Accenture Hiring – LS Regulatory Services Associate | Bangalore

ByPharma Hiring Hub

Accenture is hiring for the role of Life Sciences Regulatory Services Associate at its Bangalore location. This opportunity is suitable for B.Pharm and M.Pharm graduates with 1–3 years of experience who are looking to build or advance their career in regulatory affairs and life sciences operations.

The role focuses on supporting regulatory documentation, submission activities, compliance processes, and coordination with global teams within Accenture’s Life Sciences R&D practice. Candidates will work in a structured, process‑driven environment, supporting regulatory requirements for pharmaceutical and life sciences clients.

This position offers strong exposure to global regulatory operations, standardized workflows, and long‑term career growth within Accenture’s life sciences ecosystem

Accenture hiring for Regulatory services associate

Job Overview

  • Position: Life Sciences Regulatory Services Associate
  • Department: Regulatory affairs
  • Location: Bengaluru, Kochi, Thane
  • Experience: 1 to 3 Years
  • Qualification: B.Pharm, M.pharm
  • Job Type: Full-Time
  • Last Date to apply: not provided

Key Responsibilities – Life Sciences Regulatory Services Associate at Accenture

  • Handle routine work tasks by following established precedents, SOPs, and general regulatory guidelines.
  • Primary interactions will be within the immediate team and with the direct supervisor, ensuring clear communication and guidance.
  • Receive detailed to moderate instructions for daily activities and detailed guidance for new or unfamiliar assignments.
  • Decisions made in this role will primarily impact individual work outputs, within defined processes and oversight.
  • Work as an individual contributor within a team structure, handling a predetermined and focused scope of responsibilities.
  • Be prepared to work in rotational shifts, based on project requirements and global client support needs..

Required Skills & Qualifications

  • B.Pharm or M.Pharm degree in Pharmacy or Life Sciences.
  • 1–3 years of relevant experience in Life Sciences Regulatory Services, Regulatory Affairs, or regulatory support roles.
  • Experience supporting regulatory documentation, submissions, or compliance activities is preferred.
  • Basic to intermediate understanding of regulatory processes, submission workflows, and compliance requirements within the pharmaceutical or life sciences industry.
  • Familiarity with SOP‑driven, process‑based environments.
  • Ability to work with regulatory documents, trackers, templates, and internal systems.
  • Proficiency in Microsoft Office applications (Word, Excel, PowerPoint, Outlook).
  • Good written and verbal communication skills.
  • Ability to collaborate effectively within a team‑based, supervised work environment.
  • Comfortable working as an individual contributor within a predefined scope of work.
  • Willingness to work in rotational shifts, as required by project or client needs.
  • Ability to follow instructions, timelines, and quality standards consistently.

Why Join Accenture?

  • Join Accenture, a globally trusted organization supporting leading pharmaceutical and life sciences companies through regulatory expertise, operational excellence, and innovation.
  • Build and advance your career in Life Sciences Regulatory Services, gaining exposure to regulatory documentation, compliance support, and global submission‑related activities.
  • Work in a process‑driven, SOP‑aligned environment with clear role expectations, defined workflows, and supervised guidance—ideal for steady professional development.

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Apply Here

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.

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FAQ-Life Sciences Regulatory Services Associate at accenture

1. Who can apply for the Life Sciences Regulatory Services Associate role at Accenture?

Candidates with a B.Pharm or M.Pharm degree and 1–3 years of experience in regulatory services, regulatory affairs, or life sciences operations are eligible to apply.

2. What does this role primarily involve?

The role involves supporting regulatory documentation, compliance activities, and regulatory operations for global life sciences and pharmaceutical clients within a structured environment.

3. Is this role suitable for mid‑level professionals?

Yes. This role is suitable for early to mid‑level professionals with prior exposure to regulatory or life sciences processes who want to strengthen their regulatory operations experience.

4. Will I receive training in this role?

Yes. Accenture provides structured onboarding, task‑level guidance, and role‑specific training to support learning and performance.

5. What kind of work environment can I expect?

You will work in a process‑driven, SOP‑aligned environment with defined procedures, close supervision, and strong quality standards.

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