Description

As a QA Manufacturing Lead, you will ensure product quality by overseeing manufacturing processes, monitoring compliance with GMP standards, and providing hands-on training to the team. This role involves real-time support, documentation review, and active participation in audits, making a significant impact on quality assurance.

Requirements

• •Strong background in quality assurance within pharmaceutical or regulated manufacturing environment
• •Solid understanding of GMP (Good Manufacturing Practices)
• •Good understanding of aseptic process and its core requirements
• •Excellent communication and coaching skills
• •Ability to make sound decisions and manage deviations in a fast-paced setting
• •Collaborative spirit and genuine passion for ensuring compliance and product integrity

Tasks

• •Provide real-time quality assurance support on the shop floor
• •Monitor adherence to GMP practices during critical manufacturing steps
• •Witness and verify critical process steps and in-process controls
• •Perform and document line clearances before manufacturing operations
• •Review manufacturing processes for compliance with approved batch records
• •Ensure proper material handling, labeling, and segregation during production
• •Identify and report deviations or abnormal events on the shop floor
• •Support or lead immediate impact assessments of on-the-floor deviations
• •Ensure timely escalation and coordination with QA and production leadership
• •Review completed batch manufacturing records for accuracy and compliance
• •Assist operators in proper GMP documentation practices
• •Verify logbooks, equipment use records, and cleaning records
• •Observe and assess interventions during aseptic operations for compliance
• •Support environmental monitoring activities and cleanroom behavior compliance
• •Conduct routine walkthroughs and spot checks for GMP standards
• •Participate in internal audits and regulatory inspections as needed
• •Provide on-the-job coaching and GMP guidance to operators and technicians
• •Reinforce good documentation practices and quality culture
• •Provide input into root cause analysis based on observations
• •Support implementation and follow-up of corrective and preventive actions

Benefits