Company Description Stavros Pharmaceuticals Pvt. Ltd. is a new-age pharmaceutical company with a vision to become a global healthcare leader through quality and innovation. The organization focuses on scientific excellence and continuous innovation to deliver breakthrough healthcare solutions.

A dedicated team works to address the evolving needs of patients, healthcare professionals, and the wider medical community. Every product is developed to meet the highest quality standards and reflect the latest advances in science and technology. This robust commitment to research, development, and improving lives positions Stavros as an emerging trailblazer in the pharmaceutical industry.

Role Description The QA Lead – Injectable Manufacturing is responsible for overseeing all quality assurance activities related to sterile injectable products in a WHO-GMP and cGMP-compliant manufacturing environment. Day-to-day responsibilities include establishing and maintaining quality systems, reviewing and approving batch manufacturing records, ensuring adherence to SOPs, and driving compliance with regulatory and company standards. The role involves leading quality investigations, managing CAPA, coordinating validation activities, and supporting internal and external audits.

The QA Lead will collaborate closely with production, QC, regulatory, and engineering teams to ensure consistent product quality and continuous improvement. This is a full-time, on-site position based at the injectable manufacturing facility in Baddi,



Himachal Pradesh.

Qualifications

- Candidates should possess strong Quality Assurance skills, including experience in pharmaceutical QA for injectable manufacturing and quality system implementation.
- Candidates should possess Quality Control and Quality Management skills to oversee testing standards, manage quality metrics, and support overall QMS effectiveness.
- Candidates should possess Good Manufacturing Practice (GMP), WHO-GMP, and cGMP compliance skills to ensure adherence to global regulatory requirements and site procedures.
- Candidates should possess Quality Auditing skills, including participation in internal audits, vendor audits, and readiness for regulatory inspections.
- 12+ years of progressive pharma QA experience in sterile/injectable manufacturing, with proven leadership in QA teams.
- Educational qualifications: B.Pharm, M.Pharm, or M.Sc in a relevant scientific discipline.
- Hands-on experience with validation (process, cleaning, equipment, and utilities), change control, deviation handling, and CAPA management.
- Strong knowledge of QMS, documentation practices, data integrity principles, and regulatory compliance guidelines.
- Effective communication, stakeholder management, and team leadership skills, with the ability to train and mentor QA and operations personnel.
- Ability to work on-site in Baddi, Himachal Pradesh, and collaborate cross-functionally in a dynamic manufacturing environment.

📌 QA Sr Manager – Injectable Manufacturing | 12+ Years Pharma QA Experience | B.Pharm/M.Pharm/M.Sc | WHO-GMP, cGMP, QMS, Validation & Regulatory Compliance | Baddi, Himachal Pradesh
🏢 Stavros Pharmaceuticals
📍 Baddi