Job Overview
| Particulars | Details |
|---|---|
| Position | Multiple Openings Pharma |
| Company | Innoxel Life Sciences Private Limited |
| Location | Vadodara |
| Job Type | Full-Time |
| Experience | Fresher |
| Category / Department | Pharma |
| Application Mode |
🏢 About Innoxel Life Sciences Private Limited
Innoxel Life Sciences Private Limited is an emerging pharmaceutical manufacturing company headquartered in Vadodara, Gujarat, specializing in injectable vials and prefilled syringes. The company operates dedicated manufacturing blocks for general and potent products and has implemented advanced barrier technology, software-based process controls, and 21 CFR Part 11 compliant systems. With a growing team of scientific, engineering, manufacturing, and quality professionals, Innoxel is committed to delivering high-quality pharmaceutical products while maintaining global regulatory standards.
Company Address
Innoxel Life Sciences Private Limited
Survey No. 534/1,
Village: Kotambi,
Near VCA Stadium,
Taluka: Waghodia,
Vadodara, Gujarat
💡 Editor's Note / Preparation Tip
• Highlight sterile manufacturing and injectable experience.
• Mention USFDA, GMP, and validation exposure.
• Include analytical instruments and laboratory techniques.
• Quantify project achievements wherever possible.
• Keep your resume concise and ATS-friendly.
Interview Preparation
• Revise GMP, GLP, and USFDA guidelines.
• Prepare for department-specific technical questions.
• Review sterile manufacturing processes.
• Understand documentation and compliance practices.
• Be ready to discuss previous pharmaceutical projects.
Professional Tips
• Stay updated on current pharmaceutical regulations.
• Strengthen documentation and compliance skills.
• Demonstrate a quality-first mindset.
• Showcase problem-solving and teamwork abilities.
• Continue learning new manufacturing technologies.
📝 Job Description
🚀 Walk-In Interview Drive | Innoxel Life Sciences Private Limited
Looking to build or advance your career in the pharmaceutical manufacturing industry? Innoxel Life Sciences Private Limited is conducting a Walk-In Interview Drive for multiple departments at its state-of-the-art injectable manufacturing facility in Vadodara, Gujarat. Professionals with sterile manufacturing and USFDA exposure are encouraged to attend.
Position Details
🏢 Company: Innoxel Life Sciences Private Limited
💼 Departments & Roles:
- Quality Control – Officer / Sr. Officer / Executive / Sr. Executive (Analytical Method Validation & HPLC)
- Sterile / Liquid Oral Manufacturing – Operators / Officers / Executives (SKID Operation, Autoclave, Vial Washing, Tunnel, Manufacturing, Filling)
- QC Micro – Microbiologists (EM & Analysts)
- Quality Assurance – Dy. Manager / Sr. Executive / Executive / Officer (Compliance, Qualification & Validation, IPQA, Skilled Media Fill, CSV, QA of QC, AMV, Regulatory Affairs, Training Coordinator)
- Warehouse – Operator / Officer / Executive
- Engineering – Technician / Operator / Officer / Executive (Plant Maintenance, QMS, Utility & Water System, Civil)
- Project Management – Assistant Manager
- MS&T – Sr. Officer / Executive
- Validation – Sr. Officer / Executive
📍 Location: Vadodara, Gujarat
📄 Employment Type: Full-Time
🚶 Interview Type: Walk-In Interview
📅 Walk-In Date: 26 July 2026 (Sunday)
🕙 Walk-In Time: 10:00 AM – 4:00 PM
Preferred Skills
✔ Analytical Method Validation
✔ IPQA
✔ CSV
✔ Regulatory Affairs
✔ CAPA & Investigation
✔ Engineering Utilities
✔ Water System Knowledge
✔ Media Fill Experience
✔ Pharmaceutical Manufacturing Experience
Candidate Requirements
Quality Control
- Experience: 2–8 Years
- Qualification: B.Sc. / M.Sc. / B.Pharm / M.Pharm (Chemistry)
- Sterile USFDA experience preferred.
Sterile / Liquid Oral Manufacturing
- Experience: 1–8 Years
- Qualification: ITI / Diploma (Operators) or B.Pharm / M.Pharm (Officers & Executives)
- Sterile USFDA experience preferred.
QC Micro
- Experience: 1–5 Years
- Qualification: B.Sc. / M.Sc. Microbiology
- Sterile USFDA experience preferred.
Quality Assurance
- Experience: 2–14 Years
- Qualification: B.Pharm / M.Pharm / M.Sc.
- Sterile USFDA experience preferred.
Warehouse
- Experience: 0–6 Years
- Qualification: ITI / B.Sc. / B.Com.
- Sterile USFDA experience preferred.
Engineering
- Experience: 1–10 Years
- Qualification: ITI (Technicians & Operators), Diploma / B.E. (Supervisory Staff)
Project Management
- Experience: 6–10 Years
- Qualification: M.Pharm
- Relevant Injectable experience required.
MS&T
- Experience: 4–8 Years
- Qualification: B.Sc. / M.Sc. / B.Pharm
- Sterile USFDA experience preferred.
Validation
- Experience: 3–7 Years
- Qualification: B.Pharm / M.Pharm
- Sterile USFDA experience preferred.
Why Join Innoxel Life Sciences?
• Work in a modern injectable manufacturing facility.
• Exposure to advanced barrier technology and automated manufacturing systems.
• Opportunity to work in a USFDA-focused environment.
• Excellent learning and career development opportunities.
• Collaborative and quality-driven workplace.
• Exposure to regulatory inspections and global quality standards.
• Growing pharmaceutical organization with expansion opportunities.
How to Apply
🚶 Walk-In Venue:
Innoxel Life Sciences Private Limited
Survey No. 534/1, Village Kotambi,
Near VCA Stadium,
Taluka Waghodia,
Vadodara, Gujarat
📅 Date: 26 July 2026 (Sunday)
🕙 Time: 10:00 AM – 4:00 PM
📧 Unable to attend? Send your resume to: hr1@innoxells.com
Know someone who would be a great fit? Tag them or share this opportunity with your network!
🎯 Key Responsibilities
- ✓ Execute department-specific manufacturing, quality, engineering, validation, or warehouse activities.
- ✓ Ensure compliance with USFDA, GMP, SOPs, and quality standards.
- ✓ Perform analytical testing and laboratory activities where applicable.
- ✓ Handle sterile manufacturing operations and production equipment.
- ✓ Maintain accurate documentation and batch records.
- ✓ Support validation, qualification, and compliance activities.
- ✓ Collaborate with cross-functional teams to achieve production and quality goals.
- ✓ Follow safety procedures and regulatory guidelines.
- ✓ Contribute to continuous improvement initiatives.
💡 Required Qualifications & Skills
🚀 Career Guidance & Interview Insights
To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.
This Multiple Openings Pharma role is a chance to contribute directly to life sciences, patient care, or pharmaceutical advancements. You will work within strict compliance frameworks, ensure rigorous quality standards, and collaborate with technical or medical experts. It is a career path that blends scientific excellence with a deep sense of social purpose.
Healthcare and pharmaceutical professionals grow through specialized scientific experience. Entry-level starts as Lab Technician, Chemist, or Quality Associate, progressing to Senior QA/QC Analyst. Advancement leads to Lab Supervisor, Clinical Project Manager, and senior management roles like Quality Director, VP of Regulatory Affairs, or Chief Scientific Officer.
Expected Technical & Behavioral Questions:
- Q1: How do you ensure compliance with WHO/GMP guidelines during laboratory operations?
Answer Tip: Mention strict adherence to Standard Operating Procedures (SOPs), detailed batch records, regular equipment calibration, and sanitization cycles. - Q2: What steps do you take when a quality deviation is detected in a product batch?
Answer Tip: Outline immediate isolation of the batch, raising a deviation report, root cause analysis (RCA), and initiating CAPA (Corrective and Preventive Action). - Q3: How do you manage safety protocols while handling toxic chemicals?
Answer Tip: Discuss using Material Safety Data Sheets (MSDS), wearing appropriate Personal Protective Equipment (PPE), proper ventilation, and chemical spill kits.
To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:
- Keywords to include: Quality Control (QC), GMP Compliance, FDA Regulations, SOP Documentation, HPLC/GC analysis, Batch Validation, Clinical Trials, Pharmacovigilance.
- Format: List laboratory skills and instruments handled (e.g. HPLC, spectrophotometer) in a dedicated technical matrix.
- Quantify Results: E.g., 'Validated 15 batch formulations under GMP guidelines with zero quality defects.'
Estimated compensation for this role type in India is ₹2,40,000 - ₹3,80,000 per annum (Fresher analyst). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.
Key credentials: GMP Certified Professional (ASQ), Certified Clinical Research Coordinator (CCRC), or specialized laboratory training certificates in high-performance liquid chromatography (HPLC) and safety standards.
Frequently Asked Questions
Q1. When is the walk-in interview?
26 July 2026 (Sunday).
Q2. What are the interview timings?
10:00 AM – 4:00 PM.
Q3. Can I apply if I cannot attend the walk-in?
Yes. Candidates who are unable to attend may email their resumes to hr1@innoxells.com.
Q4. Is sterile manufacturing experience preferred?
Yes. Most positions prefer candidates with Sterile USFDA experience.
Q5. Which departments are hiring?
Quality Control, Manufacturing, QC Microbiology, Quality Assurance, Warehouse, Engineering, Project Management, MS&T, and Validation.
Share This Job
🛡️ Safety Disclaimer: JobPortalConnect curates official listings for informational purposes. Genuine recruiters will never ask you for processing fees, training payments, or security deposits. If you spot suspicious activity, copyright issues, or wish to request the removal of this listing, please report it to us immediately at contact.jobportalconnect@gmail.com.