Regulatory Affairs Specialist – Pharma & Veterinary

Range Pharma Sdn. Bhd.

Petaling Jaya

On-site

MYR 56,000 - 100,000

Full time

14 days+
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Benefits offered by this job

Medical
Miscellaneous allowance
Annual company events
Annual performance bonus

Job summary

Range Pharma Sdn. Bhd. in Malaysia is seeking a Regulatory Affairs professional to handle registration and renewals for local and overseas authorities. You will compile dossiers, respond to queries, and ensure our products stay compliant and market-ready.

The ideal candidate has a degree in Pharmacy or related field and 1–3 years in regulatory affairs. Experience with GMP and vaccines is a bonus. Strong attention to detail and documentation discipline are essential.

Qualifications

  • Degree in Pharmacy, Pharmaceutical Science, Chemistry, Biology, Science, or related field.
  • 1–3 years in regulatory affairs
  • Open to candidates from medical device, food, or supplement registration
  • Bonus: DVS registration, biologics, or vaccines

Responsibilities

  • Prepare, compile, and submit registration and renewal dossiers to local and overseas authorities
  • Follow up on registration correspondence and respond to authority queries
  • Coordinate packaging and marketing materials for compliance and accuracy
  • Liaise with authorities, suppliers, and internal teams on regulatory matters
  • Apply for GMP, CPP, and Certificate of Free Sale as needed
  • Keep the regulatory archive up-to-date and stay current on regulations

Skills

Attention to detail
Regulatory documentation
Cross-functional collaboration
Critical thinking

Education

Bachelor's degree in Pharmacy or related field

Job description

Range Pharma Sdn. Bhd. in Malaysia is seeking a Regulatory Affairs professional to handle registration and renewals for local and overseas authorities. You will compile dossiers, respond to queries, and ensure our products stay compliant and market-ready.

The ideal candidate has a degree in Pharmacy or related field and 1–3 years in regulatory affairs. Experience with GMP and vaccines is a bonus. Strong attention to detail and documentation discipline are essential.

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