Regulatory & Trade Compliance (Contract)

Merck Kgaa

Indonesia

On-site

IDR 167,400,000 - 279,000,000

Part time

7 days ago
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Job summary

Merck Kgaa is seeking a contract Regulatory & Trade Compliance specialist in Indonesia to support regulatory requirements for pharmaceutical raw materials and R&D chemicals, including import and distribution documentation.

The role involves maintaining regulatory databases, monitoring changes, coordinating with the EXIM team, and using SAP and Microsoft 365 tools to digitalize processes and build dashboards.

Qualifications

  • Bachelor’s degree in Life Science or related field.
  • 2+ years in Regulatory Affairs, Trade Compliance, Import Compliance, or Life Science/Pharma.
  • Experience with importation of pharmaceutical raw materials or lab chemicals is advantageous.
  • Strong understanding of import and trade regulations for pharma materials.
  • Familiarity with SDS/MSDS, CoA, and Technical Data Sheets.
  • Proficiency in Microsoft 365 (Excel, PowerPoint, Word, Teams, SharePoint).
  • Knowledge of Power BI, Power Automate, Microsoft Copilot, and AI tools to boost productivity.
  • Strong attention to detail, communication, and cross-functional collaboration.

Responsibilities

  • Support regulatory requirements evaluation for pharma raw materials and R&D chemicals.
  • Review regulatory docs for importation and distribution of products.
  • Maintain regulatory databases and licensing documentation.
  • Monitor regulatory changes issued by authorities.
  • Prepare regulatory documents and correspondence with authorities and stakeholders.
  • Support import licensing and trade compliance processes.
  • Review import requirements, HS Codes, and product regulatory status.
  • Coordinate with EXIM to ensure compliant import processes.
  • Utilize SAP for regulatory and trade processes.
  • Identify opportunities to digitalize Regulatory & Trade Compliance processes.
  • Develop and maintain dashboards, databases, and repositories using Microsoft 365.

Skills

Regulatory knowledge
Documentation & compliance
MS 365 proficiency
Power BI / Power Automate
Cross-functional collaboration

Education

Bachelor’s degree in Chemistry/ Chemical Engineering / Biology / Biotechnology or related Life Science

Tools

SAP
Power BI
Power Automate
Microsoft Copilot

Job description

Regulatory & Trade Compliance (Contract)

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginablewith us.

About The Role

A. Regulatory Affairs

  • Support the evaluation and fulfillment of regulatory requirements for pharmaceutical raw materials and R&D chemicals.
  • Review regulatory documentation required for the importation and distribution of products.
  • Maintain accurate and up-to-date regulatory databases and licensing documentation.
  • Monitor regulatory changes and updates issued by relevant government authorities.
  • Prepare regulatory documents, letters, and correspondence with regulatory authorities and relevant stakeholders.
  • Support import licensing and trade compliance processes.
  • Review import requirements, HS Codes, and product regulatory status.
  • Coordinate with the EXIM team to ensure smooth and compliant import processes.
  • Utilize and navigate SAP for relevant regulatory and trade compliance processes.
  • Identify opportunities to digitalize and streamline Regulatory & Trade Compliance processes.
  • Develop and maintain dashboards, databases, and document repositories using Microsoft 365.

Who you are

  • Bachelor’s degree (S1) in Chemistry, Chemical Engineering, Biology, Biotechnology, or other related Life Science disciplines.
  • Minimum 2 years of experience in Regulatory Affairs, Trade Compliance, Import Compliance, or the Life Science/Pharmaceutical industry.
  • Experience handling the importation of pharmaceutical raw materials or laboratory chemicals is a strong advantage.
  • Good understanding of import and trade regulations related to pharmaceutical raw materials and chemicals.
  • Familiarity with technical documentation such as SDS/MSDS, CoA, and Technical Data Sheets.
  • Proficient in Microsoft 365 applications, including Excel, PowerPoint, Word, Teams, and SharePoint.
  • Understanding of Power BI, Power Automate, Microsoft Copilot, and AI tools to improve workplace productivity.
  • Strong attention to detail, good communication skills, and ability to work effectively with cross-functional teams.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

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