BDR Pharmaceuticals Walk-In Drive 2026: Multiple Openings in Regulatory Affairs (RA) & Analytical Development Laboratory (ADL)

BDR Group of Companies—a prominent manufacturer specializing in active pharmaceutical ingredients (APIs) and advanced finished dosage formulations—has announced an open walk-in recruitment interview drive at Vadodara, Gujarat. Experienced pharmaceutical professionals are invited to apply for critical openings across its Regulatory Affairs and Analytical Development Laboratory divisions.

Walk-In Drive Schedule & Venue

Date: Sunday, 27 September 2026
Venue:201–203 Lotus Plaza,Near Vishanti Heritage Bungalow,30 MT Road, Gotri,Vadodara – 390021, Gujarat

Division & Position Breakdowns

1. Regulatory Affairs (RA) – Gotri Location

RA – US Market (Executive / Senior Executive)
- Experience: Up to 8 years in CMC (Chemistry, Manufacturing, and Controls) aspects.
- Core Scope: Preparation, compilation, and review of regulatory dossiers (ANDA, NDA, variations, renewals) in eCTD and non-eCTD formats for US and EU markets; addressing health authority queries (FDA, EMA, ANVISA, Health Canada, TGA); post-approval labeling updates, variations, and database maintenance.
RA – Rest of World (ROW) Market (Officer / Executive)
- Core Scope: Multi-country dossier compilation conforming to international regulatory frameworks; routine lifecycle activities (submissions, renewals, variations); regulatory query management and cross-functional coordination (R&D, QA, QC, Production).

2. Analytical Development Laboratory (ADL) – Baska Location

ADL – Query & Characterization
- Core Scope: Advanced analytical method development, optimization, and troubleshooting for complex dosage forms (lyophilized products, injectables, depot formulations, peptides, and oral solids) following Quality by Design (QbD) principles; handling regulatory queries; conducting advanced instrumental characterization utilizing DSC, XRD, NMR, FT-IR, HPLC, and LC-MS.
ADL – Documentation Review
- Core Scope: Drafting and reviewing analytical specifications, Standard Test Procedures (STP/MOA) for raw materials, in-process, and finished products; vendor qualification and tech transfer documentation; maintaining records for microbiological, chemical, and residual solvent data; routine calibration and lab standard management.
ADL – Manufacturing Science & Technology (MS&T)
- Core Scope: Leading analytical method transfers from R&D/ADL to QC laboratories and manufacturing sites; drafting Tech Transfer Protocols (TTP) and validation reports; analytical method validation, verification, and troubleshooting compliant with ICH and cGMP guidelines.

Candidate Checkpoints

Documents Required: Candidates must attend the walk-in interview with an updated CV/resume, recent passport-size photograph, academic records, latest CTC/increment letter, and previous 3 months’ pay slips.