Senior Regulatory Affairs Manager | FMCG

Job Title: Senior Regulatory Affairs Manager | FMCG
Contract Type: Permanent
Location: Bangkok, Thailand
Salary: Negotiable
Start Date: ASAP
Reference: 4a8bd3b8f1f7281c83df_1502877279
Contact Name: Withida (Dow) Marlow
Contact Email:
Job Published: August 16, 2017 16:54

Job Description

Role Overview

The Senior Regulatory Affairs Manager will lead and manage all regulatory and quality systems for three Business Units and ensure fully regulatory compliance in Thailand for this leading consumer products multi-national company.

Key Responsibilities | Deliverables

  • Drive reduction of registration cycle time through Speed to Market initiatives.
  • Work closely with Global RA team to obtain complete registration documents for faster product registrations in Thailand.
  • Understand and influence Thailand regulatory environment by leveraging key relationships with industry groups.
  • Define and implement regulatory strategy and plan for 3 Business Units in Thailand.
  • Assist Commercial team on product artworks and labelling compliance.
  • Support Regional QA in the development and implementation of Quality System in Thailand.
  • Provide leadership in interpretation. Provide support and advice to the parties involved (employees, customers, distributors, suppliers, etc.) to understand and follow the SOP in accordance with Corporate Quality Policy.
  • Provide training to Thailand employees in all RA & QA related subjects.
  • Manage Pharmacovigilance, product complaints, non-compliant products and processes in collaboration with Global RA, Global QA, and commercial teams.
  • Manage people, budget and resources of Regulatory Affairs.
  • Support Regional QA to ensure that company and distributor warehouses meet global standard.
  • Focus on new product registration and paper work.

Experience | Skill Requirements

  • Bachelor's degree in Pharmacy
  • Must be familiar with Regulatory environment, and have an understanding of labeling regulations and controls.
  • 5-10 years' experience in regulatory affairs and product registration management,
  • Must be able to interact with internal Client teams and manufacturing site personnel in a professional manner.
  • QA knowledge & experience as an asset.
  • Solid work experience with Multi-National Companies in Pharmaceutical experience.

Please note that we can only accept applications from candidates with current working permission in Thailand, and that due to the expected high application rate, only those who are shortlisted will be contacted.

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