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V-Ensure Pharma Technologies Pvt. Ltd. is conducting a Walk-In Interview Drive on 28th June 2026 (Sunday) for experienced professionals and fresh engineering graduates. The company is hiring for multiple positions across Quality Assurance, Quality Control, Production, ITQA, Engineering, Formulation Development, Analytical Research & Development, Technology Transfer, and Drug Regulatory Affairs departments.
This is an excellent opportunity to join a USFDA & EU-GMP approved OSD manufacturing facility and build a rewarding career in the pharmaceutical industry.
About V-Ensure Pharma
V-Ensure Pharma Technologies Pvt. Ltd. is a reputed pharmaceutical company engaged in the development, manufacturing, and marketing of oral solid dosage formulations for regulated markets. The company operates a world-class manufacturing facility at Additional Patalganga MIDC, Panvel, Maharashtra.
Open Positions
Quality Control / Analytical Lab
Section: Stability Studies, FP/IP, GLP & AMV
Position: Officer / Executive
Qualification: B.Sc, M.Sc, B.Pharm
Experience: 2–7 Years
Key Responsibilities:
- Analysis of FP, IP and Stability samples
- Handling HPLC, GC, UV, FTIR and Dissolution instruments
- Analytical Method Validation and Method Verification
- Technology Transfer activities for raw materials and formulations
Quality Assurance – Lab QA, IPQA & QMS
Position: Officer / Executive
Qualification: B.Pharm, M.Pharm
Experience: 2–6 Years
Lab QA Responsibilities
- Review validation and qualification protocols
- Stability and product release documentation review
- Audit trail review and data integrity compliance
IPQA Responsibilities
- Line clearance and in-process checks
- Calibration verification activities
- Sampling and validation batch monitoring
QMS Responsibilities
- Change Control, Deviation and CAPA handling
- Documentation management and training coordination
- QMS compliance activities
ITQA (Information Technology Quality Assurance)
Position: Officer / Sr. Officer / Executive
Qualification: BCA, BE (IT), Diploma in IT
Experience: 5–8 Years
Key Responsibilities:
- Computerized System Validation (CSV)
- PLC/SCADA controlled equipment validation
- GMP and GxP compliance activities
- Qualification and validation documentation
- Compliance with 21 CFR Part 11 and EU Annex 11
Production – Manufacturing
Position: Executive / Sr. Executive
Qualification: B.Pharm, M.Pharm
Experience: 6–8 Years
Key Responsibilities:
- Supervise manufacturing operations
- Review SOPs, BOM, BMR and BPR documents
- Handle Change Control, Deviation and CAPA activities
- Improve manufacturing processes and equipment utilization
Production – Packing
Position: Packing Officer / Sr. Officer
Qualification: Any Graduate, Undergraduate, Diploma, ITI
Experience: 3–6 Years
Key Responsibilities:
- Operate bottle packing and packaging equipment
- Perform calibration and verification activities
- Maintain production records and documentation
- Ensure compliance with GMP requirements
Engineering & Projects
Department: Electrical / Mechanical
Position: Trainee Engineer
Qualification: Engineering Diploma or Degree (Mechanical/Electrical)
Experience: 0–1 Year
Key Responsibilities:
- Support engineering and project activities
- Assist preventive maintenance programs
- Maintain GMP documentation
Formulation Development Scientist (OSD)
Qualification: M.Pharm / B.Pharm
Experience: 2–6 Years
Job Responsibilities:
- Formulation development of OSD products
- Pre-formulation studies and literature review
- ANDA and EU project support
- Lab-scale batch execution and optimization
Technology Transfer Scientist
Qualification: M.Pharm / B.Pharm
Experience: 3–6 Years
Job Responsibilities:
- Coordinate technology transfer projects
- Support scale-up and manufacturing transfer activities
- Maintain project timelines and documentation
- Ensure successful transfer from development to manufacturing
Analytical Research & Development (ARD)
Qualification: M.Pharm / B.Pharm / M.Sc
Experience: 3–6 Years
Job Responsibilities:
- Stability studies and analytical support
- Analytical method development and validation
- Method transfer activities
- Investigation of analytical issues
Drug Regulatory Affairs (DRA)
Qualification: M.Pharm
Experience: 2–5 Years
Job Responsibilities:
- Regulatory documentation and submissions
- DMF, BMR, BPR and specification review
- ANDA submission support
- eCTD documentation preparation
- Knowledge of USFDA and EU regulations
Walk-In Interview Details
Date: 28 June 2026 (Sunday)
Time: 9:00 AM to 5:00 PM
Venue:
Hotel Nakshatra
Plot No. K-1, Additional MIDC,
Near Anand Nagar, Ambernath (East),
Maharashtra
Documents Required
Candidates should carry:
- Updated Resume
- Passport Size Photograph
- Latest Increment Letter
- Last 3 Months Salary Slips
- CTC Breakup Details
Apply by Email
Candidates unable to attend the walk-in interview may send their updated resume mentioning Total Experience, Current CTC, Expected CTC, Notice Period and Department to:
