Are you a passionate pharmaceutical professional looking to advance your career in a dynamic, innovative environment? Innoxel Lifesciences, a leading name in the pharmaceutical industry, is hiring a Stability Coordinator in Vadodara, Gujarat. This role offers an exciting opportunity to contribute to high-quality drug development while ensuring compliance with global standards like ICH and cGMP. If you have a B.Pharm degree and 2-5 years of experience in a USFDA-approved injectable plant, this could be your next career move!
Key Responsibilities
As a Stability Coordinator at Innoxel Lifesciences, you will play a pivotal role in ensuring the quality and stability of pharmaceutical products. Your responsibilities will include:
- Designing and Executing Stability Studies: Plan and conduct stability studies for drug substances, products, and raw materials in line with ICH guidelines (Q1A-Q1F) and cGMP standards.
- Database Management: Maintain the stability program database, ensuring accurate sample tracking, data entry, and scheduling of time-point pulls.
- Collaboration with QC Labs: Coordinate with Quality Control (QC) teams to ensure timely testing of stability samples.
- Protocol and Report Generation: Draft and review stability protocols, summaries, and reports to meet regulatory requirements.
- Monitoring Storage Conditions: Oversee temperature and humidity controls in stability chambers, addressing any excursions or deviations promptly.
- Investigating OOS/OOT Results: Work with Quality Assurance (QA) and QC teams to investigate Out of Specification (OOS) or Out of Trend (OOT) results.
- Documentation: Maintain accurate and complete records of all stability-related activities to ensure regulatory compliance.
Qualifications
To excel in this role, candidates should meet the following criteria:
- Education: B.Pharm degree from a recognized institution.
- Experience: 2-5 years of experience in stability, QA, or QC roles within a USFDA-approved injectable plant.
- Skills:
- Strong knowledge of ICH guidelines (Q1A-Q1F) and cGMP standards.
- Proficiency in stability study design and execution.
- Excellent analytical and problem-solving skills for OOS/OOT investigations.
- Strong communication and collaboration skills for cross-functional teamwork.
- Attention to detail and proficiency in documentation.
Benefits of Joining Innoxel Lifesciences
Working with Innoxel Lifesciences offers a range of benefits, including:
- Career Growth: Opportunities to grow within a leading pharmaceutical company committed to innovation.
- Collaborative Environment: Work with a dynamic team of professionals in a USFDA-approved facility.
- Impactful Work: Contribute to the development of high-quality pharmaceutical products that improve lives.
- Competitive Salary: Attractive compensation package with a salary range of INR 4,00,000–6,00,000 per annum, based on experience.
How to Apply
Ready to take the next step in your pharmaceutical career? Submit your resume to vikrant.datta@innoxells.com or send it via WhatsApp to +91 89800 01454 (WhatsApp submissions only). Ensure your application highlights your relevant experience and qualifications. Applications are open until November 3, 2025. Don’t miss this opportunity to join Innoxel Lifesciences and make a difference in the pharma industry!
FAQs
What qualifications are required for the Stability Coordinator role?
Candidates must have a B.Pharm degree and 2-5 years of experience in stability, QA, or QC roles in a USFDA-approved injectable plant.
How can I apply for this position?
Send your resume to vikrant.datta@innoxells.com or via WhatsApp to +91 89800 01454. Ensure your application is submitted by November 3, 2025.
