Sourabh Vishwakarma

Operations Associate

Mumbai, Maharashtra, India8 mos experience

Key Highlights

M.Sc. Organic Chemistry graduate with high CGPA.
Hands-on experience with HPLC at FDA.
Strong background in Quality Assurance and Regulatory Affairs.

Stackforce AI infers this person is a Quality Assurance and Regulatory Affairs specialist in the pharmaceutical industry.

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Skills

Core Skills

Quality AssuranceRegulatory ComplianceRegulatory AffairsQuality Control

Other Skills

Data OperationsBilling ProcessCollaborationData IntegrityAnalytical SkillsRegulatory KnowledgePharmaceutical StandardsGood Manufacturing Practices (GMP)Drug DevelopmentCompliance DocumentationPharmaceutical AnalysisResearch & Development (R&D)Polymer EngineeringPolymer ChemistryFormulation

About

I am an M.Sc. Organic Chemistry graduate (CGPA: 8.83) with hands-on experience in analytical testing during a two-month internship at the Food & Drugs Administration (FDA) and quality documentation support work at the Bureau of Indian Standards (BIS). I possess strong skills in laboratory practices, regulatory documentation, GDP, and compliance support, and I seek opportunities in Quality Assurance, Regulatory Affairs, or Export Documentation within the pharmaceutical or chemical industry.

Experience

Bureau of indian standards

Quality assurance and data operations

Jan 2025 – Sep 2025 · 8 mos · Powai · On-site

As a Data Operations & Billing Specialist at the Bureau of Indian Standards (BIS), I handle the reconciliation of laboratory bills, ensuring accuracy and compliance. I manage the complete billing process, from invoicing to record maintenance, and oversee data operations, ensuring the accurate input and processing of critical data. I also collaborate with teams to maintain smooth operations and data integrity, while proactively addressing discrepancies and generating reports to support decision-making and process improvements.

Regulatory ComplianceQuality AssuranceData OperationsBilling ProcessCollaborationData Integrity

Fda : food & drug administration

Intern Research analyst

Apr 2023 – Jun 2023 · 2 mos · Bandra, Maharashtra, India · On-site

As an intern at the FDA Bandra , I had the opportunity to work on various projects related to the standards and research of pharmaceutical products such as tablets, syrups, and capsules. This experience allowed me to gain valuable insights into the regulatory and quality control aspects of the pharmaceutical industry.

Analytical SkillsRegulatory KnowledgePharmaceutical StandardsQuality ControlRegulatory Affairs