Lupin Recruitment 2026: Urgent Openings for QA Validation, QC & Apprentice Roles | Apply on Jobengine20

Lupin Limited, a global pharmaceutical leader, has announced recruitment openings across its key manufacturing and technical centers. They are actively hiring for Quality Assurance (Qualification & Validation), Quality Control (QC), and Regulatory Affairs departments.

Explore the complete vacancy details, eligibility criteria, and application procedure below to apply.

📌 Quick Job Overview

💼 Role-Wise Specifications & Responsibilities

1. Quality Assurance – Qualification & Validation Officer

• Education: B.Pharm / M.Pharm
• Experience: 2 – 5 Years
• Location: Mandideep, Bhopal (MP)
• Key Responsibilities:
  • Prepare and execute qualification and validation protocols for equipment, HVAC, water systems, and compressed air.
  • Maintain the Validation Master Plan (VMP) and oversee requalification/revalidation planners.
  • Handle Computer System Validation (CSV) protocols, deviations, CAPA, and Change Control through QMS software.

2. Quality Control (QC Officer)

• Education: B.Pharm / M.Pharm / M.Sc (Chemistry)
• Experience: 2 – 4 Years
• Location: Pithampur, MP
• Key Responsibilities:
  • Perform routine analysis of raw materials, finished products, and stability samples using HPLC, GC, UV Spectrophotometers, and Dissolution apparatus.
  • Adhere strictly to ALCOA principles for electronic data integrity and Good Documentation Practices (GDP).
  • Maintain stability chambers and track stability sample testing schedules.

3. Apprentice Trainees (QC & Regulatory Affairs)

• Education: Fresh B.Sc / B.Pharm / M.Sc
• Experience: Freshers (2024, 2025, 2026 Passed Out)
• Location: Multiple Plant Locations
• Key Responsibilities:
  • Hands-on training on analytical techniques, documentation standards, and regulatory submission processing.

📑 Required Checklist for Candidates

• Updated CV / Resume detailing core equipment and regulatory skills.
• Academic Certificates & Transcripts (10th to Highest Degree).
• Relieving Letter & Salary Slips from last employer (if experienced).
• Aadhaar & PAN Card copies.

📩 How to Apply via Jobengine20

1. Email CV to HR: Forward your updated resume directly to surajvishwakarma2@lupin.com with the subject line: “Application for [Role Name] - [Experience in Years] - Jobengine20”.
2. Official Portal: Apply online through Lupin’s career portal at jobs.lupin.com.

🚨 Disclaimer & Security Alert: Lupin Limited does not charge any monetary fee or demand security deposits during any phase of its recruitment process. Always apply through legitimate official contacts posted on Jobengine20.

Sun Pharma Recruitment Drive 2026: Openings in Quality Control, QA & Regulatory Affairs | Apply on Jobengine20

Sun Pharmaceutical Industries Ltd. is hosting a hiring drive for its flagship manufacturing and R&D facilities. They are actively seeking qualified professionals across Quality Control (QC), Quality Assurance (QA), and Regulatory Affairs (RA).

If you are looking to advance your career with India’s largest pharmaceutical company, review the position details below and submit your application.

📌 Quick Job Overview

💼 Department-Wise Job Requirements

1. Quality Control (QC Analyst / Executive)

• Education: M.Sc (Analytical Chemistry) / B.Pharm / M.Pharm
• Experience: 2 – 6 Years
• Key Responsibilities:
  • Testing and analysis of Finished Products (FP), Raw Materials (RM), and Stability samples using HPLC, GC, UV, and IR equipment.
  • Routine maintenance and calibration of analytical instruments.
  • Adherence to cGMP, GLP, and electronic data integrity standards.

2. Quality Assurance (QA Executive)

• Education: B.Pharm / M.Pharm
• Experience: 2 – 5 Years
• Key Responsibilities:
  • Managing Quality Risk Management (QRM), Incident handling, Deviations, CAPA, and Change Control.
  • Conducting internal plant audits and ensuring line clearance across production areas.
  • Reviewing electronic Batch Manufacturing Records (eBMR) and analytical data packets.

3. Regulatory Affairs (RA Officer / Executive)

• Education: M.Pharm (Regulatory Affairs / Pharmaceutics) / B.Pharm
• Experience: 1 – 4 Years
• Key Responsibilities:
  • Preparation and submission of eCTD dossiers for USFDA, EMA, and ROW markets.
  • Handling regulatory queries, deficiency letters, and lifecycle management of approved ANDAs/NDAs.
  • Coordinating with cross-functional teams (R&D, QA, QC) to gather submission data.

📄 Required Application Documents

• Updated CV / Resume
• Educational Degrees & Transcripts
• Current Company Appointment Letter / Last Incremental Letter
• Last 3 Months' Pay Slips
• Government ID Proof (Aadhaar Card / PAN Card)

📩 How to Apply via Jobengine20

1. Email Application: Send your CV directly to hr.recruitment@sunpharma.com with the subject line: “Application for [Department] - [Total Experience] - Jobengine20”.
2. Official Portal: Apply online through the official careers portal at sunpharma.com/careers.

🚨 Fraud Notice: Sun Pharma does not charge any application or recruitment fees at any stage. Beware of fraudulent emails or agents demanding payment.

Cipla Mega Walk-In Drive 2026: Openings in Quality Control, QA & Production | Apply Now on Jobengine20

Cipla Limited is conducting a recruitment drive for its flagship manufacturing facility. They are actively hiring candidates across Quality Control (QC), Quality Assurance (QA), and Production departments.

If you are looking to advance your pharmaceutical career with a leading multinational pharma brand, check the job details below and apply today!

📌 Job Overview Table

💼 Department-Wise Job Requirements

1. Quality Control (QC Executive)

• Education: M.Sc (Analytical Chemistry) / B.Pharm / M.Pharm
• Experience: 2 – 5 Years
• Key Responsibilities:
  • Hands-on experience with HPLC, GC, UV Spectrophotometer, and Dissolution apparatus.
  • Analysis of raw materials, in-process samples, and finished dosage forms.
  • Strict adherence to cGMP, GLP, and Good Documentation Practices (GDP).

2. Quality Assurance (QA Officer)

• Education: B.Pharm / M.Pharm
• Experience: 1 – 4 Years
• Key Responsibilities:
  • Handling Quality Management Systems (QMS) including Deviations, CAPA, and Change Control.
  • In-process quality checks during manufacturing and packaging.
  • Reviewing Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).

3. Production (Production Chemist - OSD/Injectables)

• Education: B.Pharm / B.Sc (Chemistry)
• Experience: 1 – 5 Years
• Key Responsibilities:
  • Operation and supervision of Granulation, Compression, and Coating machinery.
  • Batch execution as per standard operating procedures (SOPs) and safety guidelines.
  • Yield calculation and line clearance activities.

📑 Required Documents for Interview / Application

Candidates must keep updated soft copies or physical sets of the following:

1. Updated Resume / CV
2. Highest Qualification Degree & Semester Marksheets
3. Current Employer Offer Letter / Revision Letter
4. Last 3 Months' Pay Slips & Bank Statements
5. Govt. ID Proof (Aadhaar Card / PAN Card)

📩 How to Apply via Jobengine20

1. Email Application: Send your updated CV to the official HR desk at careers@cipla.com with the subject line: “Application for [Department Name] - [Your Experience in Years]”.
2. Official Portal: Apply directly via the official careers site: careers.cipla.com.

🚨 Disclaimer & Fraud Warning: Cipla India does not charge any security deposit or recruitment fees at any stage of the hiring process. Always apply through legitimate official channels provided by Jobengine20.

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