Senior QC Analyst

PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.

Employees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development through learning & development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client’s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.

The Senior QC Analyst is responsible for supporting GMP-compliant laboratory operations, ensuring efficient QC testing, and partnering cross-functionally to maintain the highest standards of quality, safety, and compliance. This position requires strong microbiology experience and a solid background in pharmaceutical quality systems. The successful candidate will play a key role in ensuring material release, laboratory compliance, audit readiness, and continuous improvement initiatives across site operations.

Key Responsibilities:

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• Perform GMP-compliant laboratory testing and support QC material release and scheduling activities
  
• Support and deliver on QC Key Performance Indicators (KPIs)
  
• Participate actively in QC documentation review and approval processes
  
• Maintain and support laboratory equipment and utilities in compliance with GMP requirements
  
• Partner cross-functionally to ensure all QC testing xcfaprz activities are completed efficiently
  
• Contribute to QC training initiatives, supporting both personal competency and team development
  
• Support internal and external audits, ensuring inspection readiness at all times
  
• Drive continuous improvement initiatives aligned with departmental goals and objectives
  
• Maintain and develop expertise in analytical methods, microbiological techniques, laboratory technologies, and evolving compliance requirements
  
• Comply with all EHS procedures and foster a culture of safety, quality, and Credo-based behaviours across the site