🏢 Dr. Reddy’s Laboratories: Walk-In Drive for QC & Production Trainees

Dr. Reddy’s Laboratories is conducting a hiring drive for fresh B.Pharm, M.Pharm, B.Sc, and M.Sc graduates to join its Quality Control (QC) and Manufacturing operations as Trainees.

Key Job Details

• Company: Dr. Reddy's Laboratories Ltd.
• Designation: Technical Trainee / Executive Trainee (QC & Production)
• Target Audience: Freshers (0 – 1 Year Experience)
• Job Location: Hyderabad (Telangana) & Pydibhimavaram (Vizag)
• Salary Range: ₹2.5 LPA – ₹3.2 LPA + Subsidized Transport & Canteen Allowance

Eligibility Criteria

Selection Process

1. Written Aptitude & Technical Test: Multiple-choice questions on chemistry/pharmacy basics, safety practices, and logical reasoning.
2. Technical Interview: Review of core academic concepts, final-year project work, and understanding of cGMP principles.
3. HR Assessment: Document verification and final discussion regarding shift rotatability.

Walk-In Details & Required Documents

• Documents to Carry: Updated Resume, 2 passport-size photographs, original and photocopies of mark sheets (SSC to Degree/PG), Aadhaar card, and PAN card.

👉 Click Here to Register on Dr. Reddy's Official Careers Portal

Hetero Drugs: Mega Walk-In Interview for QA, QC & Production

Hetero Drugs—one of India's leading API and formulation manufacturers—is hosting a mega walk-in recruitment drive for freshers interested in plant operations, quality testing, and shop-floor manufacturing.

Key Job Details

• Company: Hetero Drugs Ltd.
• Role: Junior Chemist / Production Trainee / QC Analyst
• Experience: Freshers (0 – 1 Year)
• Location: Hyderabad / Visakhapatnam (AP & Telangana Units)
• Gender Preference: Male candidates preferred for shift operations (as per plant policy).

Qualification & Requirements

• Education: B.Sc (Chemistry / Life Sciences), B.Pharm, or Diploma in Chemical Engineering.
• Passout Years: 2024, 2025, or 2026.
• Key Skills: Understanding of batch operations, chemical safety, lab testing instruments, and willingness to work in rotational shifts.

Walk-In Interview Details

• Venue: Hetero Corporate Office, Sanathnagar, Hyderabad, Telangana.
• Time: 9:30 AM to 1:30 PM.

👉 Click Here to Apply on Hetero Official Portal

🏢 1. Sun Pharma: Walk-In Drive for Production & QC Freshers

Sun Pharmaceutical Industries Ltd. is conducting a walk-in interview drive for fresh B.Pharm, M.Pharm, and B.Sc/M.Sc graduates for entry-level positions in Production, Quality Control (QC), and Quality Assurance (QA).

Key Job Details

• Company: Sun Pharmaceutical Industries Ltd.
• Role: Trainee / Executive — Production & Quality
• Target Audience: Freshers (2024 / 2025 / 2026 Batch Graduates)
• Location: Vadodara / Halol, Gujarat
• Venue: Sun Pharma R&D Centre, Akota, Vadodara

Qualification & Requirements

Walk-In Interview Details

• Date & Time: Upcoming Saturday (9:00 AM – 3:00 PM)
• Documents to Carry: Updated CV, passport-size photos, original degree certificates, and Government ID proof.

👉 Click Here to Apply / Register on Sun Pharma 

Zydus Lifesciences Is Hiring a Formulation R&D Scientist

Zydus Lifesciences Ltd., a leading innovation-driven global pharmaceutical company, is recruiting for a Formulation R&D Scientist to join its R&D center in Gujarat.

If you have a background in pharmaceutical technology, pre-formulation studies, and oral solid or injectable product development, this role puts you at the heart of developing generic and complex formulation pipelines for regulated markets.

Job Overview

• Company: Zydus Lifesciences Ltd.
• Position: Scientist / Senior Scientist — Formulation Research & Development (FR&D)
• Department: Research & Development (Formulations)
• Location: Ahmedabad / Changodar, Gujarat, India
• Role Type: Full-time

Core Responsibilities

As a Formulation R&D Scientist at Zydus, you will design, execute, and scale up novel and generic drug product formulations:

• Pre-formulation & Execution: Conduct pre-formulation assessments, drug-excipient compatibility studies, and lab-scale batch trial executions for Oral Solid Dosages (OSD) or Injectables.
• Process Optimization: Optimize process parameters for granulation, compression, coating, or sterile fill-finish operations using Quality by Design (QbD) principles.
• Technology Transfer: Coordinate with pilot plant and commercial manufacturing sites to execute technology transfer, scale-up batches, and exhibit batches for regulatory filings.
• Regulatory Documentation: Author and review formulation development reports (FDR), master formula records (MFR), stability protocols, and patent-related technical summaries.

Profile Requirements

How to Apply

You can explore active job openings and submit your application on Zydus's official recruitment network:

👉 Apply Directly on Zydus Careers Portal

(Search for "Formulation R&D" or "FR&D Scientist" under the Ahmedabad location filter to submit your resume).

Biocon Biologics Is Hiring a Regulatory Affairs Manager (Biosimilars)

Biocon Biologics, a subsidiary of Biocon Ltd. and a global leader in biosimilars development, is recruiting for a Regulatory Affairs Manager to join its Global Regulatory Operations division.

If you have experience handling biological submissions, CMC reviews, and global market approvals (Emerging Markets, GCC, or US FDA/EMA), this position offers direct exposure to advanced biopharmaceutical regulatory filings.

Job Overview

• Company: Biocon Biologics Ltd.
• Position: Regulatory Affairs Manager — Biosimilars & Biologics
• Department: Global Regulatory Affairs (GRA)
• Location: Bengaluru, Karnataka, India (On-site / Campus)
• Role Type: Full-time

Core Responsibilities

As a Regulatory Affairs Manager at Biocon Biologics, you will manage regulatory filings for biosimilars across international markets:

• Dossier Preparation & Review: Prepare, compile, and review Module 1–5 CTD/eCTD submissions for biosimilar products, clinical trial applications (CTAs), and marketing authorization applications (MAAs).
• Health Authority Queries: Coordinate with internal CMC, R&D, clinical, and quality teams to formulate scientific responses to queries raised by international regulatory agencies (GCC, ANVISA, US FDA, EMA).
• Post-Approval Support: Manage product lifecycle maintenance, including post-approval changes, site transfers, renewals, and regulatory variations.
• Compliance Tracking: Maintain regulatory submission trackers, deficiency logs, and Regulatory Information Management Systems (RIMS).

Profile Requirements

How to Apply

You can review active openings and submit your candidacy on Biocon's official talent acquisition network:

👉 Apply Directly on Biocon Careers Portal

(Search for "Regulatory Affairs Manager" or "Biosimilars" under the Bengaluru location filter to submit your application).

Glenmark Pharmaceuticals Is Hiring an Associate Manager — Pharmacovigilance

Glenmark Pharmaceuticals, an innovation-driven global pharmaceutical company, is recruiting for an Associate Manager — Pharmacovigilance to join its Drug Safety & Risk Management division.

If you have a medical or pharmaceutical background and clinical safety management experience, this role offers direct involvement in evaluating drug safety data and authoring regulatory aggregate reports for global markets.

Job Overview

• Company: Glenmark Pharmaceuticals Ltd.
• Position: Associate Manager — Pharmacovigilance (PV)
• Department: Global Clinical Safety & Pharmacovigilance
• Location: Mumbai / Mahape (Navi Mumbai), Maharashtra, India
• Role Type: Full-time

Core Responsibilities

As an Associate Manager in PV at Glenmark, you will manage case processing oversight, aggregate safety reports, and regulatory compliance across global commercialized products and clinical trials:

• Aggregate Report Writing: Lead the authoring, review, and submission of aggregate safety documents including PBRERs, PSURs, DSURs, and PADDERs.
• Signal Detection & Risk Management: Evaluate safety data signals, participate in Risk Management Plan (RMP) development, and perform benefit-risk assessments.
• ICSR Management: Oversee end-to-end processing of Individual Case Safety Reports (ICSRs), vendor audits, and quality checks on adverse event entries in safety databases (e.g., Argus Safety).
• Audit Readiness: Coordinate internal audits and health authority inspections (US FDA, EMA, CDSCO) for the pharmacovigilance department.

Profile Requirements

How to Apply

You can explore official job listings and submit your candidacy on Glenmark's official recruitment portal:

👉 Apply Directly on Glenmark Careers Portal

(Search for "Pharmacovigilance" or "Associate Manager - PV" under the Mumbai / Navi Mumbai location filter to submit your resume).