V-Ensure Pharma – Walk-In Interviews for Quality Control / Quality Assurance / Production / Packing / Engineering Departments on 28th June 2026
June 26, 2026
V-Ensure Pharma Technologies Pvt. Ltd. is a reputed pharmaceutical company engaged in the development, manufacturing, and marketing of oral solid dosage (OSD) formulations for regulated markets. With USFDA and EU-GMP approved manufacturing facilities, the company is committed to quality, innovation, and regulatory compliance. V-Ensure Pharma Technologies is conducting a walk-in drive for multiple openings across Quality Control, Quality Assurance, Production, Packing, and Engineering departments at its Panvel facility.
Job Highlights
| Details | Information |
|---|---|
| Company | V-Ensure Pharma Technologies Pvt. Ltd. |
| Industry | Pharmaceutical – OSD Formulations |
| Job Type | Walk-in Interview |
| Manufacturing Facility | N-32, Additional Patalganga MIDC, Panvel, Raigad |
| Walk-in Date | 28th June 2026 (Sunday) |
| Interview Time | 9:00 AM – 5:00 PM |
| Interview Venue | Hotel Nakshatra, Plot No. K-1, Additional MIDC, Near Anand Nagar, Ambernath (East), Maharashtra |
Current Openings
| Department | Section | Position | Qualification | Experience |
|---|---|---|---|---|
| Quality Control / Analytical Lab | Stability Studies, FP/IP, GLP, AMV, TT | Officer / Executive | B.Sc., M.Sc., B.Pharm | 2–7 Years |
| Quality Assurance | Lab QA (QC-QA), IPQA & QMS | Officer / Executive | B.Pharm / M.Pharm | 2–6 Years |
| Quality Assurance | ITQA | Officer / Sr. Officer / Executive | BCA, B.E. (IT), Diploma (IT) | 5–8 Years |
| Production | Manufacturing | Executive / Sr. Executive | B.Pharm / M.Pharm | 6–8 Years |
| Production | Packing | Packing Officer / Sr. Officer | Any Graduate / Undergraduate / Diploma / ITI | 3–6 Years |
| Engineering & Projects | Electrical / Mechanical | Trainee Engineer | Engineering Diploma / Degree (Mechanical/Electrical) | 0–1 Year |
Key Responsibilities
Quality Control – Analytical Lab
- Perform analysis of finished products, stability samples, and raw materials.
- Operate analytical instruments such as HPLC, GC, UV, FTIR, and Dissolution.
- Conduct method validation, verification, and technology transfer.
- Review stability protocols, calibration, qualification documents, and analytical reports.
Quality Assurance
- Handle Lab QA, IPQA, and QMS activities.
- Perform line clearance, in-process checks, calibration verification, and IPQA sampling.
- Manage deviations, CAPA, change controls, documentation, and SOP compliance.
- Review batch manufacturing records and quality documents.
ITQA
- Validate computerized systems, software, PLC, SCADA, and CSV documentation.
- Conduct risk assessments and ensure GxP compliance.
- Prepare validation plans, reports, SOPs, and qualification documentation.
Production – Manufacturing
- Supervise manufacturing operations and production personnel.
- Ensure compliance with SOPs, BMRs, BPRs, and validation protocols.
- Handle QMS documentation including deviations, CAPA, incidents, and change controls.
- Drive continuous process improvements.
Production – Packing
- Operate and maintain bottle packing equipment, labelers, cotton inserters, sachet desiccant inserters, and related machinery.
- Perform weighing balance calibration and verification.
- Maintain production documentation and packing records.
Engineering & Projects
- Support engineering projects and preventive maintenance activities.
- Assist in equipment installation, qualification, and maintenance.
- Ensure documentation complies with GMP requirements.
Documents to Carry
- Updated Resume
- Passport-size Photograph
- Latest Increment Letter
- Last 3 Months’ Salary Slips
Unable to Attend the Walk-in?
Candidates who are unable to attend the interview can send their updated resume mentioning Total Experience, Current CTC, Expected CTC, Notice Period, and Department to:
Why Join V-Ensure Pharma Technologies?
- Work with a USFDA & EU-GMP approved pharmaceutical manufacturing organization.
- Opportunities across Quality, Production, Engineering, and IT Quality functions.
- Exposure to regulated market manufacturing and global quality standards.
- Excellent learning and career growth opportunities in the pharmaceutical industry.
