Regulatory Affairs Specialist - Drive Global Submissions

Boehringer Ingelheim; Kuala Lumpur; On-site; MYR 70,000 - 95,000; Full time

Job summary

A leading global pharmaceutical company in Kuala Lumpur is seeking a Regulatory Affairs Manager to oversee product registrations and ensure compliance with regulations. The ideal candidate should have a degree in Pharmacy or Life Sciences and 2-5 years of relevant experience. Responsibilities include managing regulatory submissions, providing consultation, and maintaining a regulatory database. This role is pivotal for driving healthcare innovation and collaboration across teams.

Qualifications

• 2-5 years of experience in pharmaceutical, medical device, or healthcare industry.
• Good knowledge of national drug regulations and procedures.
• Meticulous attention to detail.

Responsibilities

• Manage regulatory tasks and maintain product licenses.
• Compile registration applications and ensure timely approvals.
• Communicate with regulatory authorities on compliance issues.

Skills

Regulatory compliance

Strong communication skills

Analytical mindset

Computer literacy

Education

Degree in Pharmacy or Life Sciences

Tools

Q3+

Prism

Job description

A leading global pharmaceutical company in Kuala Lumpur is seeking a Regulatory Affairs Manager to oversee product registrations and ensure compliance with regulations. The ideal candidate should have a degree in Pharmacy or Life Sciences and 2-5 years of relevant experience. Responsibilities include managing regulatory submissions, providing consultation, and maintaining a regulatory database. This role is pivotal for driving healthcare innovation and collaboration across teams.