Are you a skilled pharmaceutical professional seeking a rewarding career? Pinnacle Life Science Pvt. Ltd., a 100% subsidiary of Aarti Drugs Ltd., is hiring for AQA (Analytical Quality Assurance) and IPQA (In-Process Quality Assurance) roles at its state-of-the-art formulation (OSD) plant in Baddi, Himachal Pradesh. As one of India’s fastest-growing pharmaceutical companies, Pinnacle operates in over 70 countries with approvals from PIC/S, USFDA, MHRA, and WHO. Join a team of over 2,000 professionals driving innovation and excellence in the pharmaceutical industry.
This article details the AQA and IPQA job vacancies in Baddi, including responsibilities, qualifications, benefits, and how to apply. Whether you’re an experienced professional or an aspiring officer, these roles offer a chance to grow with a globally recognized leader.
Job Responsibilities
AQA (Executive / Sr. Officer / Officer)
- Conduct quality control testing using QC instruments to ensure product compliance.
- Utilize Empower and Lab Solutions software for accurate data analysis.
- Perform online and offline data review to maintain quality standards.
- Ensure adherence to regulatory guidelines (PIC/S, USFDA, MHRA, WHO).
- Implement QMS (Quality Management System) practices for operational excellence.
- Support regulatory audits with thorough documentation and compliance.
IPQA (Sr. Officer / Officer)
- Monitor in-process quality checks during formulation (OSD) production.
- Ensure compliance with regulatory guidelines and internal SOPs.
- Maintain QMS practices to uphold manufacturing standards.
- Conduct real-time data reviews and resolve quality deviations.
- Collaborate with cross-functional teams to support audit readiness.
Qualifications and Skills
AQA (Executive / Sr. Officer)
- Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
- Experience: 5-7 years in pharmaceutical quality assurance
- Skills:
- Proficiency in QC instruments and analytical testing
- Expertise in Empower and Lab Solutions software
- Strong knowledge of online and offline data review
- Familiarity with regulatory guidelines (USFDA, MHRA, WHO, PIC/S)
- Working knowledge of QMS practices
- Regulatory audit exposure
AQA (Officer)
- Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
- Experience: 2-4 years in pharmaceutical quality assurance
- Skills: Same as above, with foundational experience
IPQA (Sr. Officer / Officer)
- Qualification: B.Pharm / M.Pharm
- Experience: 3-5 years in in-process quality assurance
- Skills:
- Strong understanding of formulation (OSD) processes
- Knowledge of regulatory compliance and QMS
- Experience in real-time quality monitoring
- Regulatory audit exposure
Benefits of Working at Pinnacle Life Science
- Global Exposure: Work with a company operating in 70+ countries.
- Career Growth: Opportunities for professional development in a top-tier pharmaceutical firm.
- Competitive Salary: Attractive compensation (₹4,00,000–₹8,00,000 annually, based on experience).
- Work Environment: Join a dynamic team at a USFDA, MHRA, and WHO-approved facility.
- Stability: Be part of a subsidiary of Aarti Drugs Ltd., a trusted name in pharmaceuticals.
How to Apply
Interested candidates can send their updated resume to Ms. Varsha (HR) at Pinnacle Life Science Pvt. Ltd. Ensure your application highlights relevant experience in pharmaceutical quality assurance, QC instruments, and regulatory audits.
Contact Details:
- Address: Pinnacle Life Science Pvt. Ltd., Vill. Manpura, Tehsil Baddi, Distt. Solan, Himachal Pradesh – 174101
- Email: Include a professional email (e.g., hr@pinnacelifescience.com) or check Pharmabharat.com for updates.
- Application Deadline: October 19, 2025
Visit Pharmabharat.com for more details and to submit your application online.
FAQs
1. What is the salary range for AQA and IPQA roles at Pinnacle Life Science?
The salary for AQA and IPQA positions ranges from ₹4,00,000 to ₹8,00,000 per annum, depending on experience and role (Executive, Sr. Officer, or Officer).
2. What qualifications are required for the Baddi job openings?
Candidates need a B.Sc, M.Sc, B.Pharm, or M.Pharm with 2–7 years of experience in pharmaceutical quality assurance, depending on the role.
