Azelis has announced new Regulatory Affairs and Regulatory Information Management job openings in Mumbai for professionals interested in product regulatory data, Safety Data Sheet (SDS) authoring, product information management, compliance documentation and regulatory operations.
The latest Azelis Mumbai hiring 2026 includes three positions: Senior Associate โ Regulatory Information Management, Process Lead โ Regulatory Information Management, and Senior Associate โ SDS Authoring.
These opportunities are particularly relevant for candidates with backgrounds in Pharmacy, Chemistry, Chemical Sciences, Life Sciences, Regulatory Affairs, Product Stewardship, SDS Authoring, RIM, PIM or related disciplines, depending on the position and the employer’s screening criteria.
Candidates should note that the supplied Azelis job descriptions focus heavily on responsibilities and competencies and do not explicitly state degree requirements or years of experience. Therefore, the qualifications below are presented as likely/relevant backgrounds rather than confirmed mandatory eligibility.
1. Senior Associate โ Regulatory Information Management
Requisition ID: R7929
Location: Mumbai, India
The Senior Associate โ Regulatory Information Management role focuses on maintaining accurate and compliant product information within Product Information Management (PIM) systems. The professional will support new product creation, product enrichment, regulatory documentation, data integrity and quality-control activities.
Key Responsibilities
- Execute new product creation and product updates/enrichment in PIM.
- Ensure product records are complete, accurate and processed according to established workflows.
- Verify appropriate linkage of product records with regulatory and technical documents.
- Incorporate approved regulatory, trade-control and documentation changes into product records.
- Maintain regulatory and technical documentation such as specifications, compliance statements, certificates, declarations and technical data sheets.
- Identify missing, inconsistent, outdated or incomplete regulatory documentation.
- Conduct self-checks, peer checks and defined quality-review activities.
- Support resolution of non-conformities and documentation gaps.
- Maintain audit-ready documentation, version control and traceability.
- Respond to RIM-related stakeholder queries.
- Maintain trackers and operational records for service governance.
- Identify recurring issues and support continuous process improvement.
Relevant Qualifications
Candidates with the following educational backgrounds may be relevant:
- B.Pharm / M.Pharm
- B.Sc / M.Sc Chemistry
- B.Sc / M.Sc Life Sciences
- Pharmaceutical Sciences
- Chemical Sciences
- Regulatory Affairs or related scientific disciplines
Important: Azelis has not explicitly specified the mandatory degree in the supplied job description.
Key Skills
- Regulatory Information Management (RIM)
- Product Information Management (PIM)
- Regulatory documentation
- Product data management
- Data integrity and traceability
- Version control
- Quality checks
- Compliance documentation
- Audit readiness
- Stakeholder coordination
2. Process Lead โ Regulatory Information Management
Requisition ID: R7927
Location: Mumbai, India
The Process Lead โ Regulatory Information Management position has broader operational ownership. The successful candidate will coordinate daily RIM execution, manage workload distribution, monitor backlogs and quality metrics, and support implementation of regulatory changes across product-information workflows.
Key Responsibilities
- Lead daily Regulatory Information Management execution for the assigned region.
- Coordinate new product creation and product enrichment activities in PIM.
- Assign work and balance operational workloads.
- Manage product setup, document updates, quality checks and stakeholder queries.
- Ensure compliance with work instructions, checklists and approval workflows.
- Maintain data integrity and audit readiness across product records.
- Ensure current regulatory and technical documentation is connected with relevant product records.
- Drive peer reviews, sampling checks and validation controls.
- Support implementation of regulatory requirements including GHS, CLP and transport regulations.
- Coordinate with PSRA Specialists on regulatory and compliance checks.
- Manage request intake, prioritization and backlog control.
- Monitor ageing requests and escalate operational risks.
- Track throughput, SLA/TAT, backlog and quality trends.
- Support integration and regulatory projects.
- Drive improvements in cycle time, standardization, rework reduction and data quality.
Relevant Qualifications
Potentially relevant educational backgrounds include:
- B.Pharm / M.Pharm
- B.Sc / M.Sc Chemistry
- Pharmaceutical Sciences
- Chemical Sciences
- Life Sciences
- Regulatory Affairs
- Related scientific or technical disciplines
Because this is a Process Lead position involving work allocation, regulatory implementation and operational performance management, candidates with prior RIM, regulatory operations, product stewardship, chemical regulatory or PIM experience are likely to be more competitive.
Key Skills
- Regulatory Information Management
- PIM systems
- Regulatory operations
- GHS
- CLP
- Transport regulations
- Product stewardship
- Data quality management
- SLA/TAT management
- Backlog management
- Team/workload coordination
- Regulatory change management
- Continuous improvement
- Stakeholder management
3. Senior Associate โ SDS Authoring
Requisition ID: R7928
Location: Mumbai, India
The Senior Associate โ SDS Authoring role is focused on Safety Data Sheet preparation, hazard communication and chemical regulatory compliance.
Candidates with experience or knowledge of SDS authoring, GHS, CLP, chemical classification, labelling and transport classification are particularly relevant to this opportunity.
Key Responsibilities
- Author and update compliant Safety Data Sheets for assigned products and regions.
- Apply appropriate classification, labelling and SDS content requirements.
- Use approved regulatory data sources, templates and authoring-system logic.
- Conduct technical checks of SDS classification and content.
- Verify SDS section completeness and regulatory phrasing.
- Apply GHS, CLP and transport classification requirements.
- Support regional hazard communication requirements across EMEA, APAC and AMER.
- Implement updated regulatory rules, classifications, phrases and templates.
- Coordinate complex regulatory questions with Process Leads and Specialists.
- Maintain SDS records with appropriate version control and traceability.
- Identify missing, outdated or inconsistent technical information.
- Conduct self-checks and peer quality reviews.
- Support corrective and preventive actions related to quality findings.
- Identify recurring SDS errors and recommend process improvements.
- Respond to SDS-related stakeholder queries.
- Maintain operational trackers and governance records.
Relevant Qualifications
This position may particularly suit candidates from:
- B.Pharm / M.Pharm
- B.Sc / M.Sc Chemistry
- B.Sc / M.Sc Chemical Sciences
- Pharmaceutical Sciences
- Industrial Chemistry
- Toxicology
- Environmental Science
- Regulatory Affairs
- Other relevant scientific disciplines
The official description provided does not specify an exact mandatory degree, so candidates should verify eligibility on the Azelis application page.
Key Skills
- Safety Data Sheet (SDS) Authoring
- GHS
- CLP Regulation
- Hazard communication
- Chemical classification and labelling
- Transport classification
- Chemical regulatory compliance
- Product stewardship
- Regulatory documentation
- SDS quality review
- Data integrity
- Version control
- Regulatory change implementation
Which Candidates Should Consider These Azelis Jobs?
These Azelis regulatory jobs in Mumbai may be relevant for professionals working in or seeking career growth across:
Regulatory Information Management | Regulatory Operations | Product Stewardship | Chemical Regulatory Affairs | SDS Authoring | Hazard Communication | PIM | Product Data Management | Regulatory Documentation
Candidates should choose the position according to their existing expertise. The RIM Senior Associate role emphasizes product and regulatory data execution, while the Process Lead position adds operational ownership and performance management. The SDS Authoring role is substantially more specialized toward chemical hazard communication and classification.
Experience Required
The supplied job descriptions do not specify an exact number of years of experience.
However, the titles Senior Associate and particularly Process Lead indicate that these are unlikely to be pure fresher positions. Relevant professional experience in RIM, PIM, SDS authoring, regulatory operations, product stewardship, chemical compliance or related functions is likely to strengthen an application.
Candidates should avoid representing an inferred experience range as an official Azelis requirement.
Why Consider Azelis Regulatory Careers?
These positions provide exposure to regulatory information and product compliance activities spanning EMEA, APAC and AMER. Depending on the role, professionals may gain experience with RIM/PIM workflows, regulatory documentation, SDS authoring, GHS/CLP requirements, data-quality controls and international stakeholder management.
The roles may be particularly useful for professionals building careers in global regulatory operations, product stewardship, chemical regulatory compliance and regulatory information management.
How to Apply
Candidates should review the official job description carefully before submitting their application.
Senior Associate โ Regulatory Information Management (R7929):
Apply
Process Lead โ Regulatory Information Management (R7927):
Apply
Senior Associate โ SDS Authoring (R7928):
Apply