V-Ensure Pharma Technologies Walk-in Production & QA

• Company Overview
• Job Roles & Responsibilities
• Quality Assurance (QA) Department
• Production Department
• Eligibility / Qualifications
• Location & Salary
• Application Process
• Why Join V-Ensure Pharma?
• FAQs
• Summary Table

B Pharm/M.Pharm Production & QA Jobs at V-Ensure, Raigad

Walk-in for Production & QA roles at V-Ensure Pharma, USFDA & EU-GMP approved OSD facility. B Pharm/M.Pharm graduates, 2–6 yrs experience.

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V-Ensure Pharma Technologies Pvt. Ltd, a leading pharmaceutical company specializing in oral solid dosage (OSD) formulations, is conducting a walk-in drive for multiple positions at its USFDA & EU-GMP approved manufacturing facility located at N-32, Additional Patalganga MIDC, Tal. Panvel, Dist. Raigad. This is an exceptional opportunity for professionals seeking growth in production and quality assurance roles in a regulated and internationally compliant environment.

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Company Overview

V-Ensure Pharma Technologies Pvt. Ltd is a reputable pharmaceutical organization engaged in the development, manufacturing, and marketing of oral solid dosage forms for regulated markets. With a strong emphasis on compliance with USFDA and EU-GMP standards, the company is committed to delivering high-quality products, implementing rigorous quality control measures, and providing a collaborative environment for career development.

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Job Roles & Responsibilities

Quality Assurance (QA) Department

Section: QMS & QA

Positions: Officer, Sr. Officer, Executive

Experience: 2–6 Years

Qualification: B Pharm, M.Pharm, MSc

Key Responsibilities:

• Manage QMS activities including Change Control, Deviation, CAPA, and Training Management.
• Coordinate new product initiation, evaluation, and tracking.
• Review sectional and cross-functional SOPs to ensure CGMP, GDP, and data integrity compliance.
• Review method validation/verification protocols, stability protocols, and calibration/qualification documents.
• Evaluate raw material and packaging material specifications (MOL).
• Analyze stability and finished product data, COA, and summary reports.
• Hands-on experience in QC testing of release and stability samples and reviewing electronic audit trails.

Production Department

Sections: BOS, Granulation, Primary & Secondary Packing

Positions: Operator, Sr. Operator

Experience: 2–4 Years

Qualification: Any Graduate/Undergraduate/Diploma, B Pharm, D.Pharm, BSc

Key Responsibilities:

• Handle daily manufacturing and packing operations using equipment such as Mister Packing Machine-BQ5, Antras, Pam Pack, HSMG-250, FBP, Wruster Coater, Blender, Multimill, Comill.
• Perform weighing balance calibration and verification.
• Maintain detailed production area documentation and logbooks.
• Execute cleaning and maintenance activities for all production equipment and instruments according to SOPs.
• Ensure compliance with CGMP standards in production and packing areas.

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Eligibility / Qualifications

• Educational Requirements: B Pharm, M.Pharm, MSc, D.Pharm, BSc, or any relevant undergraduate/graduate degree.
• Experience: 2–6 years for QA, 2–4 years for Production.
• Skills & Attributes:
  • Strong understanding of CGMP, GDP, SOPs, and QMS.
  • Hands-on experience in QC testing, stability evaluation, and production equipment operation.
  • Excellent documentation and record-keeping skills.
  • Ability to multitask, coordinate with cross-functional teams, and adhere to regulatory standards.
• Preferred: Male candidates for QA Officer roles.

Relevant Courses: B Pharm, M.Pharm, MSc, D.Pharm, BSc, Diploma in Pharmaceutical Sciences, Production/QA related certifications.

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Location & Salary

• Location: N-32, Additional Patalganga MIDC, Tal. Panvel, Dist. Raigad, Maharashtra. Landmark: Near Balaji Formalin.
• Salary: Competitive, commensurate with experience and qualification.
• Opportunity for career growth in USFDA & EU-GMP compliant OSD manufacturing environment.

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Application Process

Walk-in Interview Details:

• Date & Time: 27th September 2025, Saturday, 02:00 PM – 05:00 PM
• Venue: N-32, Additional Patalganga MIDC, Tal. Panvel, Dist. Raigad, Maharashtra.
• Documents Required: Updated CV, passport-size photograph, and educational certificates.

Note: Candidates must attend the walk-in with all required documents. Incomplete applications may not be considered.

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Why Join V-Ensure Pharma?

• Work in a USFDA & EU-GMP approved OSD facility, gaining exposure to regulated manufacturing standards.
• Hands-on experience with advanced production and analytical equipment.
• Opportunity to develop expertise in QMS, QA, and CGMP-compliant production processes.
• Collaborative work environment with opportunities for training, upskilling, and professional growth.
• Contribute to high-quality pharmaceutical product development impacting global healthcare.

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FAQs

1. Who is eligible for these positions?
Candidates with B Pharm, M.Pharm, MSc, D.Pharm, BSc, Diploma, or equivalent degrees with relevant experience in production or QA.

2. What is the experience requirement?
QA: 2–6 years | Production: 2–4 years.

3. Are freshers eligible?
Not specified; preference for experienced candidates.

4. What documents are needed for the walk-in?
Updated CV, passport-size photo, and educational certificates.

5. Where is the interview location?
N-32, Additional Patalganga MIDC, Tal. Panvel, Dist. Raigad, Maharashtra.

6. How to prepare for QA & Production roles?
Familiarity with CGMP, SOPs, QC testing, production equipment, and documentation practices.

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Summary Table

Category	Details
Company	V-Ensure Pharma Technologies Pvt. Ltd
Vacancies	QA Officer/Sr. Officer/Executive, Production Operator/Sr. Operator
Required Education	B Pharm, M.Pharm, MSc, D.Pharm, BSc, Diploma
Experience	2–6 years for QA, 2–4 years for Production
Location	N-32, Additional Patalganga MIDC, Tal. Panvel, Dist. Raigad
Contact	Walk-in on 27th Sep 2025, 02:00–05:00 PM