Overview:
The In-Process Quality Assurance (IPQA) Executive will be responsible for ensuring product quality during various stages of the manufacturing process. This role plays a critical part in maintaining compliance with cGMP, SOPs, and regulatory standards. The candidate will work closely with manufacturing, quality control, and cross-functional teams to ensure the delivery of high-quality and compliant products.
Responsibilities:
Monitor in-process activities to ensure adherence to defined quality standards and SOPs.
Perform line clearance, online sampling, and verification during manufacturing and packing processes.
Record deviations and non-conformities observed during operations and support in investigations.
Review batch manufacturing records (BMR) and ensure real-time documentation.
Ensure implementation of GMP practices on the shop floor.
Participate in internal audits, regulatory inspections, and CAPA implementations.
Support qualification and validation processes of equipment, facilities, and processes.
Coordinate with production and QC teams for timely resolution of quality issues.
Skills Required:
2 to 5 years of hands-on IPQA experience in Pharma or FMCG manufacturing units.
Sound knowledge of cGMP, GDP, and regulatory requirements (FDA, WHO, etc.).
Strong observational skills and attention to detail during in-process checks.
Good documentation practices and familiarity with BMR/BPR review.
Ability to work effectively in a team and handle pressure during audits.
Proficient in MS Office and quality documentation tools.
Excellent communication and coordination skills.
