Are you a seasoned quality assurance professional with a passion for excellence in the pharmaceutical industry? Puerto Life Sciences Pvt. Ltd., a leader in manufacturing high-quality sterile drugs (SVP & LVP), is hiring a Senior Quality Assurance Expert to join our team in Ghiloth, Neemrana, Rajasthan. This is your chance to contribute to innovation, compliance, and patient safety in a dynamic, growth-oriented environment. If you have experience in the sterile industry and a drive to uphold Good Manufacturing Practices (GMP), we want to hear from you!
Job Responsibilities
As a Senior Quality Assurance Expert (Manager/Assistant Manager/Senior Executive), you will play a pivotal role in maintaining and enhancing our quality standards. Your key responsibilities include:
- Ensuring GMP compliance by thoroughly reviewing Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).
- Overseeing line clearance and conducting In-Process Quality Assurance (IPQA) checks.
- Managing deviation handling, document control, and Quality Management System (QMS) elements like Corrective and Preventive Actions (CAPA) and change control.
- Coordinating internal and external audits to uphold regulatory standards.
- Supporting training programs and validation processes to ensure operational excellence.
Qualifications
To excel in this role, you should bring:
- Experience: 4+ years for Senior Executive, 6+ years for Assistant Manager, or 8+ years for Manager roles in the sterile pharmaceutical industry.
- Proven expertise in GMP compliance, QMS, CAPA, change control, and audit coordination.
- Strong knowledge of sterile drug manufacturing processes (SVP & LVP).
- Excellent attention to detail, problem-solving skills, and a proactive approach to quality assurance.
- Bachelor’s or Master’s degree in Pharmacy, Chemistry, or a related field.
Benefits
Joining Puerto Life Sciences offers:
- Competitive salary range: ₹6,00,000 – ₹12,00,000 per annum, based on experience.
- Opportunities for professional growth in a leading sterile drug manufacturing company.
- Collaborative and innovative work environment focused on patient safety.
- Access to training and development programs to enhance your skills.
How to Apply
Ready to elevate quality standards with Puerto Life Sciences? Please submit your resume, current CTC, and notice period to hr@puerto.in. Only candidates with sterile industry experience will be considered. Apply by October 07, 2025, to seize this opportunity!
FAQs
Q: What specific experience is required for this role?
A: Candidates must have 4-8+ years of experience in the sterile pharmaceutical industry, with expertise in GMP compliance, QMS, and sterile drug manufacturing processes.
Q: Where is the job located?
A: The position is based in Ghiloth, Neemrana, Rajasthan, at Puerto Life Sciences’ state-of-the-art facility.
