Innoxel Walk-in QC, QA, and Sterile Manufacturing
- Sterile Manufacturing Openings – Innoxel Lifesciences Vadodara
- Company Overview
- Job Role & Responsibilities
- 1. Quality Control (QC)
- 2. Sterile Manufacturing (Production)
- 3. Quality Assurance (QA)
- 4. QC Microbiology
- 5. Warehouse Department
- 6. Project Management
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Join Innoxel Lifesciences?
- FAQs
Sterile Manufacturing Openings – Innoxel Lifesciences Vadodara
Walk-in interviews at Innoxel Lifesciences, Vadodara for QC, QA, and Sterile Manufacturing roles. Apply with 1–10 yrs experience in USFDA-approved facility.
Innoxel Lifesciences Pvt. Ltd., a rapidly growing pharmaceutical organization with a focus on injectable and sterile manufacturing, is conducting a Walk-in Interview for multiple departments at its Vadodara (Kotambi) facility. This opportunity is open to qualified professionals with hands-on experience in USFDA-approved sterile manufacturing environments.
If you have expertise in Quality Control, Quality Assurance, Manufacturing, or Project Management, and are ready to take your pharma career to the next level, this is your chance to join one of India’s emerging leaders in sterile formulations.
Company Overview
Innoxel Lifesciences Pvt. Ltd. is a state-of-the-art, USFDA-approved sterile manufacturing company located in Vadodara, Gujarat. The company specializes in manufacturing high-quality injectable formulations, meeting the stringent standards of regulatory authorities like the USFDA, MHRA, WHO, and EU.
With modern infrastructure, advanced quality systems, and a commitment to innovation, Innoxel Lifesciences has established itself as a trusted partner for global pharmaceutical clients. The company’s culture emphasizes continuous learning, process excellence, and employee well-being, making it one of the most sought-after workplaces in the Indian pharma sector.
Job Role & Responsibilities
Innoxel Lifesciences is inviting applications across the following departments:
1. Quality Control (QC)
Experience: 2–5 Years
Education: B.Sc / M.Sc / B.Pharm / M.Pharm (Chemistry)
Responsibilities:
- Perform analytical method validation, method transfer, and routine analysis for sterile products.
- Prepare and review specifications, STP, and analytical protocols.
- Operate analytical instruments like HPLC, GC, UV, and Dissolution apparatus.
- Ensure data integrity and adherence to cGMP and GLP guidelines.
2. Sterile Manufacturing (Production)
Experience: 1–10 Years
Education: ITI / Diploma (Operators), B.Pharm / M.Pharm (Officers)
Responsibilities:
- Operate and monitor sterile manufacturing processes, including filling, sealing, and lyophilization.
- Ensure cleanroom compliance as per USFDA and EU GMP standards.
- Maintain documentation for batch manufacturing, equipment qualification, and process validation.
- Participate in media fills, sterilization cycles, and line clearance activities.
3. Quality Assurance (QA)
Experience: 4–10 Years
Education: B.Pharm / M.Pharm
Responsibilities:
- Manage QA activities across Documentation Cell, Micro QA, and IPQA.
- Conduct document review, deviation handling, CAPA implementation, and internal audits.
- Ensure compliance with USFDA, MHRA, and WHO guidelines.
- Oversee process validation, cleaning validation, and quality risk assessments.
4. QC Microbiology
Experience: 1–8 Years
Education: B.Sc / M.Sc (Microbiology)
Responsibilities:
- Perform environmental monitoring, microbial limit testing, sterility testing, and endotoxin testing.
- Validate microbiological methods and support sterilization validation programs.
- Maintain compliance with GMP and laboratory safety practices.
- Prepare microbial data summaries and participate in regulatory audits.
5. Warehouse Department
Experience: 1–7 Years
Education: B.Sc / M.Sc / B.Com
Responsibilities:
- Handle material receipt, storage, and issue as per GMP.
- Maintain material traceability and stock control.
- Support line clearance and documentation in coordination with QA and Production.
6. Project Management
Experience: 2–4 Years
Education: M.Pharm (Injectable Experience Preferred)
Responsibilities:
- Coordinate project execution and documentation for sterile product development.
- Ensure alignment with timelines for qualification, validation, and technology transfer.
- Communicate with internal stakeholders and cross-functional teams for project updates.
Eligibility / Qualifications
Educational Qualifications:
B.Sc, M.Sc (Chemistry, Microbiology), B.Pharm, M.Pharm, ITI, Diploma, B.Com
Experience Range:
1–10 years depending on the position applied for.
Preferred Background:
Candidates with USFDA-approved sterile manufacturing experience will be given preference.
Relevant Courses (comma-separated):
B.Pharm, M.Pharm Pharmaceutics, M.Sc Chemistry, B.Sc Microbiology, Diploma in Sterile Manufacturing, Certification in GMP & GLP, QA/QC Data Integrity Training.
Location & Salary
Work Location: Innoxel Lifesciences Pvt. Ltd., Kotambi, Vadodara, Gujarat
Walk-in Date: Sunday, 16th November 2025
Walk-in Time: 10:00 AM to 4:00 PM
Venue: Survey No. 534/1, Village Kotambi, Near VCA Stadium, Tal: Waghodia, Vadodara
Salary: Competitive remuneration based on experience and role
Employment Type: Full-time, On-site
Perks & Benefits:
- Exposure to global quality systems and regulatory standards.
- Opportunities for professional growth and skill enhancement.
- Supportive work environment promoting safety and compliance.
Application Process
Walk-in Interview:
Date: 16th November 2025 (Sunday)
Time: 10:00 AM – 4:00 PM
Venue: Innoxel Lifesciences Pvt. Ltd., Kotambi, Vadodara
Candidates unable to attend the walk-in can share their resumes via email.
Email: hr1@innoxells.com
Documents to Carry:
- Updated Resume (Hardcopy)
- Educational Certificates
- Latest Salary Slips / CTC Breakup
- Passport-size Photo
- ID Proof
Note: Preference will be given to candidates with experience in sterile injectables and regulatory audit exposure.
Why Join Innoxel Lifesciences?
- Work in a USFDA-approved, world-class sterile manufacturing facility.
- Collaborate with talented professionals in Quality, Production, and R&D.
- Gain hands-on exposure to international regulatory practices.
- Build a career with a company that values quality, compliance, and innovation.
FAQs
Q1. Who can apply for Innoxel’s walk-in drive?
A1. Professionals with 1–10 years of experience in sterile or injectable manufacturing, QA, QC, or microbiology can apply.
Q2. Is experience in sterile manufacturing mandatory?
A2. Yes, preference will be given to candidates with sterile or USFDA audit experience.
Q3. Can freshers apply?
A3. This drive is for experienced candidates; however, freshers can email their CVs for future openings.
Q4. What documents should candidates bring?
A4. Candidates must bring an updated resume, educational certificates, latest salary slips, and ID proof.
Q5. Can candidates apply online?
A5. Yes, resumes can be emailed to hr1@innoxells.com if unable to attend the walk-in.
| Company | Innoxel Lifesciences Pvt. Ltd. |
|---|---|
| Vacancies | QA, QC, Production, Microbiology, Project Management, Warehouse |
| Required Education | B.Sc, M.Sc, B.Pharm, M.Pharm, ITI, Diploma, B.Com |
| Experience | 1–10 Years (Sterile / USFDA Facility) |
| Location | Vadodara, Gujarat |
