Orion Group
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Expired Jobs
Tuas
- Execute drug product manufacturing operations including dispensing, blending, granulation, compression, coating, and filling
- Operate and perform basic maintenance on pharmaceutical manufacturing equipment
- Complete batch records, logbooks, and GMP documentation accurately and in real-time ...
Posted
a month ago
Singapore
- Orion Group Life Sciences are currently recruiting a Regulatory Affairs Manager on behalf of our Multinational Biopharmaceutical Client based in North Buona Vista Drive, Singapore on an initial 12-month contract with potential to extend.
- The Manager, Regulatory Affairs (RA) serves as the primary JAPAC representative of the regulatory affairs function within both the R&D and commercial organizations for all matters related to assigned therapeutic areas and products. The incumbent is responsible for defining, implementing, and delivering Area and Affiliate regulatory strategies across a portfolio of compounds in late-stage development and marketed products within the JAPAC region. With knowledge in regional regulatory requirements, the role acts as a subject matter expert for assigned countries, continuously monitoring and interpreting regulatory policy and intelligence relevant to those markets. In addition, the incumbent represents the RA function in cross-functional initiatives being led out of the Area office.
- Major Responsibilities: ...
Posted
a month ago
Tuas
- Execute drug product manufacturing operations including dispensing, blending, granulation, compression, coating, and filling
- Operate and perform basic maintenance on pharmaceutical manufacturing equipment
- Complete batch records, logbooks, and GMP documentation accurately and in real-time ...
Posted
2 months ago
Tuas
- Execute upstream and/or downstream and/or central service biomanufacturing processes per approved batch records and SOPs
- Operate bioreactors, centrifuges, buffer, chromatography systems, or other related bioprocess equipment
- Perform in-process sampling, testing, and monitoring of critical quality attributes ...
Posted
2 months ago
Tuas
- Administer the document management system (DMS) for SOPs, batch records, protocols, and reports
- Process document initiation, revision, review, approval, and distribution workflows
- Ensure document version control, archiving, and retrieval processes comply with GMP and GDocP standards ...
Posted
2 months ago