Lonza hiring pharmacy graduates | QA specialist role
Lonza careers present a rare opportunity for experienced professionals in Quality Assurance in Hyderabad, India. The organization is seeking a Senior QA Specialist specializing in QA Documentation with 3–7 years of relevant experience. This opportunity involves critical responsibilities in GMP documentation and compliance.
About Lonza
Lonza is a global life sciences organization supporting the development and manufacturing of medicines and therapies. With more than 30 sites across five continents, Lonza’s globally connected teams collaborate to help transform scientific ideas and customer innovations into viable therapies. The organization emphasizes core values such as collaboration, accountability, excellence, passion, and integrity, operating across the pharmaceutical, biotechnology, and life sciences ecosystem.
Company: Lonza
Job Title: Senior QA Specialist – QA Documentation
Department: Quality Systems & Compliance
Job Requisition ID: R75352
Location: Hyderabad, India
Employment Type: Full-Time
Experience: 3–7 years
Industry: Pharmaceutical / Biotechnology / Life Sciences
Posted: 09 September 2026
Lonza Careers: Job Description
The Senior QA Specialist – QA Documentation will be responsible for the compliant management and oversight of quality documentation throughout its lifecycle. This Lonza careers opportunity focuses on ensuring that GMP-relevant documents are properly managed from finalization through archiving, customer dispatch, retention, or destruction. The QA specialist will also act as a key decision-maker for documentation lifecycle activities and serve as the QA representative for archiving processes.
Key Responsibilities
- Provide Quality Assurance oversight for GMP and quality-relevant documentation.
- Manage documentation from finalization through dispatch, archiving, retention, or destruction.
- Ensure compliance with internal Standard Operating Procedures (SOPs).
- Maintain documentation integrity and traceability.
- Support regulatory and customer requirements.
- Optimize the True Copy Scanning process and maintain related SOPs.
- Act as the QA representative for archiving activities.
- Evaluate retain samples that exceed defined retention periods.
Senior QA Specialist Eligibility Criteria
- B.Pharm, M.Pharm, Pharm.D, Biotechnology, Microbiology, Chemistry, or other relevant Life Sciences qualifications.
- Experience in Quality Assurance and Documentation Management within highly regulated environments.
- Strong understanding of GMP requirements, GxP regulations, and Data Integrity principles.
Required Skills
- Strong decision-making abilities and risk assessment skills.
- Excellent attention to detail and strong organizational abilities.
- Effective communication skills and stakeholder management.
- Ability to manage complex retention schedules.
- Knowledge of electronic records and regulated computerized systems.
Salary
Lonza has not disclosed the official salary for Job Requisition R75352. Based on comparable Senior QA Specialist and QA Documentation roles in Hyderabad’s pharmaceutical and biotechnology industry, the estimated annual salary range may be: ₹8,00,000 – ₹15,00,000 per annum. Note: This is an editorial estimate based on comparable roles and is not an official Lonza salary disclosure. Actual compensation may depend on experience, qualifications, technical expertise, internal compensation structures, and other factors. Candidates should confirm compensation details during the recruitment process.
How to Apply
CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
Conclusion
For candidates pursuing Lonza careers, this position presents a significant opportunity to advance in Quality Assurance and documentation management within a global life sciences organization. Interested individuals are encouraged to apply at the earliest before the deadline.
