V-Ensure Pharma Technologies Pvt. Ltd., a distinguished pharmaceutical company specializing in the development, manufacturing, and marketing of Oral Solid Dosage (OSD) forms for regulated markets, invites competent and growth-oriented professionals to join our USFDA and EU-GMP approved facility at N-32, Additional Patalganga MIDC, Tal. Panvel, Dist. Raigad, Maharashtra. We are hosting a Walk-In Drive to recruit talent for our Quality Control, Quality Assurance, Project & Engineering, HR & Admin, and Warehouse departments.
Interview Details
- Date: Sunday, May 4, 2025
- Time: 9:00 AM to 5:00 PM
- Venue: Hotel Woodland, N.H. No. 48, Near Tejpal Motors, Balitha, Vapi-396191, Gujarat
Documents Required:
- Detailed resume
- Passport-size photograph
- Last increment letter
- One month’s salary slips
- Educational certificates
- Copies of Aadhar and PAN card
Contact:
- Email: n32admin@v-ensure.com and a.salunkhe@v-ensure.com
- Note: Candidates unable to attend the walk-in can email their updated resume to the above addresses with the subject line indicating the department and position (e.g., “Application for QC Officer”).
- Source Confirmation: The job posting aligns with V-Ensure’s official communications and industry job boards.
Why Join V-Ensure Pharma Technologies?
V-Ensure operates a cutting-edge OSD facility in the Patalganga MIDC, a prominent pharmaceutical hub near Panvel, Navi Mumbai. By joining us, you will:
- Work in a USFDA and EU-GMP approved facility focused on tablets and capsules for global markets
- Collaborate with a team adhering to stringent cGMP/GLP standards
- Benefit from a 3.7/5 employee rating for skill development and job security (based on 63 reviews on AmbitionBox)
- Enjoy excellent connectivity (65 km from Mumbai Airport, 3 km from Rasayani railway station)
- Contribute to a company with a commitment to quality and regulatory compliance
Note: Some reviews mention challenges with work-life balance due to shift work; candidates should discuss shift structures during the interview.
Available Positions
All positions prioritize candidates with exposure to cGMP/GLP documentation and experience in regulated plants (USFDA, EU-GMP). Immediate joiners are preferred.
1. Quality Control (QC) – Analytical Lab
- Positions: Officer / Senior Officer / Executive
- Qualification: M.Sc. / M.Pharm
- Experience: 2–7 years (data integrity experience preferred)
Job Profiles:
- Raw Material, Stability Studies, Finished Product/In-Process (FP/IP):
- Perform analysis for method validation, verification, and technology transfer
- Operate sophisticated instruments (HPLC, GC, UV, FTIR, Dissolution Apparatus)
- Conduct stability testing and review COA/summary reports
- Test raw materials, stability samples, and finished products (tablets/capsules)
- Analytical Method Technology Transfer:
- Review analytical method validation protocols and reports
- Review specifications, Method of Analysis (MOA), and DMF documentation
- Ensure compliance with regulatory standards
- Key Skills:
- Proficiency in HPLC, GC, UV, FTIR, and dissolution testing
- Strong knowledge of cGMP, GLP, and data integrity
- Experience with stability protocols and method validation
- Open Positions: Multiple
2. Quality Assurance (QA) – IPQA / Finished Product / Stability / Method Validation / GLP / Document Control
- Positions: Officer / Senior Officer / Executive
- Qualification: M.Sc. / M.Pharm
- Experience: 2–7 years
Job Profile:
- Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR)
- Review process validation protocols, cleaning validation, and hold-time study reports
- Verify raw material and packaging material specifications
- Review stability data, validation sheets, COA, and summary reports
- Manage QMS documentation and ensure cGMP/GLP compliance
Key Skills:
- Expertise in IPQA, process validation, and cleaning validation
- Strong documentation skills and regulatory knowledge
- Familiarity with QMS and GLP practices
- Open Positions: Multiple
3. Project & Engineering – Electrical
- Positions: Senior Officer / Executive
- Qualification: B.E. / B.Tech (Electrical)
- Experience: 2–7 years
Job Profile:
- Perform Planned Preventive Maintenance (PPM) for electrical equipment
- Handle breakdowns of equipment like RMG, FBD, tablet coating machines, capsule filling machines, and blister lines
- Manage documentation for qualification, requalification, and maintenance
- Ensure compliance with cGMP and safety standards
Key Skills:
- Knowledge of electrical systems in pharmaceutical plants
- Experience with equipment maintenance and troubleshooting
- Familiarity with cGMP and validation protocols
- Open Positions: Multiple
4. Project & Engineering – Mechanical
- Positions: Officer / Senior Officer
- Qualification: B.E. / B.Tech (Mechanical) / Diploma (Mechanical)
- Experience: 2–7 years
Job Profile:
- Conduct PPM and periodic maintenance for HVAC, water systems, and utility equipment
- Handle breakdowns of RMG, FBD, tablet coating, capsule filling, and blister lines
- Manage validation, calibration, and ACAD documentation
- Support engineering-to-material verification processes
Key Skills:
- Expertise in HVAC, water systems, and mechanical equipment maintenance
- Knowledge of validation, calibration, and cGMP
- Proficiency in ACAD and technical documentation
- Open Positions: Multiple
5. Project & Engineering – Apprentice
- Positions: Apprentice
- Qualification: B.Sc. / Any Diploma
- Experience: Fresher
Job Profile:
- Assist in maintenance activities for HVAC, water systems, and production equipment
- Support documentation for qualification and calibration
- Learn cGMP and regulatory compliance processes
Key Skills:
- Basic understanding of mechanical/electrical systems
- Willingness to learn and adapt to pharmaceutical processes
- Open Positions: Multiple
6. HR & Admin – Recruitment
- Positions: Senior Officer / Executive
- Qualification: Any Graduate / Postgraduate
- Experience: 1–6 years
Job Profile:
- Manage end-to-end recruitment, onboarding, and induction activities
- Handle employee life cycle management (appraisals, exits)
- Maintain HR documentation and ensure compliance with labor laws
- Support other HR and admin-related activities
Key Skills:
- Strong recruitment and employee engagement skills
- Knowledge of HRIS and compliance requirements
- Excellent communication and organizational skills
- Open Positions: Multiple
7. Warehouse – Storage & Dispensing
- Positions: Apprentice
- Qualification: Any Graduate / D.Pharm
- Experience: 1–3 years
Job Profile:
- Handle material receipts and prepare Goods Receipt Notes (GRN)
- Manage dispensing of raw materials for production
- Maintain warehouse documentation and cGMP compliance
- Support inventory management and material verification
Key Skills:
- Knowledge of warehouse operations and material handling
- Familiarity with cGMP and inventory systems
- Strong documentation and attention to detail
- Open Positions: Multiple
How to Apply
- Walk-In: Attend the interview at Hotel Woodland, Vapi, on May 4, 2025, with all required documents.
- Email Application: If unable to attend, send your updated resume to n32admin@v-ensure.com and a.salunkhe@v-ensure.com with the subject line indicating the department and position.
- Note: Candidates with experience in regulated plants (USFDA, EU-GMP) and familiarity with cGMP/GLP documentation are preferred. Ensure all documents are complete for a smooth interview process.
Application Deadline
Walk-in interviews are scheduled for May 4, 2025. Email applications are accepted on a rolling basis.
Contact Us
- Email: n32admin@v-ensure.com, a.salunkhe@v-ensure.com
- Website: www.v-ensure.com
- Facility Address: V-Ensure Pharma Technologies Pvt. Ltd., N-32, Additional Patalganga MIDC, Panvel, Maharashtra 410206
Additional Information
- Location Context: Patalganga MIDC is a key pharmaceutical hub, 65 km from Mumbai Airport and 18 km from Panvel, with excellent connectivity via Rasayani (3 km) and Apta (5 km) railway stations. The area has robust infrastructure, including 54–72 MLD water supply and 220KV/100KV power substations.
- Environmental Compliance: The facility adheres to zero-discharge norms, with a private CETP expected to be operational by mid-2025. Hazardous waste is managed through Mumbai Waste Management Ltd. (MWML).
- Company Background: V-Ensure specializes in OSD forms (tablets, capsules) for regulated markets, with a focus on quality and compliance. The facility is strategically located alongside other pharma leaders like S.G. Pharma and Cipla.
- Employee Feedback: Reviews praise skill development opportunities but note potential work-life balance challenges due to shift work. Candidates should discuss shift structures and career progression during the interview.
Join V-Ensure Pharma Technologies Pvt. Ltd. and contribute to our mission of delivering high-quality oral solid dosage forms to regulated markets. We look forward to meeting you at the walk-in drive!
