le="text-align: center;">MPharm Job Opportunity at Accenture – LifeScience Regulatory Services Associate, Apply Now!
Looking to begin or elevate your career in regulatory affairs within the life sciences sector? Accenture is hiring a LifeScience Regulatory Services Associate in Bengaluru! Ideal for freshers and professionals with up to 3 years of experience, this full-time role offers a chance to work with a global leader in digital transformation. If you hold a Master’s degree in Pharmacy (M.Pharm) and are passionate about regulatory strategy, submission preparation, and compliance with ICH and global health authority regulations, this opportunity is made for you. Apply now and join Accenture’s mission of delivering human ingenuity and tech-powered innovation in healthcare.
- Job Position: LifeScience Regulatory Services Associate
- Location: Bengaluru
- Experience: 0–3 years
- Qualification: Master of Pharmacy (M.Pharm)
- Job ID: AIOC-S01579887
- Shift: May require rotational shifts
About the Company:
Accenture is a global professional services powerhouse specializing in digital, cloud, security, strategy, consulting, technology, and operations. With over 775,000 employees serving clients in 120+ countries, Accenture is at the forefront of innovation, helping businesses transform and thrive in a dynamic digital world. Known for its inclusive culture, forward-thinking vision, and commitment to continuous learning, Accenture is consistently ranked among the World’s Best Workplaces™.
MPharm Job Opportunity at Accenture – Description:
As a LifeScience Regulatory Services Associate, you’ll be part of Accenture’s Life Sciences R&D vertical. You will work with top biopharma clients, supporting their regulatory submission lifecycle management (LCM), authoring, compliance checks, and document control in alignment with ICH guidelines and other global health authority standards. You’ll use Veeva Vault and other regulatory tools to streamline operations, enhance submission quality, and ensure legal and scientific requirements are met.
Key Responsibilities:
- Perform regulatory affairs lifecycle management (LCM) using tools like Veeva Vault
- Transform and review source documents for regulatory submissions
- Conduct quality control (QC) checks for all submission components
- Support regulatory submission strategy, authoring of CMC documents, and HA packages
- Provide guidance on scientific and legal regulatory requirements
- Ensure product compliance with current regulatory frameworks
- Participate in data collation, evaluation, and document preparation
- Collaborate with internal teams and supervisors to meet submission deadlines
- Handle tasks independently with structured instruction for new assignments
MPharm Job Opportunity at Accenture – Requirements:
- Education: Master’s in Pharmacy (M.Pharm)
- Experience: 0 to 3 years in regulatory affairs, preferably in the life sciences or pharma sector
- Familiarity with ICH guidelines, Veeva Vault, and global health authority submission processes
- Strong analytical, problem-solving, and documentation skills
- Detail-oriented with the ability to follow standard procedures
- Effective communication skills and ability to work in a team environment
- Willingness to work in rotational shifts if required
Desired Skills:
- Life Sciences Regulatory Services
- Regulatory Compliance & Documentation
- Veeva Vault or similar platforms
- Life Sciences Automation Enablement
- Data Quality Checks
- Analytical & Problem-Solving
- Results Orientation
- Attention to Detail
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