Purpose: To establish, implement, and maintain a robust Quality Assurance system ensuring that all products, processes, and operations comply with internal standards, customer requirements, and applicable regulatory guidelines.

Key Responsibilities:

- Develop, implement, and maintain the Quality Management System in line with ISO standards.

- Ensure compliance with documentation control, change management, and record retention systems.

- Ensure Data Integrity & lead implementation of Digital Quality Systems

- Quality matrices and KPI management

- Supplier quality management

- Review and approve batch manufacturing records, process deviations, and change controls. Ensure adherence to approved specifications, process parameters, and quality plans.

- Lead investigations for deviations, non-conformances, and customer complaints. Perform root cause analysis (RCA) and ensure timely implementation of CAPA.

- Lead and coordinate customer, ISO, and regulatory audits. Ensure timely closure of audit observations and preventive actions.





- Plan and conduct internal quality audits.

- Ensure integrity, accuracy, and traceability of quality documents and records.

- Train employees on quality systems, SOPs, and compliance requirements.

Competencies:

- Good understanding of specialty chemical manufacturing processes.

- Solid analytical and problem-solving skills.

- Expertise in deviation management, RCA, CAPA, and audit handling.

- Leadership and team management skills.

- Strong documentation, compliance, and data integrity mindset.

- Effective communication and coordination skills.

- Ability to work under pressure in a fast-paced chemical production environment.

Qualification: M.Sc./ Ph.D.

- Chemistry

Nature of Experience:

- 10 to 15 years of Quality Assurance experience in specialty chemicals / fine chemicals / intermediates / process chemicals, and in the capacity of QA Incharge for at least 3 years.

📌 Manager - Quality Assurance (QA) (Visakhapatnam)
🏢 Novopor Advanced Science
📍 Visakhapatnam