Innoxel Lifesciences Pvt. Ltd., a leading emerging CDMO specializing in aseptic manufacturing of injectable vials, pre-filled syringes, and oral liquids, is actively expanding its team. With a state-of-the-art facility compliant with USFDA and EU GMP standards, the company is inviting qualified candidates for walk-in interviews on Sunday, 22nd February 2026, from 10:00 AM to 4:00 PM.
This is an excellent opportunity for professionals with experience in sterile operations and regulated markets to join a dynamic organization focused on quality and innovation in the pharmaceutical sector.
Available Positions and Departments
Innoxel Lifesciences is recruiting across several key departments for experienced candidates, particularly those with sterile USFDA exposure:
- Quality Control Roles: Chemist & Analysts (Analytical Method Validation, RM/PM) Experience: 1-10 years Education: B.Sc./M.Sc. (Chemistry), B.Pharm/M.Pharm
- Sterile/Liquid Oral Manufacturing Roles: Operators & Supervisors (SKID Operation, Autoclave, Washing/Tunnel/Manufacturing/Vial Filling) Experience: 1-8 years Education: ITI/Diploma for Operators; B.Pharm/M.Pharm for Officers (Sterile USFDA Exp.)
- QC Microbiology Roles: Microbiologists (EM & Analysts) Experience: 1-8 years Education: B.Sc./M.Sc. Microbiology (Sterile USFDA Exp.)
- Quality Assurance Roles: Sr. Officers/Executives (Qualification & Validation, QMS, VQ/IPQA/Compliance) Experience: 4-10 years Education: B.Pharm/M.Pharm (Sterile USFDA Exp.)
- Warehouse Roles: Warehouse Operators/Officer Experience: 1-8 years Education: ITI/B.Sc./B.Com (Sterile USFDA Exp.)
- Validation Roles: Sr. Officer/Officers/Executive Experience: 3-7 years Education: B.Pharm/B.Sc. Pharm (Sterile USFDA Exp.)
- Engineering Roles: Technicians/Officers/Executive (PM/HVAC/Utility) Experience: 1-8 years Education: ITI (for Technicians); Diploma/B.E. (for Supervisory Staff)
- Project Management Roles: Project Management Officers Experience: 2-4 years Education: Relevant qualification
- Purchase Roles: Officers Experience: 1-5 years Education: M.Pharm (with relevant experience in Injectables)
Key Responsibilities (General Across Roles)
- Perform day-to-day operations in respective departments while adhering to cGMP, USFDA, and other regulatory guidelines.
- Ensure product quality, documentation, validation, and compliance in sterile manufacturing environments.
- Handle equipment operations, testing, analysis, and troubleshooting.
- Maintain records, participate in audits, and support continuous improvement initiatives.
Candidates with hands-on experience in sterile USFDA-approved facilities will be preferred.
Required Qualifications and Skills
- Relevant educational background as specified for each role.
- Prior experience in pharmaceutical manufacturing, especially sterile injectables and USFDA-regulated environments.
- Strong knowledge of GMP, validation, microbiology, analytical techniques, or engineering utilities.
- Ability to work in shifts and a fast-paced production setting.
Salary and Benefits
While specific salary details vary by role, experience, and negotiation, Innoxel Lifesciences offers competitive compensation in the pharmaceutical industry. Typical ranges for these positions in Vadodara/Gujarat include:
- Entry to mid-level (1-5 years): ₹2.5 – 6 LPA
- Senior roles (5-10+ years): ₹6 – 12 LPA or higher Benefits often include health insurance, performance incentives, professional development, and a supportive work environment in a modern facility.
How to Apply
Attend the walk-in interviews on 22nd February 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, India – 391510
Bring your updated resume, educational certificates, experience letters, and salary proofs.
Candidates unable to attend the walk-in can email their resumes to hr1@innoxells.com (mention “Sterile USFDA Exp.” in the subject if applicable).
Don’t miss this chance to build your career with a forward-thinking CDMO in the pharma sector!
