V-Ensure Pharma Technologies Walk-In | QA/QC/Production

V-Ensure Pharma Technologies Walk-In | QA/QC/Production

career with V-Ensure Pharma Technologies Pvt. Ltd., a reputed pharmaceutical company specializing in oral solid dosage manufacturing for regulated markets. Our USFDA & En-GMP approved facility in Vapi, Gujarat, is conducting a walk-in recruitment drive on 09 November 2025 for multiple positions across Quality Assurance, Quality Control, Production, Validation, and Warehouse departments. Join a dynamic, growth-oriented organization recognized for innovation, regulatory compliance, and employee development.


Company Overview

V-Ensure Pharma Technologies Pvt. Ltd. is a leading pharmaceutical company focused on research, development, and manufacturing of high-quality oral solid dosage forms. Our Vapi facility strictly follows USFDA and European GMP standards, ensuring compliance with global regulations. With a culture centered on professional growth and innovation, V-Ensure Pharma Technologies empowers its employees to contribute meaningfully to healthcare advancements and global patient safety.


Job Roles & Responsibilities

Quality Assurance (QA)

Positions: Officer / Sr. Officer / Executive
Sections: ALQA, Finished Products, Stability, Method Validation Lab, QA/GLP Documentation Control
Qualifications: M.Sc / B.Pharm / M.Pharm
Experience: 2–6 Years

Key Responsibilities:

  • Review method validation, verification, and stability protocols.

  • Evaluate raw material (RM) and packaging material (PM) specifications, MOAs, and finished product COA.

  • Hands-on experience in QC testing of release and stability samples.

  • Analyze electronic data, audit trails, and integrations.

  • Conduct process validation, vendor qualification, risk assessment, hatch record review, and cleaning validation.


Validation / IPQA

Positions: Officer / Sr. Officer / Executive
Qualifications: M.Sc / B.Pharm / M.Pharm
Experience: 2–7 Years

Key Responsibilities:

  • Execute in-process checks, line clearance, and batch sampling.

  • Ensure compliance with GDP and GMP standards.

  • Perform analysis of RM, PM, FP, and IP stability.

  • Operate sophisticated instruments such as HPLC, GC, UV, FTIR, Dissolution.


Quality Control Analytical Lab

Positions: Officer / Executive
Qualifications: B.Sc / M.Sc / B.Pharm
Experience: 2–7 Years

Key Responsibilities:

  • Conduct raw material, stability, and finished product testing.

  • Execute analytical method validation and technology transfer.

  • Operate instruments including HPLC, GC, UV, FTIR, Dissolution systems.


Warehouse

Positions: Officer / Sr. Officer / Executive
Qualifications: Any Graduate
Experience: 3–5 Years

Key Responsibilities:

  • Monitor temperature and RH in storage areas.

  • Manage SOP revisions, change control, CAPA, deviations, retest, and rejected materials.

  • Oversee invoice processing and QMS documentation.


Production / Manufacturing

Positions: Operator / Sr. Operator / Officer / Sr. Officer
Qualifications: D.Pharm / Diploma / B.Pharm / M.Sc / M.Pharm
Experience: 2–8 Years

Key Responsibilities:

  • Operate compression, capsule filling, blister packing, granulation, and bottle packing machines.

  • Maintain production area logbooks and documentation.

  • Execute method verification, tech transfer, and analytical testing.

  • Ensure adherence to SOPs, GMP, and QMS standards.


Walk-In Drive Details

  • Date: 09 November 2025 (Sunday)

  • Time: 9:00 AM to 5:00 PM

  • Venue: Hotel Woodland, N.H. No. 48, Near Tejpal Motors, Balitha, Vapi – 396191, Gujarat

  • Documents to Bring: Resume, Passport-size Photo, Last Increment Letter, 3 Months Salary Slips

Note: Candidates with experience in regulated pharma environments, GMP/GLP documentation, and USFDA/EN-GMP facilities will be preferred.


Key Skills & Experience Required

  • Hands-on experience in QA, QC, Production, or Validation in regulated pharma plants.

  • Proficiency in HPLC, GC, UV, FTIR, Dissolution apparatus.

  • Knowledge of GMP, GLP, GDP, and QMS compliance.

  • Ability to manage SOPs, CAPA, change control, and deviation documentation.

  • Strong attention to detail, teamwork, and analytical thinking.


Benefits & Growth Opportunities

  • Career development in a USFDA & En-GMP approved facility.

  • Exposure to regulated domestic and international markets.

  • Hands-on experience with modern pharmaceutical equipment.

  • Work in a professional, collaborative, and growth-oriented culture.


FAQs

Q1: What documents are required for the walk-in?
A: Resume, Passport-size Photo, Last Increment Letter, 3 Months Salary Slips.

Q2: Who will be preferred?
A: Candidates with experience in USFDA/EN-GMP facilities and regulated pharma plants.

Q3: Is prior experience mandatory?
A: Yes, 2–8 years depending on the role.

Q4: Are multiple vacancies available?
A: Yes, across QA, QC, Production, Validation, and Warehouse departments.


V-Ensure Pharma Technologies Walkin

Category Details
Company V-Ensure Pharma Technologies Pvt. Ltd. – USFDA & En-GMP approved
Vacancies Multiple across QA, QC, Production, Validation, Warehouse
Required Education M.Sc, B.Pharm, M.Pharm, B.Sc, D.Pharm, Diploma, Any Graduate
Experience 2–8 Years depending on role
Reputed Pharmaceutical Walk-in QA, QC, Production, and Warehouse
Reputed Pharmaceutical Walk-in QA, QC, Production, and Warehouse

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