Job Description

Job Summary:

We are looking for a detail-oriented and proactive Quality Assurance Executive to join our team. The ideal candidate will be responsible for managing the quality assurance and documentation processes across departments including R&D, Production, and Quality Control. The role will also support SOP preparation, implementation, and regulatory audit documentation, ensuring compliance with industry standards and company policies.

Key Responsibilities:

Oversee and maintain QA documentation related to R&D, Production, and Quality Control departments. Draft, review, and update Standard Operating Procedures (SOPs) in alignment with regulatory and organizational requirements. Ensure compliance with GMP, GLP, and other regulatory guidelines applicable to the factory operations. Support the preparation and coordination of regulatory audits and inspections by maintaining accurate records and documentation. Conduct internal audits, identify gaps, and follow up with corrective and preventive actions (CAPA). Collaborate with cross-functional teams to ensure quality compliance and continuous improvement. Provide training and support to team members on QA processes, SOPs, and documentation practices. Maintain and track quality metrics, ensuring timely reporting and escalation where necessary.
Key Requirements:

Bachelor's/Master's degree in Chemistry, Microbiology, Pharmacy, or related field. Minimum 1-3 years of experience in QA within the chemical, pharmaceutical, or specialty chemical industry. Strong knowledge of quality systems, documentation practices, and regulatory requirements. Experience in handling regulatory audits and compliance-related activities. Excellent communication, organizational, and analytical skills. Proficiency in MS Office and familiarity with ERP/QA documentation systems will be an added advantage.
Job Types: Full-time, Permanent

Pay: ₹300,000.00 - ₹350,000.00 per year

Benefits:

Provident Fund
Work Location: In person