Sr. Executive / Assistant Manager – Quality Assurance (QA)
at
SAVA Healthcare Limited
,
Surendranagar Plant
:
Job Title:
Sr. Executive / Assistant Manager – Quality Assurance (QA)
Location:
SAVA Healthcare Limited, Surendranagar Plant, Gujarat
Department:
Quality Assurance
Reports To:
QA Manager / Head – Quality
About SAVA Healthcare Limited
SAVA Healthcare Limited (SHL), established in 2003, is a diversified pharmaceutical company with a strong presence in International Business, Animal Healthcare, Herbal Products, and Contract Research & Manufacturing Services (CRAMS). With a vision to make life “Feel Good,” SHL is committed to delivering quality-driven pharmaceutical solutions globally.
Job Purpose:
To ensure the implementation and maintenance of cGMP practices, quality systems, and compliance with regulatory requirements at the Surendranagar plant. The role involves oversight of QA activities including documentation, validations, audits, and shop floor compliance to ensure product quality and regulatory adherence.
Key Responsibilities:
Ensure compliance with cGMP, SOPs, and regulatory requirements on the manufacturing floor.
Review and approve batch manufacturing records (BMRs) and batch packing records (BPRs).
Handle deviations, change controls, CAPA, and quality risk management activities.
Conduct self-inspections and support external/internal audits (regulatory, customer, corporate).
Review and approve SOPs, protocols, and reports related to validation, qualification, and quality systems.
Monitor and support process validation, cleaning validation, equipment qualification, and other validation activities.
Oversee document control, issuance, archival, and retrieval of QA-related documents.
Ensure timely closure of audit observations and CAPA implementation.
Coordinate with production, QC, warehouse, and other departments to ensure overall GMP compliance.
Participate in training programs and provide QA training to cross-functional teams.
Desired Candidate Profile:
Education:
B.Pharm / M.Pharm / M.Sc.
Experience:
4 to 7 years of experience in QA in a regulated pharmaceutical formulation plant.
Knowledge:
Strong understanding of GMP guidelines, quality systems, validation practices, and regulatory audits.
