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OnsiteSenior Managerhealthtech

Senior Manager - FRD (OSD Pharma, EU GMP)

GNT Page Private LimitedAhmedabad, Gujarat, IndiaPosted 19 May 2026

Senior Manager for Formulation & Development at GNT Page Private Limited, a pharmaceutical company focused on generic oral solid dosage products. This role leads the entire product development cycle from pre-formulation through to commercial-scale technology transfer. Candidates must demonstrate deep expertise in pharmaceutical science, GMP documentation, and regulatory submissions. The position involves building and leading a team in an onsite facility in Ahmedabad.

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Experience

8-12 years

Function

Research

Work mode

Onsite, India

Company

Tier 2

What you will work on

Senior Manager for Formulation & Development at GNT Page Private Limited, a pharmaceutical company focused on generic oral solid dosage products. This role leads the entire product development cycle from pre-formulation through to commercial-scale technology transfer. Candidates must demonstrate deep expertise in pharmaceutical science, GMP documentation, and regulatory submissions. The position involves building and leading a team in an onsite facility in Ahmedabad.

TAL's take

Quality 50/1005/5 clarityTier 2 company

Standard tier-2 pharmaceutical management role with well-defined scientific responsibilities but lacks flagship brand status.

Very well-defined responsibilities, clear technical requirements, and specific domain focus on OSD and GMP.

Must haves

  • Master’s degree or PhD in Pharmacy or related discipline
  • 8–12 years of experience in formulation development
  • Experience in generic product development for oral solid dosage forms
  • Experience in GMP-regulated manufacturing environment
  • Experience with scale-up, process validation, and technology transfer

Tools and skills

pre-formulation studiesexcipient compatibilitygeneric product developmentoral solid dosage formsmanufacturing processesdissolution developmentstability studiesich stability principlespharmacopoeial requirementsctd module 3 structurequality by designfmeaprocess scale-uptechnology transfergmp documentation

Nice to have: regulated market submissions, eu-gmp, who-gmp, bioequivalence-driven development.

About the company

unfamiliar company, default mid-tier