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Company overview
V-Ensure Pharma jobs for Quality Assurance, Analytical Lab QC, Production, BPharm, MPharm, MSc, ITI are available through a walk-in recruitment drive announced by V-Ensure Pharma Technologies Pvt Ltd. According to the recruitment notice, the company is engaged in the development, manufacturing and marketing of oral solid dosage forms for regulated markets. The company has mentioned a USFDA and EU-GMP approved OSD manufacturing facility at N32, Additional Patalganga MIDC, Tal-Parvel, District Raigad.
The recruitment advertisement highlights quality, innovation and better health as key themes and invites growth-oriented candidates for different functions connected with pharmaceutical manufacturing and quality operations. The available positions cover documentation and compliance activities, analytical laboratory work, quality assurance, process validation and production operations.
For candidates interested in regulated pharmaceutical manufacturing, these roles can provide exposure to areas such as QMS activities, documentation, audits, validation, analytical instruments, production equipment and compliance-related processes. Candidates should carefully match their qualification and experience with the individual position before attending the interview.
Job details
Job Title
Officer / Executive QMS / Compliance / Training Documentation and Issuance
Executive / Officer RM/PM/Stability/IP FP/AMV
Executive / Officer Lab QA and Process Validation
Compression Operator
Capsule Operator
Department
Quality Assurance (QMS), Analytical Lab/QC, Quality Assurance, Production (Operator)
Salary
N/A
The recruitment advertisement does not mention a specific salary package. Candidates can discuss salary, benefits and other employment terms during the interview or selection process.
Requirements
Skills
QMS activities including Change Control, Deviation and CAPA
Training activities in software
Document preparation and issuance
Document control
Internal audit training, scheduling, compliance and closure
MRM meeting scheduling and report preparation
Tracking MOM recommendations and updating schedules
New product initiation and evaluation tracking
Regulatory compliance and client audit preparation
Training management, approval and allocation of training
Analysis of raw materials, packing materials, finished products, in-process materials and stability samples
Hands-on operation of HPLC, GC, UV and FTIR
Dissolution testing
Method validation and verification
Stability protocols and related documentation
Calibration and qualification documentation
Review of raw material and packaging material specifications
Review of COA and stability data
Quality Control testing of release and stability samples
Electronic data, audit trail and data integrity review
Preparation of SOPs and validation protocols
Process validation reports
Hold time study and cleaning validation
Annual Product Review preparation
Continuous process verification reports
Area, equipment and instrument qualification
Compression machine documentation and coordination with Engineering for breakdowns
Capsule filling machine handling
Balance calibration and verification
Production documentation
Qualification
BPharm, MPharm, MSc, Graduate, Undergraduate, Diploma, ITI
Experience
QMS / Compliance / Training Documentation and Issuance: 3 to 8 years
Analytical Lab/QC RM/PM/Stability/IP FP/AMV: 3 to 6 years
Lab QA and Process Validation: 3 to 6 years
Compression Operator: 3 to 6 years
Capsule Operator: 3 to 6 years
Vacancies
Not yet disclosed
Interview Details
- 📁 Department: Quality Assurance (QMS)
📄 Qualification: BPharm, MPharm
📄 Experience: 3 to 8 years - 📁 Department: Analytical Lab/QC
📄 Qualification: MSc, BPharm
📄 Experience: 3 to 6 years - 📁 Department: Quality Assurance
📄 Qualification: MSc, BPharm, MPharm
📄 Experience: 3 to 6 years - 📁 Department: Production (Operator)
📄 Qualification: Graduate, Undergraduate, Diploma, ITI
📄 Experience: 3 to 6 years - 📁 Department: Production (Operator)
📄 Qualification: Graduate, Undergraduate, Diploma, ITI
📄 Experience: 3 to 6 years
Type
Walk-In Interview
Date and Time
Date: 27 September 2026, Sunday
Time: Not mentioned in the recruitment advertisement
Location/Platform
Hotel Woodland
N.H. No. 48, Near Tajpal Motors
Balitha, Vapi, Gujarat 396191
Documents Required
Updated CV/Resume
Candidates should also carry relevant educational and experience documents available with them for verification.
Candidates are advised to carry original documents along with photocopies where applicable.
How to Apply
V-Ensure Pharma jobs for Quality Assurance, Analytical Lab QC, Production, BPharm, MPharm, MSc, ITI candidates can be pursued through the announced walk-in interview on 27 September 2026.
Candidates who are unable to attend the walk-in interview can send their updated resume by email to:
a.salunkhe@v-ensure.com
career@v-ensure.com
Candidates should mention the position they are applying for clearly in their email and ensure that their latest contact details, qualification and relevant experience are included in the resume.
Role-wise Job Information
The Quality Assurance QMS position is focused on QMS and compliance-related responsibilities. The role includes Change Control, Deviation, CAPA, training activities, document control, internal audit coordination, MRM activities, new product tracking, regulatory compliance and training management. Candidates applying for this position should have 3 to 8 years of relevant experience.
The Analytical Lab/QC opening is intended for candidates experienced in RM, PM, finished product, in-process and stability analysis. The position also requires familiarity with sophisticated analytical instruments such as HPLC, GC, UV and FTIR along with dissolution testing. The listed experience requirement is 3 to 6 years.
The Lab QA and Process Validation position covers method validation and verification, stability documentation, calibration and qualification records, raw material and packaging material specification review, COA and stability data review, quality control testing, electronic data and audit trail review, SOP preparation, process validation, cleaning validation, hold time studies and Annual Product Review activities. The required experience is 3 to 6 years.
The Compression Operator position involves maintaining documentation related to compression machines and coordinating with Engineering for equipment repairs and breakdowns when required. Candidates with 3 to 6 years of experience and Graduate, Undergraduate, Diploma or ITI backgrounds can apply.
The Capsule Operator position involves handling capsule filling machines, performing balance calibration and verification activities, and maintaining appropriate production documentation. The listed experience requirement is 3 to 6 years, with Graduate, Undergraduate, Diploma or ITI qualifications accepted as mentioned in the advertisement.
Why Candidates May Consider These Roles
The positions cover several important areas of pharmaceutical manufacturing and quality operations, making the recruitment relevant to candidates who already have practical industry experience. Quality professionals can find roles connected with QMS, compliance, documentation, audits and validation, while analytical candidates can work around laboratory testing and instruments.
Production candidates can explore operator-level responsibilities involving compression and capsule filling operations. These roles also emphasize documentation, equipment handling and coordination, which are important parts of regulated pharmaceutical manufacturing.
The advertisement specifically states that candidates having exposure to regulatory documentation requirements such as cGMP and GLP and experience working in regulated plants will be preferred. Candidates should therefore highlight relevant regulated-industry experience clearly in their resumes.
Candidate Preparation Tips
Read the job description carefully and apply only for positions matching your qualification and experience.
Keep an updated CV with your current designation, total experience, key responsibilities and contact details.
Candidates from QA and QC backgrounds should clearly mention experience with QMS, validation, audits, documentation, analytical instruments, data integrity or other relevant areas.
Production candidates should mention experience with compression, capsule filling, equipment documentation and related production activities where applicable.
Carry original educational and experience documents along with copies for verification.
Dress professionally and reach the venue with sufficient time before the interview.
If you are travelling to the venue, check the route to Hotel Woodland, Balitha, Vapi, in advance.
Candidates unable to attend the walk-in can send their updated resume to the email addresses mentioned in the advertisement.
Career Opportunities at V-Ensure
V-Ensure Pharma jobs for Quality Assurance, Analytical Lab QC, Production, BPharm, MPharm, MSc, ITI provide openings across both quality and manufacturing functions. The advertised responsibilities involve regulated pharmaceutical processes, documentation, laboratory analysis, validation and production operations.
For experienced pharma professionals, matching the role requirements with actual hands-on experience is important. Candidates should focus their resumes on measurable responsibilities and relevant systems, instruments, equipment and documentation handled in previous roles.
The recruitment notice also gives preference to candidates with exposure to cGMP, GLP and regulated manufacturing environments. This makes it useful for candidates who have previously worked in regulated pharmaceutical plants and are familiar with compliance-focused working practices.
FAQs
What is the experience requirement for the V-Ensure Pharma jobs?
The advertised experience ranges from 3 to 8 years. The QMS/Compliance position requires 3 to 8 years, while Analytical Lab/QC, Lab QA and Process Validation, Compression Operator and Capsule Operator positions require 3 to 6 years.
Which qualifications are accepted for these V-Ensure Pharma jobs?
The listed qualifications include BPharm, MPharm, MSc, Graduate, Undergraduate, Diploma and ITI, depending on the specific position.
Which departments are hiring in this walk-in interview?
The recruitment covers Quality Assurance (QMS), Analytical Lab/QC, Quality Assurance Lab QA and Process Validation, and Production Operator positions for Compression and Capsule operations.
Is experience in regulated pharmaceutical plants preferred?
Yes. The advertisement states that candidates with exposure to regulatory documentation requirements such as cGMP and GLP and experience working in regulated plants will be preferred.
When and where is the walk-in interview?
The walk-in interview is scheduled for 27 September 2026, Sunday, at Hotel Woodland, N.H. No. 48, Near Tajpal Motors, Balitha, Vapi, Gujarat 396191. The advertisement does not mention an interview time.
V-Ensure Pharma jobs for Quality Assurance, Analytical Lab QC, Production, BPharm, MPharm, MSc, ITI are relevant to experienced candidates looking for opportunities in pharmaceutical quality, laboratory and production functions. Interested candidates should review the position-specific requirements, prepare an updated resume and attend the walk-in interview at the mentioned Vapi venue or email their resume to the provided recruitment addresses if they cannot attend.