Beranda Loker Detail
M
Pharmaceuticals 🏢 Full Time ⭐️ Terverifikasi

Protege Trainee in Regulatory Affairs

M.S. Ally Pharma
Petaling Jaya, Selangor
Estimasi Gaji
RM 2.000 – RM 2.000
Live Update
12 Juni 2026
Batas Akhir
12 Jun 2027

Deskripsi Pekerjaan

Are you a fresh graduate passionate about the pharmaceutical industry? M.S. Ally Pharma is seeking a motivated Protege Trainee in Regulatory Affairs to launch your career in compliance and regulatory oversight. This full-time training program offers hands-on experience in navigating the complex regulatory landscape of pharmaceutical products, preparing you for a future as a regulatory affairs professional.

As a Protege Trainee, you'll gain exposure to regulatory documentation, submission processes, and compliance standards while developing critical attention to detail and analytical skills. Our mentorship-driven environment provides structured learning opportunities where you'll collaborate with experienced regulatory professionals to understand industry best practices and evolving regulatory requirements.

This position is ideal for recent graduates with a strong academic background in life sciences who thrive in dynamic, detail-oriented settings. Join us to build a solid foundation in regulatory affairs while contributing to our mission of ensuring compliance and quality in pharmaceutical products.

Tanggung Jawab

  • Assist in preparing regulatory documentation for product submissions and approvals
  • Monitor and analyze regulatory changes in pharmaceutical guidelines and requirements
  • Support maintenance of regulatory compliance databases and records
  • Collaborate with cross-functional teams to ensure regulatory alignment
  • Participate in internal audits and compliance assessments
  • Research and summarize regulatory updates for team dissemination
  • Contribute to developing regulatory strategies for new product launches

Kualifikasi

  • Bachelor's degree in Pharmacy, Life Sciences, Chemistry, Biology, or related field
  • Strong attention to detail with excellent organizational skills
  • Eagerness to learn and develop in regulatory affairs domain
  • Excellent written and verbal communication abilities
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
  • Basic understanding of regulatory frameworks (GMP, GLP, etc.)
  • Ability to work independently and collaboratively in team environments

Keahlian yang Dibutuhkan

Regulatory Affairs Compliance Documentation Pharmaceutical Guidelines Research Analysis Communication Microsoft Office GMP GLP

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