Genpact is inviting applications for the position of Associate – Regulatory Affairs Operations at its Gurugram location. This opportunity is suitable for candidates looking to build a career in Regulatory Affairs, Drug Regulatory Affairs, regulatory compliance, and pharmaceutical regulatory operations.
Candidates with a Bachelor’s in Pharmacy (B.Pharm), Health Administration, Healthcare, Master’s in Public Health, or Master’s in Regulatory Affairs are eligible as specified in the job description. The vacancy indicates 0–2 years of experience, making it particularly relevant for early-career professionals seeking Regulatory Affairs jobs in the pharmaceutical and healthcare sector.
Job Overview
Company: Genpact
Position: Associate – Regulatory Affairs Operations
Location: Gurugram, Haryana
Experience: 0–2 Years
Employment Type: Full-Time, Permanent
Openings: 4
Functional Area: Regulatory Affairs / Regulatory Operations / Compliance
Salary: Not disclosed by the employer
Key Responsibilities
As an Associate in Regulatory Affairs Operations at Genpact, selected candidates may be responsible for:
- Conducting regulatory compliance audits and reviews.
- Developing and implementing compliance policies and procedures.
- Monitoring changes in applicable regulations and updating internal policies accordingly.
- Collaborating with internal stakeholders to ensure regulatory and compliance requirements are met.
- Providing compliance-related training to employees.
- Investigating and resolving regulatory compliance issues.
- Preparing compliance reports and recommendations for management.
- Supporting regulatory documentation and operational compliance activities.
Qualifications
According to the job description, candidates with the following educational backgrounds can apply:
- Bachelor’s in Pharmacy (B.Pharm)
- Bachelor’s in Health Administration
- Bachelor’s in Healthcare
- Master’s in Public Health (MPH)
- Master’s in Regulatory Affairs
The listing also mentions B.Sc Chemistry and B.Pharm in Pharmaceutical Analysis and Quality Assurance under its education section.
Candidates should carefully verify their specific qualification against the employer’s application page before applying.
Preferred Regulatory Affairs Skills
Knowledge or experience in the following areas may strengthen a candidate’s profile:
Regulatory Affairs | Drug Regulatory Affairs | Regulatory Submissions | CTD | eCTD | ICH Guidelines | XEVMPD | IDMP | Regulatory Reports | Document Review | DocuBridge | Liquent | Pharmaceutical Regulations
Understanding regulatory documentation, compliance procedures and pharmaceutical regulatory submissions can be particularly valuable for this role.
Why Consider This Genpact Regulatory Affairs Job?
This position provides an opportunity to work in Regulatory Affairs Operations while developing experience in regulatory compliance, audits, documentation, policies and stakeholder coordination.
Genpact highlights opportunities for continuous learning, mentorship, digital innovation and exposure to global enterprise operations. For B.Pharm and other eligible healthcare graduates interested in regulatory careers, this role can provide relevant industry exposure.
Who Should Apply?
This opportunity may be particularly relevant for:
- B.Pharm graduates interested in Regulatory Affairs
- Regulatory Affairs professionals with up to 2 years of experience
- Public Health and Healthcare graduates
- Candidates interested in pharmaceutical regulatory operations
- Candidates familiar with CTD/eCTD and regulatory submissions
- Early-career professionals seeking Regulatory Affairs jobs in Gurugram
How to Apply
