Back to list

Vacancy description

Associate Consultant-SDS Author/ Regulatory Documentation Specialist (10-15 Years) in Bangalore, भारत

  • Full-timeStandard weekly hours

$14.68 USD

Bangalore, भारत

Associate Consultant-SDS Author/ Regulatory Documentation Specialist (10-15 Years)

Position Description
Company Profile:
Founded in 1976, CGI is among the largest independent IT and business consulting services firms in the world. With 94,000 consultants and professionals across the globe, CGI delivers an end-to-end portfolio of capabilities, from strategic IT and business consulting to systems integration, managed IT and business process services and intellectual property solutions. CGI works with clients through a local relationship model complemented by a global delivery network that helps clients digitally transform their organizations and accelerate results. CGI Fiscal 2024 reported revenue is CA$14.68 billion and CGI shares are listed on the TSX (GIB.A) and the NYSE (GIB). Learn more at cgi.com.

Position: Associate Consultant-SDS Author/ Regulatory Documentation Specialist
Experience: 10-15 years
Category: Software Development/ Engineering
Shift Timing: 1:00 PM-10:00 PM
Location: Bangalore/Hyderabad/Chennai Pune/Mumbai
Position ID: J0926-0495
Employment Type: Full Time

Education Qualification: Bachelor’s or master’s in chemistry, Toxicology, Environmental Science, or a related field.

We are seeking a highly detail-oriented SDS Author with expertise in global chemical regulatory standards. You will be responsible for authoring, reviewing, and maintaining Safety Data Sheets (SDS), labels, and related hazard communication documents using various authoring platforms.

Your future duties and responsibilities
• Work with US client on a daily basis to create and update SDSs, labels, and hazard communication documents using SDS authoring platforms such as ProSteward360, SAP EHS, and Sphera.
• Ensure compliance with GHS, REACH, CLP, OSHA HCS, WHMIS, and other global chemical regulations.
• Interpret chemical and toxicological data to ensure accurate classifications and hazard statements.
• Collaborate with regulatory, toxicology, and product teams for data validation and approval.
• Maintain version control and support multi-language document generation and localization.
• Monitor regulatory changes and update documentation accordingly.
• Deliver timely SDS updates and improve safety outcomes.
• Perform peer quality reviews to report errors and improve overall performance.
• Ability to train other SDS Authors on platform and business processes.

Required qualifications to be successful in this role
Must to have skills-

7+ years of experience in SDS authoring or chemical regulatory compliance.
• Knowledge of global SDS formats and regional classification systems.
• Experience with PS360 or similar SDS authoring platforms (The WERCS, Intelligent Authoring, MSDGen, SAP EHS)
• Familiarity with chemical databases (e.g., IUCLID, ChemIDplus).
• Ability to work US based hours (8am -5pm EST)
• Communicate directly with the customer on a daily basis on specific authoring tasks

• Certified SDS Author (AIHA, SDSRP, or equivalent)
• Dangerous good transport certification (DG)
• Exposure to SAP EHS, REACH registration systems, or Poison Centre Notification tools.
• Using task management software (JIRA, etc.) to track and prioritize tasks to timely complete

Good to have Skills-

• Experience with Sphera - SAP EHS solutions is a strong advantage.
• Experience in the Oil & Gas industry would be an added advantage.

Together, as owners, let’s turn meaningful insights into action.

Life at CGI is rooted in ownership, teamwork, respect and belonging. Here, you’ll reach your full potential because…

You are invited to be an owner from day 1 as we work together to bring our Dream to life. That’s why we call ourselves CGI Partners rather than employees. We benefit from our collective success and actively shape our company’s strategy and direction.

Your work creates value. You’ll develop innovative solutions and build relationships with teammates and clients while accessing global capabilities to scale your ideas, embrace new opportunities, and benefit from expansive industry and technology expertise.

You’ll shape your career by joining a company built to grow and last. You’ll be supported by leaders who care about your health and well-being and provide you with opportunities to deepen your skills and broaden your horizons.

That same commitment to fairness extends to how we use technology. To support our recruitment team, AI tools may be used to help assess applications though they never replace human judgement. All hiring decisions remain entirely in the hands of our recruitment professionals.

Come join our team—one of the largest IT and business consulting services firms in the world.

Similar vacancies

More like this role

  • Full-time
  • Contract
Position Title: Specialist - Project Documentation Role Overview We are looking for Project Documentation Specialist to join our global Customer Documentation team in India. The role is responsible for the correct archiving, compilation, follow-up, and delivery of customer documentation during live projects, ensuring full ...

Chennai, भारत

  • Contract
... covers end-to-end business needs. You’ll make a difference by: - The Document Administrator will support end-to-end delivery coordination of MSDAC products and associated site requirements. The role involves managing documentation, vendor coordination, inspection support, dispatch planning, and ensuring material availability ...

Bombay, भारत

  • Contract
... Timely, effective and transparent communication with global stakeholders for all requests Technical expertise - - High standard of technical understanding of regulatory requirements for raw materials within all categories of use (Cosmetics, OTC, Drugs, Food/Nutritional’s etc.) - Knowledge of toxicology & safety assessment ...

Bangalore, भारत

  • Full-time
  • Contract
  • Medicine
  • Auditing
... knowledge on local and imported Pharmaceutical and Biological products to facilitate dossier development and registration. - Developing good rapport with Regulatory authorities and ensuring proper co-ordination to obtain licenses. - Keeping the team motivated irrespective of Regulatory hurdles faced during the Registration ...

Pune, भारत

  • Contract
... supervise regulatory affairs team; establish processes and provide guidance - Coordinate with quality, marketing, and international departments on compliance and documentation Requirements - BVSc & AH or related science degree; PGDMM preferred - 15 years experience in ethical veterinary pharmaceutical market - Technical knowledge ...

Pune, भारत

  • Remote
  • Full-time
... competence pertaining to regulatory knowledge like pharamcopoeial requirements (USP EP JP ChP) regulatory guidelines issued by EU USA China Canada ICH & other health authorities Keep abreast with the new updates from Health Authorities like FDA warning letters authorization of innovative products etc. Provide regulatory support ...

Satara, भारत

  • Full-time
... Qualifications Good Communication Skills Educational background: Masters in food science, food technology, nutritional science or similar Industry experience: 3-5+ years in conducting food regulatory compliance checks globally Nice to have: Experience using TraceOne and IOFI database Mindset: Customer-focus; accurate working ...

Pune, भारत

Thermo Fisher Scientific

Regulatory Affairs Specialist

  • Contract
Regulatory Affairs Specialist at Thermo Fisher Scientific supporting preparation of regulatory documentation and submissions under EUCTR guidance. The role involves coordinating client deliverables, managing project communications, and ensuring compliance with regulatory standards and internal procedures. Responsibilities ...

Bangalore, भारत

Thomson Reuters

Content Author

  • Hybrid
  • On-site
  • Full-time
Content Author Job Description The Content Author is an entry point into the content team's career path, combining hands-on content authorship with full ownership of the content production process. This role analyzes source material from multiple resources and writes, edits, and updates clear, accurate, customer-facing ...

Hyderabad, भारत

  • Contract
  • Consulting
... processes across Product Data Management , including product classification, substance management, and compliance checks - Manage and troubleshoot Safety Data Sheet (SDS) Authoring processes, including SDS generation, versioning, and distribution workflows - Administer Hazard Label Management & Distribution , ensuring label content ...

भारत

  • Full-time
  • Contract
Regulatory and Quality Specialist Location: Gurgaon, IN Contract Type: Regular Full-Time Area: Quality Req Id: 545050 Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has ...

Bombay, भारत