Job Description

Link, part of the Clinigen Group, is a rapidly growing global specialty pharmaceutical services business with a unique combination of services across the pharmaceutical lifecycle. We currently have over 1,000 employees headquartered in the UK with global offices in the US, UK and EU, Asia Pacific and South Africa. We're growing rapidly and well positioned for an exciting future of continued expansion.To support our growth, we are currently seeking a detailed orientated and collaborative Regulatory Affairs Project Manager to join our expanding team in Asia Pacific. You will be responsible for ensuring the organisation is meeting its regulatory compliance requirements for new product registrations and variations to existing registrations within assigned portfolio and territories. Experience with HSA and NPRA essential. Experience within other SEA markets desirable.Your valuable work will contribute to the success of regulatory submissions to regional health authorities ensuring that all documents meet the highest standards of accuracy, clarity, and compliance.Please note: this role will operate in a hybrid setting (two+ days per week onsite) if you are located nearby to our Shah Alam offices.RequirementsTo be successful for this position, you'll need:

• A tertiary qualification in a science or related field

• 5+ years demonstrated experience in regulatory affairs roles within South East Asia
• Demonstrated experience working with the HSA and NRPA is essential, with exposure working with other regulatory agencies in the Asia Pacific region such as DOH or FDA highly advantageous
• Demonstrated experience with eCTD publishing experience
• Ability to critically evaluate, analyse and clearly communicate technical information
• Team-orientated, with a collaborative approach to the delivery of tasks and projects

• Annual salary review and performance bonus
• 13th month bonus
• Opportunities for ongoing professional development
• Employee Assistance Program
• Paid Parental Leave

Clinigen