Kick-start your regulatory career while getting meaningful exposure beyond "pure RA." In this role, you'll lead day-to-day product registration and quality management system activities, handle HSA correspondence, and also support SOP/product trainings and occasional product presentations to doctors. It's ideal for a junior pharmacist who wants to build strong RA/QMS fundamentals and also explore cross-functional work with Quality, Supply Chain, and Commercial teams.

What you'll do

Regulatory Affairs

• Prepare, submit, and maintain product registration dossiers (new registrations, variations, renewals) via HSA systems; track timelines and respond to authority queries.
• Coordinate labelling/artwork compliance and change controls with internal and external stakeholders.
• Maintain RA trackers, licenses, and product records; ensure documentation is inspection-ready.

Quality & QMS (GDP alignment)

• Support implementation and maintenance of the Quality Management System, including document control, training records, deviations/CAPA, and self-inspections.
• Assist with complaint handling, product returns/recalls, and oversight of suppliers/customers for lawful supply; keep accurate records of delegated duties.
• Partner with logistics/principals to ensure GDP compliance across warehousing and distribution.

Training & Cross-functional Support (additional exposure)

• Coordinate and deliver internal SOP/QMS refreshers and product trainings.
• Prepare materials and occasionally conduct internal product trainings for marketing team as well as product presentations to doctors in collaboration with Medical/Commercial teams (minor but valuable portion of the role).

What you'll bring

• Registered Pharmacist with the Singapore Pharmacy Council (SPC) (required).
• 0-2 years' experience in RA/QMS (fresh graduates welcome); familiarity with HSA guidelines and e-services is a plus.
• Working knowledge or interest in GDP, QMS, CAPA, pharmacovigilance, and inspection readiness.
• Clear, professional communication; strong organization and follow-through across multiple stakeholders.
• Comfort presenting scientific/product content to internal teams and HCPs (training provided).

What you'll gain

• End-to-end exposure across Regulatory Affairs + Quality, with hands-on training and mentorship.
• Cross-functional experience (Medical, Supply Chain, Commercial) and the opportunity to build a well-rounded pharma skill set early in your career.