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Anand GauravAG
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Anand Gaurav

@anandgaurav1

I develop and scale generic solid oral dosage forms for global regulated pharmaceutical markets.

India
Message

What I'm looking for

I'm looking to contribute to pharmaceutical product development and process development, technology transfer, scale-up, regulatory documentation, and commercial launches for global regulated markets.

At MSN Laboratories, I develop generic solid oral dosage forms for US, European, ROW, and WHO markets, supporting ANDA and EU dossier submissions.

I execute pre-formulation, formulation optimization, stability, scale-up, exhibit batches, and plant-scale process development using Quality by Design. I also manage change controls and prepare CMC, MFR, BOM, BMR, and BPR documentation under cGMP and ICH guidelines.

Previously at Akums Drugs & Pharmaceuticals, I supported technology transfer from development through commercial production, including pilot, validation, and troubleshooting batches for tablets. I bring an M. Pharm in Pharmaceutics and experience collaborating across regulatory, analytical, manufacturing, and research teams.

Experience

Work history, roles, and key accomplishments

MSN Laboratories logoML
Current

Executive (FR&D)

Aug 2025 - Present (1 year 1 month)

• Executed end-to-end development of generic solid oral dosage forms for US (FDA), Europe (EMA), ROW and WHO markets, supporting ANDA and EU dossier submissions.
• Designed and executed pre-formulation, formulation optimization, stability studies, scale-up, and exhibit batch activities, ensuring robust technology transfer to manufacturing sites.
• Ensured full compliance with cGMP and ICH Q8/Q9/

Akums Drugs& Pharmaceuticals Ltd logoAL

Assistant Research Associate - Technology Transfer (R&D)

Oct 2023 - Jul 2025 (1 year 9 months)

• Performed different methodologies being employed for tablets mainly covering all aspects from granulation, compression, coating & Packaging.
• Involved in different product development/technology transfer batches, scale-up batches & process validation batches of MNCs for Indian market.
• Executes Pilot batches/validation batches, Reprocess Trials and troubleshooting of production batches and e

FDA logoFD

Internship Trainee

Jan 2020 - Feb 2020 (1 month)

Internship trainee at FDA.

Education

Degrees, certifications, and relevant coursework

Rajiv Gandhi Proudyogiki Vishwavidyalaya logoRV

Rajiv Gandhi Proudyogiki Vishwavidyalaya

Master of Pharmacy, Pharmaceutical Sciences

2020 - 2022

Master's degree in Pharmaceutical Sciences from Rajiv Gandhi Proudyogiki Vishwavidyalaya from 2020 to 2022.

Rajiv Gandhi Proudyogiki Vishwavidyalaya logoRV

Rajiv Gandhi Proudyogiki Vishwavidyalaya

Bachelor of Pharmacy, Pharmacy

2016 - 2020

Bachelor of Pharmacy from Rajiv Gandhi Proudyogiki Vishwavidyalaya from 2016 to 2020.

Tech stack

Software and tools used professionally

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