Innoxel Lifesciences Walk-in Interview for Pharma Jobs in QC, Production & More on 28th September

Discover top pharma jobs in India with Innoxel Lifesciences’ walk-in interview on September 28, 2025. Explore QC jobs, sterile manufacturing roles, and QA opportunities in Vadodara.

About the Company

Innoxel Lifesciences Pvt. Ltd. stands as a dynamic Contract Development and Manufacturing Organization (CDMO) in Vadodara, India. Specializing in aseptic and terminal sterilized production of injectable vials, pre-filled syringes, and oral liquids, the company excels in niche therapies like oncology and critical care.

With a state-of-the-art 350,000 sq.ft facility featuring advanced barrier technology and 21CFR Part 11 compliance, Innoxel boasts a successful USFDA inspection in 2025. Employing over 120 top professionals, it drives innovation and growth in pharmaceutical careers. Its commitment to global quality benchmarks ensures reliable supply to regulated markets like the US and EU.

Job Details

• Company Name: Innoxel Lifesciences Pvt. Ltd.
• Experience: 1-10 years
• Qualification: ITI, Diploma, B.Sc., M.Sc., B.Pharm, M.Pharm, B.Com (with focus on Chemistry, Microbiology)
• Location: Survey No. 534/1, Village: Kotambi, Nr. VCA Stadium, Tal.: Waghodia, Vadodara, Gujarat
• Work Type: On-site, Full-time in sterile manufacturing environment

Job Description

Innoxel Lifesciences is actively hiring for multiple positions in quality control, sterile manufacturing, microbiology, and warehousing to support its expanding CDMO operations.

These pharma jobs in India emphasize sterile USFDA-compliant expertise, offering dynamic roles in a cutting-edge facility. Ideal for professionals seeking pharmaceutical careers in Vadodara, the openings span analytical validation to operational supervision.

Quality Control

• Department: Quality Control
• Role: Analytical Method Validation RM/PM, SPEC/STP/Protocol & Report Preparation
• Experience: 1-10 years
• Education/Qualification: B.Sc./M.Sc./B.Pharm/M.Pharm in Chemistry (Sterile USFDA Experience required)

Sterile Manufacturing

• Department: Sterile Manufacturing
• Role: Operators & Supervisors for Filling, Autoclave, Vial Washing/Tunnel
• Experience: 1-8 years
• Education/Qualification: ITI/Diploma for Operators; B.Pharm/M.Pharm for Officers (Sterile USFDA Experience required)

QC Micro

• Department: QC Micro
• Role: Environment Monitoring & Microbiologist
• Experience: 1-8 years
• Education/Qualification: B.Sc./M.Sc. in Microbiology (Sterile USFDA Experience required)

Warehouse

• Department: Warehouse
• Role: Officer for Warehousing Management, Dispensing & Store
• Experience: 1-7 years
• Education/Qualification: B.Sc./M.Sc./B.Com (Sterile USFDA Experience required)

Skills/Qualifications

• Strong background in sterile USFDA-compliant processes for injectables and aseptic production
• Proficiency in analytical method validation, protocol development, and report writing (for QC roles)
• Hands-on experience with filling, autoclave operations, vial washing, and tunnel loading (for manufacturing)
• Expertise in environmental monitoring, microbiological testing, and lab techniques (for QC Micro)
• Knowledge of warehousing management, dispensing, inventory control, and GMP standards
• Relevant degrees: B.Sc./M.Sc. in Chemistry/Microbiology, B.Pharm/M.Pharm, ITI/Diploma, or B.Com
• 1-10 years of experience in pharmaceutical manufacturing or quality assurance

Key Responsibilities

• Conduct analytical method validation for raw materials and packaging materials in QC
• Prepare specifications, standard test procedures, protocols, and compliance reports
• Operate and supervise sterile processes including filling, autoclaving, and vial preparation
• Perform environmental monitoring and microbiological analysis to ensure product sterility
• Manage warehouse operations, including dispensing materials and maintaining accurate stores
• Adhere to USFDA guidelines, GMP practices, and safety protocols in all activities
• Collaborate with cross-functional teams to support production and quality goals

Benefits/Perks

• Competitive salary packages aligned with industry standards for pharma jobs in India
• Opportunities for career growth in a rapidly expanding CDMO with global reach
• Continuous learning through training in USFDA compliance and advanced technologies
• Supportive work culture fostering innovation and professional development
• Health insurance, on-site facilities, and employee wellness programs
• Stable long-term roles in a compliant, high-tech sterile manufacturing environment

How to Apply

If unable to attend the walk-in, email your updated resume to hr1@innoxells.com with the subject “Application for [Role Name] – Vadodara“.

Verified Post

The post is released by the Innoxel Lifescience LinkedIn page. Click here to visit the post

For more pharma job resources, bookmark Pharma Recruiter. Join Innoxel Lifesciences today—apply now!

Walk-in Interview Details

• Date: September 28, 2025 (Sunday)
• Time: 10:00 AM to 4:00 PM
• Venue: Innoxel Lifesciences Pvt. Ltd., Survey No. 534/1, Village: Kotambi, Nr. VCA Stadium, Tal.: Waghodia, Vadodara, Gujarat
• Contact/Email: hr1@innoxells.com for queries or resume submission

Why You Should Join?

Innoxel Lifesciences offers unparalleled opportunities in pharmaceutical careers, blending cutting-edge sterile manufacturing with USFDA-compliant excellence. Thrive in a collaborative culture that values innovation, where your expertise in QC jobs or production roles drives real impact in oncology and critical care therapies.

With recent USFDA approval and ambitious growth plans, enjoy long-term stability, skill enhancement, and a chance to contribute to global health solutions. Elevate your pharma journey in Vadodara’s vibrant ecosystem.

FAQs