Quality Assurance Intern

Location: City of Singapore, hirify.global Jurong

Company

hirify.global develops medicines and healthcare solutions, with this role supporting quality operations at the Jurong site.

What you will do

• Support the creation, revision, obsolescence, and overall lifecycle management of GMP documentation.
• Maintain quality agreements and technical specifications with third parties.
• Support internal audits, FDA and HSA regulatory inspections, and site inspection-readiness activities.
• Draft and update procedures, generate compliance reports, and monitor monthly KPIs.
• Collaborate with cross-functional teams and subject-matter experts to ensure documentation meets business, regulatory, and company requirements.
• Support documentation simplification, harmonization, and digitalization initiatives, as well as GEMBA walk-down follow-up actions.

Requirements

• Interest in quality assurance and GMP documentation within site operations.
• Ability to ensure documentation accuracy, completeness, clarity, grammar, and compliance.
• Ability to collaborate with multiple departments and collect, prioritize, and manage documentation changes.
• Willingness to comply with HSE guidelines, Life Saving Rules, and Zero Incident Mindset principles.

Culture & Benefits

• Full-time employment at the hirify.global Jurong site.
• Equal-opportunity workplace supporting diversity and inclusion.
• Exposure to global documentation initiatives and regulated pharmaceutical quality operations.