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AA Alive Sdn Bhd in Selangor is seeking a Regulatory Executive to help companies obtain certifications for medical devices and health products, from GDPMD to ISO 13485. You will prepare dossiers and manage submissions for audits and product registrations.
Fresh graduates are encouraged to apply as full training is provided, with a clear growth path into regulatory affairs careers within a fast-growing team.
About the role You'll help businesses get the certifications they need to legally sell and distribute medical devices or health products in Malaysia — from GDPMD to Product MDA, to ISO 13485 and beyond. You will prepare the dossier and documents for audits or product registration submissions.
What you'll do
Guide clients step-by-step through GDPMD, ISO 13485, and other certification requirements
Prepare and organise documentation, applications, and submissions
Keep each client's progress on track and follow up to completion
Stay current on MDA, NPRA and regulatory requirements (we'll train you)
What we're looking for
Highly organised and detail-oriented — this role lives and dies by follow-through
Able to juggle several clients and deadlines without dropping the ball
Fresh graduates encouraged to apply — full training provided
A diploma/degree in any field is welcome; science, business, or quality-related backgrounds are a plus, but attitude matters most
What you'll get
Base salary + commission on KPI hit
Full training in a specialised, in-demand skill set
Clear growth into a recognised regulatory affairs career
A supportive, fast-growing team where your ideas are heard
Your application will include the following questions:
AA Alive Sdn Bhd market and distribute medical devices and consumer health items. Established in 2016, we adopt a customer-first and great after-sales service approach. Underlying this approach are upstanding associates within our organization. As such, we are actively looking for aspiring candidates to accelerate our growth.
What can I earn as a Regulatory Affairs Executive