Innoxel Walk-in QC, QA, Micro, Engineering.

B.Pharm, MSc 50+ Vacancies at Innoxel Vadodara

B.Pharm, M.Pharm, BSc, MSc hiring for 50+ vacancies in Vadodara. Walk-in on 22 Feb 2026 for QC, QA, Micro, Engineering.

Innoxel Lifesciences Pvt. Ltd. is conducting a large-scale walk-in drive for multiple pharmaceutical manufacturing and quality roles. If you have experience in sterile USFDA-regulated facilities and want stable growth in injectable manufacturing, quality assurance, validation, engineering, or warehouse operations, this is a serious opportunity. The company is hiring across departments including Quality Control, Sterile Manufacturing, QC Microbiology, Quality Assurance, Warehouse, Validation, Engineering, Project Management, and Purchase.

This hiring drive is ideal for professionals with 1 to 10 years of experience in sterile injectable plants, particularly those with exposure to USFDA-compliant pharmaceutical manufacturing systems.

Company Overview

Innoxel Lifesciences Pvt. Ltd. operates in the sterile and liquid oral pharmaceutical manufacturing segment. The company focuses on regulated market production, including facilities aligned with USFDA guidelines and global GMP compliance standards.

Sterile injectable manufacturing is one of the most technically demanding segments in the pharmaceutical industry. It requires strict environmental monitoring, contamination control strategy, validated systems, and robust quality management systems. Innoxel’s operations span across sterile production lines, validation systems, HVAC utilities, warehouse compliance, and quality laboratories.

For professionals aiming to build careers in high-paying pharma jobs such as pharmaceutical quality control analyst, QA executive, validation officer, sterile production supervisor, or engineering technician in regulated plants, this walk-in drive provides direct exposure to compliance-driven manufacturing environments.

Job Role & Responsibilities

Innoxel Lifesciences is hiring for the following departments and roles:

Quality Control (QC)

Roles: Chemist & Analysts (Analytical Method Validation, RM/PM Testing)

Experience: 1–10 Years

Key Responsibilities:

• Analytical method validation and verification
• Raw Material (RM) and Packing Material (PM) testing
• Handling HPLC, GC, UV-Visible instruments
• Stability sample analysis
• Documentation as per USFDA and GMP requirements
• Investigation handling and OOS/OOT documentation

This role is suitable for candidates targeting pharmaceutical analytical chemistry jobs and regulated QC laboratory careers.

Sterile / Liquid Oral Manufacturing

Roles: Operators & Supervisors (SKID Operation, Autoclave, Vial Washing, Tunnel, Filling, Manufacturing)

Experience: 1–8 Years

Key Responsibilities:

• Operating sterile injectable equipment
• Managing autoclave sterilization cycles
• Vial washing and depyrogenation tunnel handling
• Filling line operation and supervision
• Batch manufacturing documentation
• Ensuring compliance with aseptic processing standards

Candidates with hands-on experience in sterile injectable manufacturing and USFDA-approved plants will have preference.

QC Microbiology

Roles: Microbiologists (EM & Analysts)

Experience: 1–8 Years

Key Responsibilities:

• Environmental Monitoring (EM)
• Sterility testing and microbial limit testing
• Water system monitoring
• Media preparation and culture handling
• Documentation aligned with GMP and regulatory audit standards

Microbiology professionals with sterile injectable experience are highly valued in pharmaceutical compliance-driven organizations.

Quality Assurance (QA)

Roles: Sr. Officer / Executive (QMS, Validation, VQ, IPQA, Compliance)

Experience: 4–10 Years

Key Responsibilities:

• Managing Quality Management Systems (QMS)
• IPQA oversight in sterile production areas
• Process validation and qualification (VQ)
• Handling deviations, CAPA, change control
• Audit preparation (USFDA and regulatory inspections)

This role directly contributes to regulatory compliance and pharmaceutical quality assurance leadership.

Warehouse

Roles: Warehouse Operators / Officers

Experience: 1–8 Years

Key Responsibilities:

• Inventory control and stock management
• Material inward and outward documentation
• Compliance with GMP storage practices
• Coordination with production and QC teams

Validation

Roles: Sr. Officer / Executive

Experience: 3–7 Years

Key Responsibilities:

• Equipment qualification (IQ/OQ/PQ)
• Process validation in sterile manufacturing
• Cleaning validation documentation
• Risk assessment and compliance documentation

Engineering

Roles: Technicians / Officers / Executive (PM, HVAC, Utility)

Experience: 1–8 Years

Key Responsibilities:

• Preventive maintenance (PM)
• HVAC system management in sterile areas
• Utility system monitoring
• Equipment troubleshooting in GMP environments

Project Management

Experience: 2–4 Years

• Handling pharmaceutical plant expansion projects
• Coordinating cross-functional teams
• Timeline and compliance monitoring

Purchase Department

Roles: Officers

Experience: 1–5 Years

• Vendor coordination
• Procurement documentation
• Compliance with regulated sourcing standards

Eligibility / Qualifications

Educational Qualification (Department-wise)

Quality Control: B.Sc., M.Sc., B.Pharm, M.Pharm (Chemistry background, sterile USFDA experience)

Manufacturing Operators: ITI, Diploma (Sterile USFDA experience)

Manufacturing Officers: B.Pharm, M.Pharm (Sterile USFDA experience)

Microbiology: B.Sc., M.Sc. Microbiology (Sterile USFDA experience)

Quality Assurance & Validation: B.Pharm, M.Pharm (Sterile USFDA experience)

Warehouse: ITI, B.Sc., B.Com (Sterile USFDA experience)

Engineering Technicians: ITI

Supervisory Staff (Engineering): Diploma, B.E.

Project Management: M.Pharm with injectable experience

Purchase: Any graduate with sterile USFDA experience

Relevant courses include: Pharmaceutical Sciences, Pharmaceutics, Pharmaceutical Technology, Analytical Chemistry, Organic Chemistry, Microbiology, Biotechnology, Industrial Pharmacy, Life Sciences, Mechanical Engineering, Electrical Engineering.

Location & Walk-In Details

Company: Innoxel Lifesciences Pvt. Ltd.

Walk-In Date: 22 February 2026 (Sunday)

Time: 10:00 AM to 4:00 PM

Walk-In Address:
Survey No. 534/1, Village: Kotambi
Near VCA Stadium
Taluka: Waghodia
Vadodara, Gujarat

Vadodara is a major pharmaceutical manufacturing hub in Gujarat with strong regulatory plant presence and long-term career growth potential.

Application Process

Candidates who are unable to attend the walk-in interview can share their updated resume at:

hr1@innoxells.com

Ensure your resume clearly mentions:

• Department applied for
• Years of sterile USFDA experience
• Technical skills (HPLC, EM, Validation, HVAC, Filling Line, QMS etc.)
• Current CTC and notice period

Shortlisted candidates will be contacted by the HR department for further evaluation.

Why Join Innoxel Lifesciences?

• Exposure to USFDA-regulated sterile manufacturing
• Multi-department hiring with long-term stability
• Strong compliance and validation systems
• Opportunity to work in injectable manufacturing environment
• Career growth in pharmaceutical quality assurance and validation domains

Professionals seeking pharmaceutical manufacturing jobs in Vadodara, QC analyst careers in sterile plants, QA executive roles in regulated facilities, or validation officer positions in USFDA-approved companies should seriously consider this opportunity.

Frequently Asked Questions (FAQs)

1. Is sterile USFDA experience mandatory?

Yes, preference will be given to candidates with experience in USFDA-approved sterile facilities.

2. Can freshers apply?

This drive primarily targets experienced professionals (1–10 years).

3. Are multiple departments hiring?

Yes. QC, QA, Manufacturing, Microbiology, Warehouse, Validation, Engineering, Project Management, and Purchase departments are hiring.

4. Is there an option to apply by email?

Yes. Candidates can send their resume to hr1@innoxells.com.

5. What salary range can be expected?

Salary will depend on experience, department, and technical expertise in sterile pharmaceutical manufacturing.

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Job Summary Table

Company	Innoxel Lifesciences Pvt. Ltd.
Vacancies	QC Chemist & Analyst, Manufacturing Operator & Supervisor, Microbiologist, QA Sr. Officer/Executive, Warehouse Officer, Validation Executive, Engineering Technician/Officer, Project Management, Purchase Officer
Required Education	B.Sc., M.Sc., B.Pharm, M.Pharm, ITI, Diploma, B.E., B.Com, Any Graduate (with Sterile USFDA Experience)
Experience	1–10 Years (Department-wise as specified)