Innoxel Lifesciences Pvt. Ltd. has announced a Walk-In Interview Drive for experienced pharmaceutical professionals on 26th July 2026 (Sunday). The company is hiring for multiple departments, including Quality Control, Sterile Manufacturing, Quality Assurance, QC Microbiology, Warehouse, Engineering, Project Management, MS&T, and Validation. Candidates with sterile USFDA-regulated manufacturing experience are encouraged to attend.

If you are looking for career opportunities in the injectable pharmaceutical industry, this recruitment drive offers excellent openings across technical and operational functions.

Job Highlights

Particular Details

Company

Innoxel Lifesciences Pvt. Ltd.

Job Type

Walk-In Interview

Walk-In Date

26th July 2026 (Sunday)

Interview Time

10:00 AM – 4:00 PM

Industry

Pharmaceutical – Sterile Injectables

Experience

0–14 Years (Department-wise)

Qualification

ITI, Diploma, B.Sc, M.Sc, B.Com, B.Pharm, M.Pharm, B.E.

Preferred Experience

Sterile USFDA Manufacturing Experience

Department-wise Vacancy Details

1. Quality Control (QC)

Roles:

Officer

Senior Officer

Executive

Senior Executive

Analytical Method Validation

HPLC

Experience: 2–8 Years

Qualification:

B.Sc

M.Sc

B.Pharm

M.Pharm (Chemistry)

Sterile USFDA experience preferred

2. Sterile / Liquid Oral Manufacturing

Roles:

Operators

Officers

Executives

Functional Areas:

Skid Operation

Autoclave

Vial Washing

Tunnel

Manufacturing

Filling

Experience: 1–8 Years

Qualification:

ITI/Diploma (Operators)

B.Pharm/M.Pharm (Officer & Executive)

Sterile USFDA experience preferred

3. QC Microbiology

Role:

Microbiologist (EM & Analysts)

Experience: 1–5 Years

Qualification:

B.Sc / M.Sc Microbiology

Sterile USFDA experience preferred

4. Quality Assurance (QA)

Roles:

Deputy Manager

Senior Executive

Executive

Officer

Functional Areas:

Compliance

Qualification & Validation

IPQA

Skilled Media Fill

IT QA (CSV)

QA of QC (AMV)

Regulatory Affairs

Training Coordinator

Experience: 2–14 Years

Qualification:

B.Pharm

M.Pharm

M.Sc

Sterile USFDA experience preferred

5. Warehouse

Roles:

Operator

Officer

Executive

Experience: 0–6 Years

Qualification:

ITI

B.Sc

B.Com

Sterile USFDA experience preferred

6. Engineering

Roles:

Technician

Operator

Officer

Executive

Areas:

Plant Maintenance

QMS

Utility

Water System

Civil Engineering

Experience: 1–10 Years

Qualification:

ITI (Technicians & Operators)

Diploma / B.E. (Supervisory Staff)

7. Project Management

Role:

Assistant Manager

Experience: 6–10 Years

Qualification:

M.Pharm

Relevant Injectable Manufacturing Experience

8. MS&T (Manufacturing Science & Technology)

Role:

Senior Officer / Executive

Experience: 4–8 Years

Qualification:

B.Sc

M.Sc

B.Pharm

Sterile USFDA experience preferred

9. Validation

Role:

Senior Officer / Executive

Experience: 3–7 Years

Qualification:

B.Pharm / M.Pharm

Sterile USFDA experience preferred

Walk-In Interview Details

Date: 26th July 2026 (Sunday)

Time: 10:00 AM to 4:00 PM

Venue:

Innoxel Lifesciences Pvt. Ltd.

Survey No. 534/1, Village: Kotambi, Near VCA Stadium, Tal. Waghodia, Vadodara, Gujarat

Resume Email (If Unable to Attend):

hr1@innoxells.com

Documents to Carry

Updated Resume/CV

Recent Passport Size Photographs

Educational Certificates

Experience Certificates

Latest Salary Slips

PAN Card

Aadhaar Card

Any other relevant supporting documents

Why Join Innoxel Lifesciences?

Career opportunities in a fast-growing sterile pharmaceutical company

Exposure to USFDA-regulated manufacturing environment

Multiple technical departments and career growth options

Opportunities for experienced professionals in injectables manufacturing

Professional work culture with advanced manufacturing facilities

Technical FAQs

1. What is Analytical Method Validation (AMV) in Quality Control?

Analytical Method Validation verifies that analytical methods such as HPLC are accurate, precise, specific, linear, robust, and suitable for testing pharmaceutical products according to regulatory guidelines.

2. What is the role of IPQA in sterile manufacturing?

In-Process Quality Assurance (IPQA) monitors manufacturing activities, verifies compliance with SOPs, performs line clearance, and ensures products meet GMP and regulatory standards throughout production.

3. Why is Environmental Monitoring (EM) important in sterile manufacturing?

Environmental Monitoring evaluates the cleanliness of classified manufacturing areas by monitoring viable and non-viable particles, helping prevent microbial contamination during sterile production.

4. What is Computer System Validation (CSV)?

CSV ensures that computerized systems used in pharmaceutical manufacturing consistently perform as intended and comply with regulatory requirements such as USFDA and GMP guidelines.

5. What is the importance of Qualification and Validation?

Qualification and Validation confirm that equipment, utilities, manufacturing processes, and analytical methods consistently produce products meeting predetermined quality standards through IQ, OQ, PQ, and process validation.