Company Overview
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.
Employee Value Proposition
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.
Overview
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.
Requirements
Key Responsibilities:
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 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
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