Gowrie Research Walk-in RA, F&D, ADL
- Company Overview
- Walk-In Interview Details
- Job Role & Responsibilities
- 1. F&D – Officer / Sr. Officer
- 2. ADL – Research Associate / Sr. Research Associate
- 3. ADL (Special Product) – Sr. Research Associate
- 4. Project Management – Sr. Officer / Executive
- 5. Trainee (Fresher Role)
- 6. Regulatory Affairs (Pharmacology) – Team Leader / Asst. Manager
- 7. RA (PLPI) – Freshers
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Build a Career in Regulatory Affairs & F&D?
- Frequently Asked Questions (FAQs)
- 1. How many total vacancies are available?
- 2. Are freshers eligible?
- 3. What is the walk-in schedule?
- 4. Is M.Pharm mandatory for all roles?
- 5. Can candidates apply by email?
- Job Summary
MPharm RA F&D ADL Jobs Vadodara
M.Pharm/M.Sc RA, F&D, ADL vacancies (10 posts) at B&S Group Vadodara. Walk-in 09–13 Mar 2026.
B&S Group (UK-based Pharma MNC) is conducting a multi-day walk-in drive for experienced and fresher professionals across F&D, ADL, Regulatory Affairs, and Project Management functions at its Vadodara facility. Candidates with M.Pharm, M.Sc, B.Pharm, and B.Sc qualifications are invited to attend between 09 March and 13 March 2026.
If you are searching for regulatory affairs jobs in Vadodara, formulation development vacancies, ADL research associate roles, pharmacology regulatory careers, or M.Pharm jobs in pharma MNCs, this hiring drive offers exposure to international regulatory standards and global pharmaceutical projects.
Company Overview
B&S Group is a UK-based pharmaceutical organization with a strong focus on formulation development, analytical research, and regulatory services for global markets. Operating through Gowrie Research Pvt. Ltd. in India, the company supports product development, regulatory submissions, pharmacovigilance documentation, and dossier management for regulated territories.
The Vadodara unit plays a key role in:
- Formulation & Development (F&D)
- Analytical Development Laboratory (ADL)
- Regulatory Affairs (EU/UK market focus)
- Project Management for product lifecycle execution
Working with a global pharmaceutical MNC environment provides professionals with exposure to international regulatory frameworks, CTD dossier preparation, product lifecycle management, and advanced analytical development practices.
Walk-In Interview Details
Walk-In Dates: 09 March 2026 – 13 March 2026 (Monday to Friday)
Time: 11:00 AM – 07:30 PM
Venue:
B&S Group – Gowrie Research Pvt. Ltd.
No. 2, BP Estate, NH No. 8
Near Prakruti Resort, Chhani
Vadodara – 391740, Gujarat
Candidates may also email their CV to:
jobs@bnsgroup.co.uk
Job Role & Responsibilities
1. F&D – Officer / Sr. Officer
Qualification: M.Pharm
Experience: 2–4 Years
Vacancy: 01
Key Responsibilities:
- Support formulation development activities
- Conduct literature review and product development planning
- Prepare development reports and technical documentation
- Coordinate with ADL and regulatory teams for product submissions
Strong understanding of pharmaceutical formulation principles and regulatory requirements is required.
2. ADL – Research Associate / Sr. Research Associate
Qualification: M.Sc / B.Pharm / M.Pharm
Experience: 3–8 Years
Vacancies: 03
Key Responsibilities:
- Perform analytical method development and validation
- Handle HPLC and other analytical instruments
- Prepare analytical reports and stability data documentation
- Ensure compliance with GMP and data integrity standards
3. ADL (Special Product) – Sr. Research Associate
Qualification: M.Pharm
Experience: 8–10 Years
Vacancy: 01
Key Responsibilities:
- Lead analytical development for complex or special products
- Design validation protocols and analytical strategies
- Support regulatory submission documentation
- Mentor junior analytical team members
4. Project Management – Sr. Officer / Executive
Qualification: M.Pharm
Experience: 3–5 Years
Vacancy: 01
Key Responsibilities:
- Coordinate cross-functional project timelines
- Track development milestones and regulatory submissions
- Prepare project status reports and risk assessments
- Ensure adherence to global regulatory timelines
5. Trainee (Fresher Role)
Qualification: M.Sc / B.Sc
Experience: 0–1 Year
Vacancy: 01
Key Responsibilities:
- Assist in laboratory documentation and sample handling
- Support research and regulatory documentation tasks
- Maintain data accuracy and record keeping
6. Regulatory Affairs (Pharmacology) – Team Leader / Asst. Manager
Qualification: M.Pharm
Experience: 10–13 Years
Vacancy: 01
Key Responsibilities:
- Lead regulatory submission strategies
- Review CTD/eCTD dossiers for regulated markets
- Manage pharmacology-related documentation
- Coordinate with international regulatory authorities
7. RA (PLPI) – Freshers
Qualification: M.Sc / B.Sc
Experience: 0–1 Year
Vacancies: 03
Key Responsibilities:
- Assist in preparation of Patient Leaflet & Product Information (PLPI) documents
- Support regulatory document formatting and compliance checks
- Work under supervision for submission documentation
Eligibility / Qualifications
Relevant Courses (comma-separated):
M.Pharm (Pharmaceutics, Pharmaceutical Analysis, Pharmacology), B.Pharm, M.Sc Chemistry, M.Sc Life Sciences, B.Sc Life Sciences
Experience Range:
0–13 Years (Role Dependent)
Industry Background: Pharmaceutical formulation development, analytical development, regulatory affairs, or project management preferred.
Location & Salary
Work Location: Vadodara, Gujarat
Industry: Pharmaceutical R&D, Regulatory Affairs, Analytical Development
Vadodara is a growing pharmaceutical and regulatory services hub with strong demand for regulatory affairs professionals and formulation scientists.
Salary: Compensation will be offered as per industry standards and experience level. Senior regulatory and analytical roles typically attract competitive salary packages aligned with global market exposure.
Application Process
Candidates can attend the walk-in between 09–13 March 2026.
Alternatively, send your updated CV to:
jobs@bnsgroup.co.uk
Documents to Carry:
- Updated Resume
- Educational Certificates
- Experience Certificates
- Last Salary Details (if applicable)
Shortlisted candidates will be evaluated through technical and HR interviews.
Why Build a Career in Regulatory Affairs & F&D?
Regulatory Affairs and Analytical Development roles offer:
- Global market exposure (UK/EU regulations)
- Strong career growth in pharmaceutical compliance
- High demand skills in dossier preparation and CTD submissions
- Exposure to lifecycle management and product launches
- Competitive salary growth in pharma regulatory domain
Professionals trained in regulatory and analytical roles within international MNC environments are highly valued in the pharmaceutical industry.
Frequently Asked Questions (FAQs)
1. How many total vacancies are available?
A total of 10 positions across F&D, ADL, RA, and Project Management.
2. Are freshers eligible?
Yes, freshers are eligible for Trainee and RA (PLPI) roles.
3. What is the walk-in schedule?
09–13 March 2026, 11:00 AM to 07:30 PM.
4. Is M.Pharm mandatory for all roles?
M.Pharm is required for senior F&D and RA leadership roles. Other positions accept M.Sc/B.Sc/B.Pharm.
5. Can candidates apply by email?
Yes, resumes can be emailed to jobs@bnsgroup.co.uk.
Job Summary
| Company | B&S Group (Gowrie Research Pvt. Ltd.) |
|---|---|
| Vacancies | F&D Officer; ADL Research Associate; Sr RA; Project Mgmt; Trainee; RA PLPI |
| Required Education | M.Pharm, B.Pharm, M.Sc, B.Sc |
| Experience | 0–13 Years (Role Based) |
To apply for this job email your details to jobs@bnsgroup.co.uk
