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Regulatory Affairs Specialist, Human Pharma

The Position

 

Regulatory Affairs Specialist, Human Pharma

 

  • To achieve timely & successful product registrations in accordance with corporate & local strategies.
  • To collect any information on new Regulations and Guidelines, and to share it in local RA team.
  • To ensure compliance with Company regulatory policies, regulations & procedures.

 

Duties & Responsibilities

1. Regulatory Planning and Submission

  • Manage all the regulatory tasks & projects, including attaining, maintaining product licenses and operation licenses for assigned portfolio on behalf of Boehringer Ingelheim as required by local regulations.
  • Compile registration applications for assigned portfolio and ensure timely approval.
  • Monitor progress of submissions & coordinate timely responses to all questions from the health authorities.
  • Be Compliant with Corporate policies, regulations & procedures, in particular implementation of current Company Core Data Sheet (CCDS), Change Review Committee (CRC) and local change control procedures

2. Regulatory Intelligence and Interaction

  • Responsible to collect new or updated local regulations via various potential sources and keep the local RA team and ROPU informed
  • Communicate with Regulatory Authorities and local industry groups on regulatory issues

3. Cross-functional collaboration and support

  • Provide regulatory consultation & collaborate with  local business stakeholders
  • Provide feedback to the implementation of global initiatives when required

4. Quality and Compliance

  • Timely submission of CCDS, CRC, Renewals, PSUR and other local variations in compliance with internal KPIs
  • Ensures that regulatory database is up to date to  reflect the current registration status or regulatory requirements
  • Support local inspection readiness
  • Archiving of local regulatory submission documents

 

Requirements

Minimum Education / Degree Requirements: Bachelor’s degree in Pharmacy preferred

Skills required:

  • Good knowledge of National Drug Regulations and Procedures
  • Good communication skills for internal & external interactions
  • Proactive and assertive attitude
  • English proficiency
  • Good computer literacy skills, comfortable working with databases

Experience: Minimum 3 years of experience working in the pharmaceutical, medical device or healthcare industry with strong performance record in the previous position.

 

READY TO CONTACT US?

Please contact our Recruiting Team: Ms. Phuong Vo: phuong.vo@boehringer-ingelheim.com

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