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Senior Analyst - Product Stewardship/Regulatory Toxicology

Merck Kgaa
Merck KGaA
3-4 years
Not Disclosed
10 Jan. 5, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Analyst – Product Stewardship / Regulatory Toxicology

Job ID: 294385
Location: Bangalore, Karnataka, India
Employment Type: Full-time


About the Organization

We are a global science and technology-driven organization committed to improving quality of life through innovative solutions in Healthcare, Life Science, and Electronics. With a strong global footprint and diverse teams, we foster a culture of curiosity, collaboration, and excellence. Our people are united by a shared purpose: to imagine the unimaginable and deliver responsible, sustainable, and compliant solutions that benefit customers, patients, and the planet.


Role Overview

The Senior Analyst – Product Stewardship / Regulatory Toxicology will play a key role in ensuring regulatory compliance of products through accurate hazard classification, Safety Data Sheet (SDS) authoring, and effective implementation of global chemical regulations. This position requires strong regulatory knowledge, analytical capability, and collaboration with international stakeholders across regions.


Key Responsibilities

  • Interpret and apply global chemical regulations such as CLP, GHS, and related regional regulatory frameworks.

  • Create, review, and maintain compliant Safety Data Sheets (SDS) through in-depth data research and toxicological evaluation.

  • Perform accurate data entry and maintenance within SAP EHS systems in alignment with regulatory and internal standards.

  • Understand and apply CLEO content and rule sets for hazard classification and labeling decisions.

  • Manage and respond to internal and external customer inquiries, including handling regulatory change requests.

  • Support regulatory and product stewardship projects at country, regional, and global levels.

  • Identify, propose, and implement continuous process improvements to enhance efficiency and data quality.


Required Qualifications and Experience

Education

  • Master’s degree in Chemistry, Toxicology, Pharmacy, or other relevant scientific disciplines.

Experience

  • 3 to 4 years of professional experience in Regulatory Affairs, Product Stewardship, or Regulatory Toxicology.

  • Hands-on experience with Safety Data Sheet authoring and hazard classification.

  • Proven experience working with SAP EHS or similar regulatory compliance systems.


Skills and Competencies

  • Strong understanding of global chemical compliance regulations and hazard communication requirements.

  • Excellent analytical and problem-solving skills with attention to detail.

  • Strong written and verbal communication skills with a good command of English.

  • Ability to collaborate effectively with international and cross-functional teams.

  • Proactive, result-oriented, and capable of working in complex and dynamic environments.

  • High learning agility and a strong team-oriented mindset.


What We Offer

  • A diverse, inclusive, and globally connected work environment.

  • Opportunities for continuous professional development and career progression.

  • Exposure to global regulatory projects and international stakeholders.

  • A culture that values innovation, scientific rigor, and responsible product stewardship.


Apply Now

Advance your career in Regulatory Toxicology and Product Stewardship by joining a team committed to scientific excellence, regulatory compliance, and sustainable innovation.