Explore Innoxel Lifesciences Hiring for QC / QA / Microbiology / Production / Warehouse pharma jobs.
Innoxel Lifesciences Walk-In Interview 2025 – Exciting Pharma Jobs in Vadodara
If you are looking for pharma jobs in Vadodara, here’s a great opportunity! Innoxel Lifesciences Pvt. Ltd., a reputed and USFDA-approved sterile injectables manufacturer, has announced a walk-in interview on 16 November 2025 (Sunday) for multiple departments including Quality Control (QC), Quality Assurance (QA), QC Microbiology, Production, Warehouse, and Project Management. Innoxel Lifesciences Hiring for QC / QA / Microbiology / Production / Warehouse
This recruitment drive is designed for professionals seeking to grow their careers in sterile pharmaceutical manufacturing. Whether you are an experienced professional or a skilled candidate with USFDA exposure, this walk-in event offers a platform to explore stable, rewarding pharma job opportunities in Gujarat. Innoxel Lifesciences Hiring for QC / QA / Microbiology / Production / Warehouse
Innoxel Lifesciences is expanding its operations at its modern sterile injectables facility in Kotambi, Vadodara, and is looking for dedicated and qualified candidates across various levels. Innoxel Lifesciences Hiring for QC / QA / Microbiology / Production / Warehouse
About Innoxel Lifesciences Pvt. Ltd.
Innoxel Lifesciences Pvt. Ltd. is one of India’s emerging pharmaceutical companies specializing in sterile injectable manufacturing. The company is known for its commitment to innovation, compliance, and quality excellence. With a strong focus on regulatory standards such as USFDA, MHRA, and WHO-GMP, Innoxel ensures every step of manufacturing meets global standards. Innoxel Lifesciences Hiring for QC / QA / Microbiology / Production / Warehouse
The company’s mission is to deliver high-quality sterile pharmaceutical products that cater to both domestic and international markets. Their facility in Vadodara is a state-of-the-art sterile manufacturing plant that operates under stringent quality control measures and provides an excellent environment for professionals to learn, grow, and excel in their careers. Innoxel Lifesciences Hiring for QC / QA / Microbiology / Production / Warehouse
Why Attend the Innoxel Lifesciences Walk-In Interview 2025?
Here’s why attending this walk-in interview could be a career-changing decision: Innoxel Lifesciences Hiring for QC / QA / Microbiology / Production / Warehouse
- Expanding Sterile Injectable Unit: Innoxel Lifesciences is increasing its production capacity, creating multiple openings across departments.
- Exposure to Global Standards: Work in a USFDA-compliant facility and gain international regulatory exposure.
- Career Stability and Growth: The company offers long-term career prospects with structured training and development programs.
- Competitive Salary Packages: Employees enjoy attractive pay structures aligned with industry standards.
- Ideal Work Environment: The Kotambi facility offers a modern, safe, and growth-oriented workplace.
- Reputed Pharma Brand: Known for reliability and regulatory compliance, Innoxel Lifesciences is a trusted name in India’s sterile manufacturing segment.
Available Positions at Innoxel Lifesciences
Below are the available job openings with their required qualifications, experience levels, and key responsibilities. Innoxel Lifesciences Hiring for QC / QA / Microbiology / Production / Warehouse
1. Quality Control – Analytical Method Validation Specialist (1–10 Years)
Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm (Chemistry or related specialization)
Experience: 1 to 10 years (Sterile USFDA experience required)
Responsibilities:
- Perform analytical method validation in sterile environments.
- Prepare SPEC/STP/Protocols as per guidelines.
- Ensure compliance with USFDA and GMP standards.
- Handle analytical instruments and maintain lab documentation.
- Support audits and regulatory inspections with proper QC data.
2. Sterile Manufacturing – Operators & Supervisors (1–8 Years)
Qualification: ITI / Diploma for Operators; B.Pharm / M.Pharm for Officers/Supervisors
Experience: 1 to 8 years (Sterile USFDA experience preferred)
Responsibilities:
- Operate and maintain sterile manufacturing equipment.
- Supervise production lines ensuring smooth operations.
- Maintain Batch Manufacturing Records (BMR) and production documentation.
- Ensure compliance with GMP, QMS, and regulatory guidelines.
- Support validation, aseptic processing, and equipment qualification.
3. QC Microbiology – Environment Monitoring & Microbiologist (1–8 Years)
Qualification: B.Sc / M.Sc in Microbiology
Experience: 1 to 8 years (Sterile USFDA experience preferred)
Responsibilities:
- Conduct environmental monitoring and microbial testing.
- Handle sterility testing, media preparation, and validation.
- Ensure microbial limits testing and data integrity in microbiology labs.
- Support sterility assurance programs and regulatory audits.
4. Warehouse Officer (1–7 Years)
Qualification: B.Sc / M.Sc / B.Com
Experience: 1 to 7 years (Sterile USFDA experience preferred)
Responsibilities:
- Manage inventory and material dispensing.
- Ensure GMP compliance in warehouse storage and handling.
- Maintain logbooks, material traceability, and stock records.
- Coordinate with production and QA for material requirements.
- Handle SAP/ERP-based warehouse systems (if applicable).
5. Project Management (2–4 Years)
Qualification: M.Pharm
Experience: 2 to 4 years (Injectables background mandatory)
Responsibilities:
- Oversee new injectable projects from initiation to completion.
- Manage timelines, documentation, and resource allocation.
- Ensure project activities align with USFDA and GMP standards.
- Liaise with cross-functional teams including production, QA, and engineering.
6. Quality Assurance – Sr. Officer / Executive (4–10 Years)
Qualification: B.Pharm / M.Pharm
Experience: 4 to 10 years (Sterile USFDA experience mandatory)
Responsibilities:
- Handle documentation, in-process QA (IPQA), and Micro QA.
- Conduct internal audits and support regulatory inspections.
- Review and approve BMR, BPR, deviation reports, and CAPA.
- Ensure process validation, documentation accuracy, and data integrity.
7. Production Compliance & Validation (2–5 Years)
Qualification: M.Pharm
Experience: 2 to 5 years (Sterile USFDA experience required)
Responsibilities:
- Manage process validation and qualification activities.
- Ensure production processes meet cGMP and USFDA compliance.
- Prepare and execute validation protocols (IQ/OQ/PQ).
- Work closely with QA for continuous process improvement.
Eligibility Criteria
- Education: B.Sc, M.Sc, B.Pharm, or M.Pharm (as per role).
- Experience: 1–10 years in sterile injectable manufacturing with mandatory USFDA exposure.
- Skills Required:
- Sound knowledge of GMP, GLP, and regulatory compliance.
- Experience in sterile injectables or parenteral manufacturing.
- Ability to work in a regulated environment with precision.
- Strong teamwork and communication skills.
- Preferred Candidates:
- Applicants from Vadodara or Gujarat will be given preference.
- Candidates with prior experience in sterile USFDA-approved units are highly desirable.
- Innoxel Lifesciences Hiring for QC / QA / Microbiology / Production / Warehouse
Benefits of Joining Innoxel Lifesciences
- Competitive salary packages and annual performance bonuses.
- Exposure to USFDA-approved sterile injectable projects.
- Career development opportunities through training programs.
- Work-life balance with supportive management.
- Opportunity to grow with a fast-expanding lifesciences organization.
- Access to advanced sterile technology and modern infrastructure.
Walk-In Interview Details
Date: Sunday, 16 November 2025
Time: 10:00 AM to 04:00 PM
Venue:
Innoxel Lifesciences Pvt. Ltd.
Survey No. 534/1, Village Kotambi, Near VCA Stadium,
Taluka: Waghodia, District: Vadodara, Gujarat – India.
Documents to Carry
When attending the walk-in interview, candidates must bring: Innoxel Lifesciences Hiring for QC / QA / Microbiology / Production / Warehouse
- Updated Resume/CV
- Passport-size photographs
- Educational certificates (original and photocopy)
- Experience certificates or relieving letters
- Salary slips or proof of current employment
- Proof of USFDA exposure (if applicable)
- Photo ID proof (Aadhaar, PAN, etc.)
Can’t Attend the Walk-In Interview? Apply via Email
If you are unable to attend the walk-in interview, you can still apply online.
Send your updated resume to the HR department via email. Innoxel Lifesciences Hiring for QC / QA / Microbiology / Production / Warehouse
Email ID: hr1@innoxells.com
Subject Line: Mention the position applied for (e.g., Application for QC Microbiologist – Vadodara)
How to Apply for Innoxel Lifesciences Jobs 2025
Follow these steps to apply for Innoxel Lifesciences vacancies: Innoxel Lifesciences Hiring for QC / QA / Microbiology / Production / Warehouse
- Prepare Your Resume: Highlight relevant sterile manufacturing and USFDA experience.
- Gather Documents: Keep your educational, experience, and ID proofs ready.
- Attend the Walk-In: Visit the venue on 16 November 2025 between 10:00 AM and 4:00 PM.
- Email Application: If unable to attend, send your resume to hr1@innoxells.com with the role title in the subject line.
- Follow Up: Keep in touch with the HR team for interview updates or shortlisting confirmation.
Join Innoxel Lifesciences and step into a world of sterile excellence, regulatory precision, and professional growth.
Don’t miss this opportunity to advance your pharmaceutical career in one of Gujarat’s most trusted lifesciences companies. Innoxel Lifesciences Hiring for QC / QA / Microbiology / Production / Warehouse
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