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Intern, Regulatory Affairs Operations (PECT)
- Internship, onsite
- Haleon
- Singapore, Singapore
Salary undisclosed
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- Local Regulatory Affairs:
- Understanding of legal and technical requirements for drug registration
- Application of important and relevant international guidance viz. ICH stability requirements, ASEAN technical requirements on stability, process validation and bioequivalence studies
- On-the-job training – submission of new application/variation
- Medical advertisement control
- Global Regulatory Affairs (Intel and Policy):
- Understand Haleon’s Global Regulatory Intel and Policy (GRIP) function, 9-box external engagement framework and external engagement tools & assets (e.g. policy papers, heat map, SWOT and action plan).
- Perform regulatory intelligence monitoring activity (scan, interpret and communicate), including drafting of REGULUS posts
- Participate in Global Regulatory Intelligence Network (GRINs) and Global Regulatory Education Forums (GREFs)
- Quality Assurance:
- Quality oversight in organization (from product inbound receiving up to market distribution)
- Technical Terms of Supply or Quality Assurance Agreement with manufacturing site
- Product Complaint handling / product defect reporting
- Product incident management / Recall execution
- Completion of Year 3 NUS Pharmacy study programme
- Successfully achieve passing grades for all related modules in NUS without any negative track records
- Previous experience in similar industries is a bonus.
- Responsible and Driven attitude
- Ability to collaborate and work with cross functional teams.
- Communications Skills
- Interpret the Health Products Act (from the amalgamation of the Medicines Act, the Poisons Act) and the Medicines (Advertisement & Sale) Act;
- Understand and apply the ASEAN and ICH Common Technical Document format requirements in regulatory submissions;
- Understand, apply and fulfil the Singapore medicinal product, medical device, cosmetic and complementary medicines regulatory requirements in regulatory submissions;
- Understand and apply the artwork development system for the development of printed components;
- Understand and be able to chart regulatory activities that are needed to support source switch/ new product launch
- Understand the Quality System elements expected of a commercial sales and marketing establishment by the Health Sciences Authority (Product Complaint Handling, Product Recall, Good Distribution Practices);
- Understand and apply the process for the development, review and approval of scientific and unbiased promotional materials that facilitate communication with healthcare professionals and the lay public;
- Understand and apply the process to manage enquiries from the public and healthcare professionals.
- Local Regulatory Affairs:
- Understanding of legal and technical requirements for drug registration
- Application of important and relevant international guidance viz. ICH stability requirements, ASEAN technical requirements on stability, process validation and bioequivalence studies
- On-the-job training – submission of new application/variation
- Medical advertisement control
- Global Regulatory Affairs (Intel and Policy):
- Understand Haleon’s Global Regulatory Intel and Policy (GRIP) function, 9-box external engagement framework and external engagement tools & assets (e.g. policy papers, heat map, SWOT and action plan).
- Perform regulatory intelligence monitoring activity (scan, interpret and communicate), including drafting of REGULUS posts
- Participate in Global Regulatory Intelligence Network (GRINs) and Global Regulatory Education Forums (GREFs)
- Quality Assurance:
- Quality oversight in organization (from product inbound receiving up to market distribution)
- Technical Terms of Supply or Quality Assurance Agreement with manufacturing site
- Product Complaint handling / product defect reporting
- Product incident management / Recall execution
- Completion of Year 3 NUS Pharmacy study programme
- Successfully achieve passing grades for all related modules in NUS without any negative track records
- Previous experience in similar industries is a bonus.
- Responsible and Driven attitude
- Ability to collaborate and work with cross functional teams.
- Communications Skills
- Interpret the Health Products Act (from the amalgamation of the Medicines Act, the Poisons Act) and the Medicines (Advertisement & Sale) Act;
- Understand and apply the ASEAN and ICH Common Technical Document format requirements in regulatory submissions;
- Understand, apply and fulfil the Singapore medicinal product, medical device, cosmetic and complementary medicines regulatory requirements in regulatory submissions;
- Understand and apply the artwork development system for the development of printed components;
- Understand and be able to chart regulatory activities that are needed to support source switch/ new product launch
- Understand the Quality System elements expected of a commercial sales and marketing establishment by the Health Sciences Authority (Product Complaint Handling, Product Recall, Good Distribution Practices);
- Understand and apply the process for the development, review and approval of scientific and unbiased promotional materials that facilitate communication with healthcare professionals and the lay public;
- Understand and apply the process to manage enquiries from the public and healthcare professionals.