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Regulatory Affairs & Compliance Analyst

0-2 years
Not Disclosed
10 Jan. 31, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

πŸ“Œ Regulatory Affairs & Compliance Analyst | Diversey
πŸ“ Location: Mumbai, India
πŸ’Ό Time Type: Full-time
πŸ—“ Posted: 2 Days Ago | Deadline: May 31, 2025 (30+ days left to apply)

🌍 About Diversey

Diversey is a global leader in providing cleaning and hygiene products, solutions, and services that support the safety and well-being of people, the environment, and communities. We focus on delivering value by ensuring compliance with global regulations and maintaining high-quality standards for our products.

πŸ“ About the Role

As a Regulatory Affairs & Compliance Analyst, you will be responsible for handling key regulatory activities, including compliance workflows, Safety Data Sheets (SDS) authoring, product registrations, renewals, and more. You will ensure the regulatory compliance of Diversey products by working on various global hazard communication regulations. You will be reporting to the Manager of Regulatory Affairs.

πŸ” Key Responsibilities

Regulatory Compliance & Safety Data Sheets

βœ” SDS Authoring: Create Safety Data Sheets for multiple global geographies as per applicable hazard communication regulations.
βœ” Hazard Classification: Derive hazard classifications for substances and mixtures using various regulations (GHS, CLP, OSHA Hazard Communication Standard).
βœ” Compliance Reviews: Perform raw material, formula, and finished product reviews as per Globally Harmonized System (GHS) for different regions.

Coordination & Prioritization

βœ” Internal/External Queries: Address high-priority queries from internal and external stakeholders, coordinating with SMEs if needed.
βœ” Time Management: Prioritize and complete requests within defined turnaround times, ensuring records are maintained per standard formats.

Cross-functional Collaboration

βœ” Cross-functional Teamwork: Work effectively with diverse teams to ensure timely regulatory submissions and compliance.
βœ” Data Integrity: Maintain the integrity of data in SDS authoring software & ERP systems to ensure up-to-date regulatory information.

πŸ“‹ Qualifications

πŸŽ“ Education: Degree in a related field (chemical, regulatory, etc.).
πŸ“Œ Experience: Proven experience in a corporate regulatory environment with a focus on product registration, regulatory compliance, or regulatory consulting.
πŸ“Œ Expertise: Knowledge of GHS, SDS authoring, and hazard communication regulations, with experience in managing chemical regulatory documentation.
πŸ“Œ Skills: Strong communication, presentation, and analytical skills.
πŸ“Œ Languages: Proficiency in English (both verbal and written).

🌟 Desired Skills

  • Regulatory Terminology: Knowledge of the regulatory landscape and terminology.
  • Cross-Functional Skills: Ability to work both independently and in teams with minimal supervision.

πŸ“© Apply Now