Research Associate / Senior Research Associate - Analytical Development Laboratory (ADL)

Why This Role Matters

Analytical Development plays a critical role in pharmaceutical product lifecycle management. From method development and validation to stability data interpretation, the Analytical Development Laboratory (ADL) ensures product quality, regulatory compliance, and scientific integrity.

This Walk-In Drive, organized by Gowrie Research Pvt. Ltd. under B&S Group, is a dedicated hiring initiative for women professionals, offering growth opportunities in R&D and regulatory-focused domains.

The ADL team supports formulation development, scale-up activities, and regulatory submissions by generating scientifically sound analytical data. Professionals joining this function contribute directly to quality assurance, regulatory acceptance, and successful product commercialization.

Job Description

B&S Group – Gowrie Research Pvt. Ltd., Vadodara, is conducting a Walk-In Drive for Women Professionals from 23rd to 27th February 2026. The organization is hiring experienced candidates for the Analytical Development Laboratory (ADL) across standard and special product segments.

The selected candidates will be responsible for analytical method development, validation, stability studies, instrument handling, and regulatory documentation support. The role requires strong technical knowledge, regulatory awareness, and the ability to work in a structured R&D environment.

Key Features of the Role

• Direct involvement in analytical method development and validation
• Exposure to regulated market documentation standards
• Hands-on experience with advanced analytical instruments
• Opportunity to work on special product development projects
• Participation in stability studies and data interpretation
• Women-focused hiring initiative promoting leadership and growth
• Strong career pathway in R&D and regulatory compliance

Responsibilities Required

Analytical Method Development & Validation

• Develop and optimize analytical methods for pharmaceutical formulations
• Perform method validation as per ICH guidelines
• Ensure accuracy, precision, robustness, and reproducibility of analytical methods
• Prepare validation protocols and reports
• Troubleshoot analytical challenges and provide scientific solutions

Stability Studies & Data Analysis

• Conduct stability studies as per regulatory requirements
• Analyze stability samples and interpret data trends
• Identify out-of-specification (OOS) or out-of-trend (OOT) results
• Support stability report preparation and documentation
• Collaborate with formulation teams for stability improvements

Instrument Handling & Laboratory Operations

• Operate and maintain analytical instruments such as HPLC, GC, UV-Visible Spectrophotometer, and related equipment
• Perform system suitability testing and calibration checks
• Maintain proper documentation and ensure data integrity
• Follow laboratory safety and GMP practices
• Ensure proper maintenance of analytical records

Regulatory Documentation Support

• Prepare analytical sections for regulatory submissions
• Support dossier compilation for regulated and semi-regulated markets
• Maintain documentation aligned with GMP and data integrity standards
• Assist during audits and regulatory inspections
• Coordinate with QA and regulatory teams for compliance verification

Special Products (Senior Role)

• Lead analytical activities for complex or special product portfolios
• Provide technical guidance to junior team members
• Oversee method transfer and cross-functional coordination
• Support strategic R&D initiatives
• Drive continuous improvement in analytical processes

Qualifications

Candidates must possess strong analytical expertise, regulatory understanding, and laboratory discipline. The role demands scientific accuracy, documentation excellence, and problem-solving ability.

For senior-level positions, leadership capability and experience handling complex projects are essential.

Educational Requirements

Research Associate / Sr. Research Associate – ADL
• M.Sc/ B.Pharm / M.Pharm

Senior Research Associate – ADL (Special Products)
• M.Pharm (Mandatory)

Specialization in Pharmaceutical Analysis or related discipline preferred.

Experience and Skills

Experience

• 3–8 years for Research Associate / Sr. Research Associate
• 8–10 years for Special Products Senior Role
• Experience in regulated market exposure preferred

Technical Skills

• Strong knowledge of analytical method development
• Experience in method validation as per ICH guidelines
• Stability study execution and interpretation
• Hands-on experience with HPLC, GC, UV, and related instruments
• Knowledge of GMP and data integrity requirements
• Familiarity with regulatory documentation standards

Behavioral Skills

• Strong analytical and troubleshooting skills
• Detail-oriented documentation practices
• Ability to manage multiple projects
• Effective communication and collaboration
• Leadership capability (for senior roles)
• Proactive and quality-focused mindset

Salary Insights

• Estimated salary range (3–8 years experience): ₹5 LPA – ₹9 LPA
• Estimated salary range (8–10 years senior role): ₹9 LPA – ₹14 LPA
• Compensation may vary depending on expertise in special products and regulatory exposure
• Performance-based incentives may be applicable

Additional Benefits

• Performance-based incentives
• Professional growth in R&D and regulatory domains
• Exposure to special product development projects
• Women-focused empowerment hiring initiative
• Opportunity to work in structured, compliance-driven environment

Company Overview

Gowrie Research Pvt. Ltd., part of B&S Group, is a pharmaceutical research-driven organization specializing in formulation development, analytical research, quality systems, and regulatory-focused operations.

Located in Vadodara, the organization emphasizes scientific innovation, regulatory excellence, and operational quality. It provides strong career growth opportunities in R&D, QA, and project management domains, especially for professionals seeking exposure to regulated market standards.

Walk-In & Application Process

Walk-In Dates: 23rd to 27th February 2026
Location: Vadodara

Interested candidates should:

• Attend the walk-in interview during the specified dates
• Carry updated resume and educational documents
• Reach early due to limited vacancies

FAQs

1. Is this walk-in drive only for women professionals?
   Yes, this is a dedicated hiring initiative for women professionals.

2. Is regulated market experience required?
   Preferred but not mandatory for mid-level roles; highly desirable for senior positions.

3. What instruments experience is required?
   Hands-on experience with HPLC, GC, UV, and similar analytical instruments.

4. Are freshers eligible?
   No, relevant experience is required for these roles.

5. Is leadership experience required for the senior role?
   Yes, the Special Products Senior role requires leadership and advanced analytical expertise.

Application Tips

• Clearly mention analytical instruments handled
• Highlight method validation and stability study experience
• Include regulatory submission exposure
• Quantify number of methods developed or validated
• Mention experience in special or complex product handling
• Carry all academic and experience certificates during walk-in

This walk-in opportunity is ideal for experienced women professionals looking to advance their careers in Analytical Development and regulated pharmaceutical research domains.