Accenture Pharma Associate Job Openings – Apply Online
LifeScience Regulatory Svs Associate
Bengaluru
Job No.: aioc-s01552749
Job Type: Full-time
Job Description
Skill required: Regulatory Services – Life Sciences Regulatory Affairs
Designation: LifeScience Regulatory Svs Associate
Qualifications: Master of Pharmacy
Years of Experience: 1 to 3 years
About Accenture
Accenture is a global professional services company with leading capabilities in digital, cloud, and security. Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song—all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners, and communities. Visit us at www.accenture.com
What would you do?
You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise and regulatory services. Employees in this area are part of the Regulatory sub-offerings, helping the world’s leading biopharma companies bring their vision to life by enabling them to improve outcomes by converging around
the patient and connecting scientific expertise with unique insights into the patient experience.The incumbent will:
- Perform regulatory operations tasks for life cycle maintenance (documents) of submission in accordance with ICH guidelines and other Health Authorities.
- Review and transform Source Documents.
- Perform Quality Control (Document QC) checks for all submission components.
- Collect, collate, evaluate, and build dossiers.
- Ensure the organization’s products comply with current regulations.
- Examples include building regulatory submission strategy, authoring CMC documents, and preparing health authority packages.
What are we looking for?
- Experience in building Regulatory Dossiers for Life Cycle Management.
- Familiarity with Veeva Regulatory Module.
Roles and Responsibilities:
- Solve routine problems, largely through precedent and general guidelines.
- Expected interactions are within your own team and direct supervisor.
- Receive detailed to moderate levels of instruction on daily tasks and detailed instruction on new assignments.
- Decisions will impact your own work.
- Act as an individual contributor within a focused scope of work.
- Note: This role may require rotational shifts.
Qualifications: Master of Pharmacy
Link to apply: APPLY ONLINE HERE
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