Sun Pharma: Hiring Senior Executive — MS&T (Orals)

Sun Pharmaceutical Industries Ltd. is hiring an experienced professional for the position of Senior Executive in the Manufacturing Science and Technology (MS&T) – Orals department at their Halol facility.

Key Job Details

• Company: Sun Pharmaceutical Industries Ltd.
• Function / Department: MS&T – Orals
• Grade / Designation: Senior Executive
• Qualification: M. Pharm
• Experience Required: 8 to 10 Years of relevant experience
• Job Location: Halol, Gujarat

Key Responsibilities & Scope of Work

• Project Management: Lead Exhibit Projects, New Launch Projects, Troubleshooting Projects, and Product Life Cycle Projects.
• Cross-Functional Coordination: Coordinate seamlessly with Formulation Development, Production, Engineering, QC, QA, Packaging, and other departments to ensure timely project execution.
• Batch Execution & Monitoring: Plan, track, and monitor trial batches, scale-up batches, exhibit batches, and commercial/PV batches.
• Technical Documentation:
  • Prepare and review Trial Batch Objectives, BMRs, Protocols, Reports, Technical Reports, and Regulatory Query Responses.
  • Draft and verify core documents including BMR, BOM, MFC, MF, and study protocols.
• Technical Support & Troubleshooting: Support Cross-Functional Teams (CFTs) in troubleshooting production/QA/QC issues during trial, scale-up, and exhibit batch manufacturing.
• R&D & Lifecycle Management: Conduct trials/evaluations at R&D for hypothesis testing, troubleshooting, and product lifecycle management.
• SAP Management: Execute SAP-related activities such as recipe preparation/approval, process order preparation/release, sample management, and related tasks.

📩 Direct E-mail Application Channel

Interested candidates with relevant experience in MS&T (Orals) can share their updated resume directly with the HR team:

• 📧 Direct HR Email: Rosemary.varghese@sunpharma.com
• 📌 Subject Line Format: Application for Sr. Executive MS&T (Orals) - [Years of Experience] - [Current Location] - [Your Name]

NATCO Pharma: Walk-In Interview for Production, QC & Microbiology

NATCO Pharma Limited is hosting a walk-in interview recruitment drive for experienced professionals and candidates looking to join its Production, Quality Control (QC), and Microbiology departments.

The openings are for the NATCO Formulation Division based in Kothur (near Hyderabad).

Key Job Details

• Company: NATCO Pharma Limited
• Departments: Production | Quality Control | Microbiology
• Work Location: NATCO Formulation Division, Kothur (Approx. 50 km from Hyderabad)
• Job Type: Full-Time / On-site

Department & Role Highlights

📅 Walk-In Schedule & Venue Details

📋 Mandatory Documents to Carry

Candidates attending the walk-in drive are advised to carry:

• Updated Resume / CV
• 2 Passport-size Photographs
• Original and photocopies of Educational Certificates (SSC to Degree/PG)
• Latest 3 months' Pay Slips and CTC Breakup Letter (for experienced candidates)
• Government ID Proof (Aadhaar Card / PAN Card)

Dr. Reddy's Laboratories is looking for experienced Analytical R&D Scientists to support method development and validation for complex generics and API molecules.

Key Job Details

• Company: Dr. Reddy's Laboratories Ltd.
• Role: Associate Scientist / Research Scientist — Analytical R&D
• Experience Required: 3 – 7 Years
• Work Location: Integrated Product Development Organisation (IPDO), Bachupally, Hyderabad
• Salary Package: ₹6.0 LPA – ₹11.0 LPA + Performance Bonus

Qualification & Technical Requirements

Core Responsibilities

• Develop and validate stability-indicating analytical methods in accordance with ICH guidelines (Q2R1).
• Author and review analytical method validation protocols, reports, and specification datasheets for regulatory filings (DMF / ANDA).
• Troubleshoot complex chromatographic issues and maintain strict compliance with 21 CFR Part 11 data integrity standards.

📩 Direct E-mail Application Channel

• 📧 Direct HR Email: ard.talent@drreddys.com
• 📌 Subject Line Format: AR&D Scientist - [Years of Exp] - [Current Company] - [Your Name]
  • Example: AR&D Scientist - 5 Years - Cipla Ltd - Srikant Verma

Sun Pharma: Hiring for Senior Executive / Assistant Manager — Quality Assurance (QA)

Sun Pharmaceutical Industries Ltd. is recruiting experienced Quality Assurance professionals for its sterile manufacturing and formulation facilities.

Key Job Details

• Company: Sun Pharmaceutical Industries Ltd.
• Role: Senior Executive / Assistant Manager — Quality Assurance (QA)
• Experience Required: 4 – 8 Years
• Work Location: Halol (Gujarat) / Paonta Sahib (Himachal Pradesh)
• Salary Package: ₹6.5 LPA – ₹10.5 LPA (Depending on current CTC and experience)

Experience & Competency Framework

Core Responsibilities

• Lead IPQA teams on production lines, ensuring strict compliance with cGMP guidelines and site SOPs.
• Drive risk assessment studies and execute root cause analysis (RCA) for batch failures and market complaints.
• Review and approve Master Batch Production Records (MBPR), Process Validation protocols, and Cleaning Validation reports.

📩 Direct E-mail Application Channel

• 📧 Direct HR Email: quality.careers@sunpharma.com
• 📌 Subject Line Format: Application for Sr. Exec QA - [Years of Exp] - [Current Location] - [Your Name]
  • Example: Application for Sr. Exec QA - 6 Years - Vadodara 

Cognizant: Walk-In Drive & Hiring for Medical Coding Freshers

Cognizant Technology Solutions is recruiting fresh B.Pharm, Pharm.D, B.Sc, M.Sc (Life Sciences), and Allied Health graduates for the position of Medical Coder (Trainee) in its Healthcare & Life Sciences division.

This role involves translating medical records, doctor diagnoses, and procedure notes into standardized alphanumeric codes used globally in healthcare billing and clinical research.

Key Job Details

• Company: Cognizant Technology Solutions
• Role: Junior Medical Coder / Medical Coding Trainee
• Target Audience: Freshers (0 – 1 Year Experience / 2024, 2025, 2026 Batches)
• Work Location: Hyderabad, Chennai, or Coimbatore (On-site / Rotational Shifts)
• Salary Package: ₹2.8 LPA – ₹3.8 LPA + Night Shift Allowances & Health Insurance

Department Breakdown & Eligibility Criteria

Core Responsibilities

• Medical Chart Review: Read and analyze physician clinical notes, outpatient records, and diagnostic procedures.
• Code Assignment: Assign accurate diagnostic and procedural codes using standard code sets (ICD-10-CM, CPT, and HCPCS).
• Quality & Compliance: Maintain high accuracy standards (above 95%) to prevent claim rejections and ensure compliance with HIPAA and US healthcare guidelines.

📅 Walk-In Schedule & Direct Application Details

📩 Direct E-mail Application Channel

Candidates who are unable to attend the venue in person can submit their CV directly to the Cognizant Healthcare Talent Acquisition desk:

• 📧 Direct HR Email: healthcare.careers@cognizant.com
• 📌 Subject Line Format: Medical Coder Trainee - [Qualification] - [Passing Year] - [Your Name]
  • Example: Medical Coder Trainee - B.Pharm - 2025 - Sneha Reddy

IQVIA: Off-Campus Hiring for Clinical Data Management (CDM) Freshers

IQVIA—a global leader in clinical research, advanced analytics, and healthcare technology—is recruiting fresh B.Pharm, Pharm.D, B.Sc, and M.Sc (Life Sciences) graduates for entry-level Clinical Data Associate / Data Management Trainee positions.

This role provides an opportunity to work on international clinical trials, electronic data capture (EDC) systems, and clinical data validation for global pharma sponsors.

Key Job Details

• Company: IQVIA India
• Role: Clinical Data Associate (CDM Trainee)
• Target Audience: Freshers (0 – 1 Year Experience / 2024, 2025, 2026 Batches)
• Work Location: Bengaluru, Kochi, or Hyderabad (Hybrid Work Model)
• Salary Package: ₹3.6 LPA – ₹4.8 LPA + Medical Benefits & Performance Bonus

Department Breakdown & Eligibility Criteria

Core Responsibilities

• CRF & Data Review: Perform entry and validation of clinical trial data submitted by global investigator sites.
• Discrepancy Management: Identify missing data, logic check errors, and protocol deviations; issue data queries to clinical sites for resolution.
• Database Quality Checks: Participate in user acceptance testing (UAT) for eCRF setups and support locks of clinical databases prior to statistical analysis.

📩 Direct E-mail & Application Details

Eligible candidates can submit their resume directly to the IQVIA Clinical Data Management hiring team:

• 📧 Direct HR Email: cdm.careers.india@iqvia.com
• 📌 Subject Line Format: Application for CDM Associate - [Qualification] - [Passing Year] - [Your Name]
  • Example: Application for CDM Associate - B.Pharm - 2025 - Rohan Verma