Gowrie Research Hiring R&D, Regulatory Affairs, ADL & IPR
- Company Overview
- Job Role & Responsibilities
- Formulation & Development (F&D)
- Regulatory Affairs – UK & EU Markets
- Regulatory Affairs (PLPI)
- Analytical Development (ADL)
- Intellectual Property Rights (IPR)
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Summary Table
M.Pharm/B.Pharm R&D & Regulatory Vacancies – Vadodara
Gowrie Research hiring for R&D, Regulatory Affairs, ADL & IPR roles in Vadodara. Multiple vacancies for B.Pharm/M.Pharm/M.Sc candidates.
Gowrie Research Pvt. Ltd. is expanding its R&D and Regulatory Affairs teams and is inviting skilled pharmaceutical professionals to join its Vadodara operations. This opportunity suits candidates experienced in formulation development, analytical science, regulatory submissions, and intellectual property management across global markets.
Company Overview
Gowrie Research Pvt. Ltd., formerly Thame Laboratories Licensed Medicines Division, is a well-established pharmaceutical organisation with a strong presence in the UK and EU markets. The company specialises in developing, licensing, and manufacturing high-quality liquid medicines and holds more than 50 approved marketing authorisations.
Job Role & Responsibilities
Formulation & Development (F&D)
- Lead development activities for complex liquid formulations.
- Manage end-to-end formulation design, trials, optimisation and documentation.
- Ensure regulatory compliance across UK/EU guidelines.
Regulatory Affairs – UK & EU Markets
- Prepare and review regulatory dossiers.
- Manage submissions for product approvals in regulated markets.
- Coordinate with cross-functional teams for documentation and compliance.
Regulatory Affairs (PLPI)
- Support PLPI regulatory documentation.
- Assist in technical file preparation and data coordination.
Analytical Development (ADL)
- Conduct analytical method development and validation.
- Perform routine analysis using HPLC, GC and other instruments.
- Maintain compliance with GLP and data integrity standards.
Intellectual Property Rights (IPR)
- Support patent drafting and literature searches.
- Maintain IP documentation and coordinate with legal/technical teams.
Eligibility / Qualifications
- F&D (Research Scientist/Sr. Scientist): M.Pharm with 6–8 years’ experience.
- Regulatory Affairs (UK/EU): B.Pharm/M.Pharm with 6–8 years’ experience.
- Regulatory Affairs PLPI (Trainee): B.Sc/M.Sc/B.Pharm, 0–1 year (freshers eligible).
- Analytical Development (ADL): B.Sc/M.Sc/B.Pharm with 1–3 years’ experience.
- IPR: B.Pharm/M.Pharm with 1–3 years’ experience.
Relevant Courses: B.Pharm, M.Pharm (Pharmaceutics, Quality Assurance, Regulatory Affairs), B.Sc Chemistry, M.Sc Chemistry, Pharmaceutical Analysis.
Location & Salary
- Location: BP Estate, N.H. No.8, Chhani, Vadodara – 391740.
- Salary as per industry standards; based on experience.
Application Process
Interested candidates can attend the walk-in drive or share their updated resume via email.
- Walk-in Dates: 1st to 5th December 2025
- Time: 11:00 AM to 08:00 PM
- Emails: jobs@bnsgroup.co.uk, darshan.joshi@bnsthamelabs.com
- Contact: 98985 68926 / 6358219388
- Website: www.syrimed.co.uk
Summary Table
| Category | Details |
|---|---|
| Company | Gowrie Research Pvt. Ltd. |
| Vacancies | F&D, RA (UK/EU), RA PLPI, ADL, IPR |
| Required Education | B.Pharm, M.Pharm, B.Sc, M.Sc |
| Experience | 0–8 years depending on role |
To apply for this job email your details to darshan.joshi@bnsthamelabs.com
