Formulation Scientist

Hyrix; Goa; On-site; INR 900,000 - 1,200,000; Full time

Job summary

Vergo Pharma Research Laboratories in Goa is seeking an experienced Formulation Scientist (Oral Solids) to develop and optimize tablet and capsule formulations for regulated markets. Candidates with M.

Pharm and 6–9 years of relevant experience will contribute to pre-formulation studies, tech transfer, scale-up, and batch activities. The role involves preparing development reports, supporting regulatory filings for US and EU markets, and ensuring compliance with quality standards throughout the

Qualifications

• Qualification: M. Pharm (Only).
• Strong experience in Oral Solid Dosage (OSD) – Tablets & Capsules (mandatory).
• Hands-on exposure to regulated markets (US & EU).
• Good understanding of formulation development processes.

Responsibilities

• Develop and optimize formulations for oral solid dosage forms (tablets & capsules).
• Conduct pre-formulation studies and compatibility analysis.
• Handle technology transfer, scale-up, and exhibit batch activities.
• Prepare and review development reports and documentation.
• Work on regulatory filings for US & EU markets.
• Ensure compliance with quality and regulatory guidelines.

Skills

OSD tablets & capsules

Regulatory exposure US & EU

Formulation development

Education

M. Pharm

Job description

Job Title: Formulation Scientist (Oral Solids)

Company: Vergo Pharma Research Laboratories

Location: Goa

Experience: 6–9 Years

Open Positions: 2

Role Overview We are hiring experienced Formulation Scientists with strong expertise in Oral Solid Dosage (Tablets & Capsules) to join our growing formulation team. The role involves development and optimization of pharmaceutical formulations for regulated markets.

Open Positions Formulation Scientist: 3–9 Years (2 Vacancies)

Key Responsibilities

• Develop and optimize formulations for oral solid dosage forms (tablets & capsules)


• Conduct pre-formulation studies and compatibility analysis


• Handle technology transfer, scale-up, and exhibit batch activities


• Prepare and review development reports and documentation


• Work on regulatory filings for US & EU markets


• Ensure compliance with quality and regulatory guidelines

Mandatory Requirements

• Qualification: M. Pharm (Only)


• Strong experience in Oral Solid Dosage (OSD) – Tablets & Capsules (mandatory)


• Hands-on exposure to regulated markets (US & EU)


• Good understanding of formulation development processes

Interview Process

2 Rounds (Virtual)

Why Join Us

• Opportunity to work with a growing pharmaceutical R&D organization


• Exposure to international regulatory markets


• Career growth in formulation development