The posting
Our client is a Pharmaceutical Supply Chain Solutions industry. Due to their current expansion plan, they are looking for a Regulatory Affairs Specialist to join their team, in hopes of developing the current high performing team. They are located in West.
Job Responsibilities:
- Manage regulatory licence applications, renewals and maintenance.
- Prepare documents for new product launches and licence submissions.
- Prepare and review product registration dossiers and variations.
- Liaise with regulatory authorities and government agencies on regulatory matters.
- Maintain accurate records of product licences, registrations and regulatory documents.
- Prepare and submit required regulatory reports, records and transactions.
- Work with QA and Operations teams to ensure proper product documentation and traceability.
- Review SOPs, work instructions and procedures to ensure regulatory compliance.
- Support regulatory matters relating to Therapeutic Products, Medical Devices, Controlled Drugs and other regulated products.
- Coordinate with internal teams on registrations, renewals, amendments and regulatory projects.
- Perform other ad-hoc duties as assigned.
Requirements:
- Minimum Degree in Pharmacy with relevant Singapore Pharmacy Board.
- Minimum 3 years of relevant experience in pharmacy practice.
- Familiarity with Singapore regulatory requirements relating to Medical Devices, Controlled Drugs and Poison Licenses.
- Experience in regulatory affairs, product registration or licence management will be an advantage.
- Good understanding of regulatory documentation and submission processes.
Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv.
We regret that only shortlisted candidate will be notified.
Email: [email protected]
Recruitpedia Pte. Ltd.
EA License No. 19C9682
EA Reg. No. R23115553 (Lai Hor Yan)



