Are you passionate about ensuring world-class quality in sterile pharmaceutical manufacturing? Puerto Life Sciences Pvt. Ltd., a leader in sterile product innovation, is hiring for Quality Assurance (QA) jobs in 2025. Based in India, Puerto is seeking dedicated professionals to join their mission of delivering excellence in sterile manufacturing. Whether you’re an experienced QA Manager, Executive, or Officer, these roles offer a chance to drive quality, compliance, and innovation in a dynamic environment. Explore the opportunities below and apply today to shape the future of pharmaceutical quality assurance.
Job Roles and Responsibilities
1. Manager / Assistant Manager / Deputy Manager (QA)
- Experience: 8–15 years in sterile manufacturing
- Oversee end-to-end compliance with global quality standards (e.g., USFDA, WHO, GMP).
- Lead internal and external audits, ensuring regulatory readiness.
- Manage documentation for Quality Management Systems (QMS) and compliance.
- Drive cross-functional QA initiatives to enhance product quality.
- Mentor QA teams to foster excellence and continuous improvement.
2. Executive / Senior Executive (QMS, IPQA, Validation)
- Experience: 5–8 years in sterile manufacturing
- Execute QMS activities with precision, ensuring regulatory compliance.
- Support In-Process Quality Assurance (IPQA) operations on the shop floor.
- Conduct validation processes for equipment, processes, and systems.
- Contribute to robust documentation and quality improvement initiatives.
- Collaborate with cross-functional teams to maintain sterile product standards.
3. Officer / Senior Officer (QA)
- Experience: 2–5 years in sterile manufacturing
- Assist in QMS documentation and ensure regulatory compliance.
- Perform IPQA checks and support validation activities.
- Ensure adherence to standard operating procedures (SOPs).
- Maintain quality consistency across production processes.
- Support senior QA staff in audits and compliance tasks.
Qualifications
- Education: B.Pharm, M.Pharm, or relevant life sciences degree.
- Experience: Exclusive experience in sterile pharmaceutical manufacturing (injectables, vials, or similar).
- Skills:
- Strong knowledge of global regulatory standards (USFDA, WHO, GMP).
- Expertise in QMS, IPQA, and validation processes.
- Excellent documentation and analytical skills.
- Leadership and mentoring abilities (for Manager roles).
- Certifications: Relevant certifications in quality assurance or regulatory affairs are a plus.
Benefits of Working at Puerto Life Sciences
- Competitive Salary: INR 4,00,000–15,00,000 per annum, based on role and experience.
- Career Growth: Opportunities to lead high-impact QA projects and grow within a reputed organization.
- Work Environment: Collaborative, innovative, and focused on quality excellence.
- Training & Development: Access to continuous learning and professional development programs.
- Health & Wellness: Comprehensive health benefits and wellness initiatives.
How to Apply
Ready to join Puerto Life Sciences? Send your resume, current CTC, and notice period to hr@puerto.in. Ensure your application highlights your sterile industry experience, as only candidates with relevant expertise will be considered. Applications are reviewed on a rolling basis—apply by October 20, 2025, for priority consideration.
FAQs
Q: What type of experience is required for these QA roles?
A: Puerto Life Sciences seeks candidates with exclusive experience in sterile pharmaceutical manufacturing, such as injectables or vials, to ensure compliance with global standards.
Q: How soon can I expect a response after applying?
A: Shortlisted candidates will be contacted within 2–3 weeks of application submission, depending on the volume of applications.
