CGI Hiring Regulatory Analyst Professionals

CGI Hiring Regulatory Analyst Professionals | Pharma & Regulatory Affairs Jobs

Looking for Regulatory Affairs jobs in Bangalore, Hyderabad, or Chennai? CGI is currently hiring experienced Pharma and Regulatory Affairs professionals for the role of Junior Regulatory Analyst. This opportunity is ideal for candidates with experience in regulatory publishing, eCTD submissions, RIM systems, quality checks, and pharma compliance operations. Professionals with expertise in pharmaceutical regulatory affairs, drug submission management, data migration, and compliance documentation can explore this full-time opportunity with one of the world’s leading IT and business consulting firms.

The demand for Regulatory Affairs specialists, pharmacovigilance experts, and life sciences compliance professionals continues to rise across India’s healthcare and pharmaceutical sectors. CGI’s latest hiring drive offers candidates exposure to global regulatory environments, digital transformation projects, regulatory software tools, and end-to-end pharmaceutical submission processes.

Company Overview

entity[“company”,”CGI”,”Global IT and business consulting company”] is one of the world’s largest independent IT and business consulting services organizations. Founded in 1976, the company has built a strong reputation across healthcare technology, life sciences consulting, digital transformation, cloud solutions, and enterprise business services.

With more than 94,000 professionals worldwide, CGI supports organizations through strategic consulting, systems integration, regulatory technology services, managed IT operations, and business process solutions. The company reported fiscal revenue of CA$14.68 billion in 2024 and operates through a global delivery network supporting industries including pharmaceuticals, healthcare, biotechnology, banking, insurance, and manufacturing.

CGI is widely recognized for its employee-first culture, ownership-driven work environment, and long-term career development opportunities. The organization provides employees with access to advanced technologies, regulatory compliance projects, and global healthcare consulting assignments.

Professionals joining CGI’s regulatory affairs division can gain exposure to pharmaceutical compliance systems, eCTD lifecycle management, regulatory information management platforms, and digital publishing tools used by global healthcare companies.

Job Role & Responsibilities

CGI is hiring candidates for the position of Junior Regulatory Analyst under the Business Analysis and Regulatory Affairs domain. This role focuses on supporting regulatory operations, publishing activities, submission management, RIM-related functions, compliance processes, and cross-functional coordination between technical and business teams.

Candidates selected for this Regulatory Affairs job will work on pharmaceutical submission workflows, quality control activities, regulatory documentation, labeling support, and data migration operations.

Key Responsibilities

• Support requirement gathering activities alongside business analysts and technical stakeholders
• Assist in preparing mapping documents for regulatory data migration and cleansing activities
• Coordinate with technical teams during implementation and validation support processes
• Support regulatory publishing activities including eCTD, NeeS, and paper format submissions
• Assist in CMC authoring, compliance documentation, regulatory labeling, and quality control activities
• Perform quality checks and help resolve publishing or submission-related issues
• Support Regulatory Information Management (RIM) system activities and migration tasks
• Ensure timely submission delivery according to regulatory compliance standards
• Maintain proper regulatory documentation and workflow tracking
• Collaborate with global regulatory teams for submission management activities

Required Technical Skills

Candidates applying for this pharmaceutical regulatory affairs role should possess practical knowledge of:

• Regulatory Affairs processes
• eCTD publishing
• NeeS submission formats
• Paper-based regulatory submissions
• Regulatory compliance workflows
• Regulatory labeling systems
• Quality control documentation
• Data migration concepts
• Pharmaceutical submission management
• Healthcare compliance standards
• Regulatory software tools

Preferred Tools Exposure

CGI prefers candidates with hands-on experience or exposure to the following regulatory platforms and software tools:

• SmartDesk
• ISI Toolbox
• ACUTA RIM
• Veeva Vault
• Lorenz
• Insight Suite

Candidates with knowledge of global regulatory standards, RIM systems, pharmacovigilance compliance, and international healthcare submission requirements will have an added advantage.

Eligibility / Qualifications

Candidates interested in this Regulatory Analyst vacancy should meet the following educational and experience requirements.

Educational Qualification

Applicants must possess a Bachelor’s degree in Pharmacy or a related life sciences discipline with relevant industry experience.

Eligible educational backgrounds include:

B.Pharm, M.Pharm, Pharm.D, MSc, M.Sc Life Sciences, Biotechnology, Biochemistry, Microbiology, Clinical Research, Pharmaceutical Sciences, Healthcare Management, Regulatory Affairs, Life Science graduates, or related healthcare and pharmaceutical disciplines.

Experience Required

• Minimum Experience: 3 Years
• Maximum Experience: 5 Years
• Industry Preference: Pharma, Clinical Research, Regulatory Affairs, Healthcare IT, Life Sciences Consulting

Essential Skills

• Strong analytical thinking abilities
• Good communication and documentation skills
• Experience in regulatory publishing and submissions
• Understanding of pharma compliance standards
• Knowledge of quality control workflows
• Familiarity with healthcare data migration concepts
• Exposure to global regulatory environments

Candidates with prior experience in pharmaceutical compliance jobs, healthcare consulting, regulatory operations, submission publishing, and life sciences technology projects are encouraged to apply.

Location & Salary

Job Location

Bangalore / Hyderabad / Chennai

Salary

Salary package for this Regulatory Affairs role will be competitive and based on candidate experience, technical expertise, pharmaceutical regulatory knowledge, and interview performance.

Application Process

Candidates interested in this Pharma Regulatory Affairs opportunity can apply online through the official CGI careers portal.

Apply Here: Careers Application Link https://cgi.njoyn.com/corp/xweb/xweb.asp?CLID=21001&page=jobdetails&JobID=J0526-0898&lang=1

Frequently Asked Questions (FAQs)

1. What is the job role offered by CGI?

CGI is hiring candidates for the position of Junior Regulatory Analyst under the Regulatory Affairs and Business Analysis domain.

2. What qualifications are required for this CGI Regulatory Affairs job?

Candidates with B.Pharm, M.Pharm, Pharm.D, MSc, Biotechnology, Clinical Research, Biochemistry, Microbiology, and related life sciences qualifications are eligible.

3. How much experience is required for this role?

Applicants should have 3 to 5 years of relevant experience in Regulatory Affairs, eCTD publishing, compliance operations, or regulatory submissions.

4. Which locations are available for this job?

The job locations include Bangalore, Hyderabad, and Chennai.

5. What regulatory tools are preferred for this position?

Candidates with experience in Veeva Vault, Lorenz, SmartDesk, ISI Toolbox, ACUTA RIM, and Insight Suite will have an advantage.

6. Is this a full-time job opportunity?

Yes, CGI is offering this position as a full-time employment opportunity.

Summary Table

Category	Details
Company	CGI
Department Vacancies	Junior Regulatory Analyst, Regulatory Affairs, Business Analysis
Qualification	B.Pharm, M.Pharm, Pharm.D, MSc, Biotechnology, Biochemistry, Clinical Research, Microbiology, Life Sciences
Experience	3–5 Years
Location	Bangalore / Hyderabad / Chennai

Tagged as: Pharma Jobs in Bangalore, Pharma Jobs in Hyderabad