API RD AD Regulatory Affairs Jobs in Gujarat at BDR Pharmaceuticals professionals walk-in February 2026
Advance Your Career in API Research & Regulatory Affairs – Walk-In Drive in Vadodara
Experienced pharmaceutical professionals seeking growth in API research, analytical sciences, or regulatory affairs now have a promising opportunity in Gujarat. BDR Pharmaceuticals International Pvt. Ltd. is conducting a walk-in interview for multiple technical and regulatory roles at its Luna manufacturing plant near Vadodara. API RD AD Regulatory Affairs Jobs in Gujarat
Candidates with 2 to 12 years of experience in API R&D, analytical method development, impurity profiling, or regulatory documentation are invited to attend the interview and explore career opportunities in a USFDA-compliant manufacturing environment. API RD AD Regulatory Affairs Jobs in Gujarat
Company Overview
BDR Pharmaceuticals International Pvt. Ltd. is a recognized pharmaceutical organization engaged in the development and manufacturing of Active Pharmaceutical Ingredients (APIs), peptides, and complex generics for regulated markets. The company operates advanced facilities in Gujarat and focuses on high-quality production aligned with global regulatory requirements.
With a strong presence in therapeutic segments such as oncology, cardiology, and anti-diabetic formulations, BDR emphasizes innovation, compliance, and research-driven manufacturing. Its facilities are approved by major regulatory authorities, including the USFDA, making it a preferred employer for professionals seeking international exposure. API RD AD Regulatory Affairs Jobs in Gujarat
Job Location & Employment Type
- Company: BDR Pharmaceuticals International Pvt. Ltd.
- Plant Location: Luna, Near Vadodara, Gujarat
- Employment Type: Full-Time
- Experience Required: 2–12 years
- Hiring Mode: Walk-In Interview
Selected candidates will be placed at the company’s Luna manufacturing and R&D facility. API RD AD Regulatory Affairs Jobs in Gujarat
Open Positions / Department Details
BDR Pharmaceuticals is recruiting for multiple roles across the following departments:
1. API Research & Development (R&D)
- API Synthesis – 2 to 4 years
- Peptide Synthesis – 2 to 4 years
- Process Development Laboratory – 2 to 4 years
- Impurities Research – 2 to 4 years
- Polymorphism Studies – 2 to 4 years
2. Regulatory Affairs (API)
- Regulatory Affairs (API) – 4 to 11 years
3. Analytical Development & Impurities (ADL)
- Analytical Method Validation (LCMS) – 4 to 5 years
- Analytical Method Development & QMS – Around 2+ years
- Analytical Synthesis Method Validation & QMS – 9 to 12 years
Preference will be given to candidates with experience in regulated markets such as the US and EU, especially those who have worked in USFDA-approved facilities.
Key Roles & Responsibilities
API R&D Roles
- Develop and optimize synthetic routes for APIs and intermediates.
- Perform scale-up studies and process optimization.
- Conduct peptide synthesis and related research activities.
- Carry out impurity profiling and characterization.
- Execute polymorphism studies and stability assessments.
- Maintain laboratory documentation as per cGMP and ICH guidelines.
Analytical Development Roles
- Develop and validate analytical methods using HPLC, LCMS, GC, and related instruments.
- Perform analytical method troubleshooting and validation.
- Conduct impurity analysis and stability testing.
- Maintain laboratory compliance under GLP standards.
- Ensure adherence to Quality Management Systems (QMS).
Regulatory Affairs (API)
- Prepare and review regulatory submissions for international markets.
- Compile documentation for DMF filings and other regulatory dossiers.
- Coordinate with R&D and analytical teams for data compilation.
- Ensure compliance with USFDA, ICH, and other global regulatory standards.
- Support regulatory audits and inspections.
API RD AD Regulatory Affairs Jobs in Gujarat
Eligibility Criteria
Education
- M.Sc / M.Pharm / Ph.D in Organic Chemistry, Pharmaceutical Chemistry, Analytical Chemistry, or related disciplines.
Degrees must be obtained from recognized universities or institutions.
Experience
- Entry-Level Technical Roles: 2–4 years
- Mid-Level Analytical/Regulatory Roles: 4–8 years
- Senior/Managerial Technical Roles: 9–12 years
Experience in API manufacturing and regulated market exposure is strongly preferred. API RD AD Regulatory Affairs Jobs in Gujarat
Skills Required
- Strong knowledge of synthetic chemistry and process development.
- Expertise in analytical instruments such as HPLC, LCMS, and GC.
- Understanding of impurity profiling and polymorphism studies.
- Familiarity with cGMP, GLP, ICH, and USFDA regulatory requirements.
- Experience in regulatory dossier preparation (for RA roles).
- Strong documentation, data analysis, and problem-solving skills.
- Ability to work collaboratively in cross-functional R&D teams.
API RD AD Regulatory Affairs Jobs in Gujarat
Salary & Benefits
Compensation will be based on experience, designation, and technical expertise.
Typical industry salary ranges in Gujarat API companies:
- Officer / Senior Officer (2–5 years): ₹4 – 8 LPA
- Executive / Assistant Manager (4–8 years): ₹6 – 12 LPA
- Manager-Level (9+ years): ₹12 – 20+ LPA
Additional benefits may include:
- Health insurance coverage
- Provident Fund (PF)
- Performance-based incentives
- Transport facilities (plant-specific)
- Professional development opportunities
- Exposure to USFDA-regulated operations
Final salary will be discussed during the interview process.
Selection Process
The hiring process will include:
- Document verification
- Technical evaluation/interview
- HR discussion
- Final selection based on skill alignment and experience
Candidates should be prepared for in-depth technical discussions related to their area of expertise. API RD AD Regulatory Affairs Jobs in Gujarat
Walk-In Interview Details
- Date: 14th February 2026 (Saturday)
- Time: 10:00 AM to 4:00 PM
- Venue:
BDR Lifesciences Pvt. Ltd.
RS No. 578 & 579, Near Effluent Channel Road,
Village: Luna, Taluka: Padra,
District: Vadodara – 391440, Gujarat
Contact Person: Mrunal Uttekar
Email: mrunal.uttkar@bdrpharma.com
Documents to Carry
Candidates attending the walk-in interview must bring:
- Updated Resume
- Educational Certificates (Original & Copies)
- Experience Letters
- Recent Passport-Size Photographs
Ensure all documents are properly organized for verification.
Why Apply for This Pharma Job?
- Opportunity to work in a USFDA-approved API manufacturing facility.
- Exposure to regulated markets (US/EU).
- Career growth in R&D, Analytical Development, and Regulatory Affairs.
- Involvement in complex generics and advanced research projects.
- Competitive salary aligned with Gujarat pharma industry standards.
- Professional environment focused on innovation and compliance.
This recruitment drive is ideal for professionals looking to build or strengthen their careers in API research and international regulatory operations. API RD AD Regulatory Affairs Jobs in Gujarat
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform that provides pharmaceutical industry job updates. We are not affiliated with BDR Pharmaceuticals International Pvt. Ltd. or any other organization mentioned above. Candidates are advised to verify official details directly with the company before proceeding. API RD AD Regulatory Affairs Jobs in Gujarat
Final Call-to-Action
If you have relevant experience in API R&D, analytical sciences, or regulatory affairs and are seeking growth in a regulated pharmaceutical environment, attend the walk-in interview at BDR Pharmaceuticals on 14th February 2026 and take the next step in your professional journey. API RD AD Regulatory Affairs Jobs in Gujarat
