Chemical Substances Specification for Products and Packaging (MCSS).
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Work done will be at the direction of the PI, and where relevant, the Industry Director and Centre Director.As the Programme is interdisciplinary and multidisciplinary by nature, you will be expected to convey yourdomain expertise and edify others (and vice versa) in as productive, constructive, and collaborative a manner as possible.
You may be asked to participate in the development of use cases and delivery of proof-of-concept prototypesfor government and industry partners in the areas of computable contracts and "rules as code". Experience inrequirements analysis and agile, iterative methodologies will be useful at this stage.The work of the team will be largely determined by these use cases and customers. We will work with multipleuse cases so that we can abstract across them and develop generalized, reusable infrastructure. We will workwith specific customers so we can build useful applications on top of that infrastructure.You will contribute to the design and development of open-source software written to serve those use cases.You will work as part of a team of research engineers, developers, and domain expertise and you will beexpected to actively participate in team meetings and text-based communications. You will be expected to beactive members of the applied research community, by validating and contributing to advances incomputational law.
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• To performs direct installation activities, such as creation, execution and completion of installation records of the clinical studies
• To Perform direct qualification activities, such as creation, execution and completion of qualification protocol (QMP)
• To liaise with external parties on equipment and consumables. This can include quotation request, management of service/maintenance contracts/agreements, repairs and disposal.
...