Senior Quality Control Analyst

About PSC BiotechWho are we?

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.

‘Take your Career to a new Level’

PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting.

Employee Value Proposition

Employees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development though 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.

Role Overview

We are seeking an experienced Quality Control Analyst to join the Quality Control Department. This role 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

• 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 compliance across the site

Required Experience and Qualifications

• Third-level degree in a Science, Microbiology, Pharmaceutical Science, or related discipline
• Minimum of 3 years’ experience in a quality or compliance role within the pharmaceutical industry
• Strong hands-on microbiology laboratory experience is essential
• Experience in environmental monitoring, bioburden testing, endotoxin testing, sterility testing, or microbial identification is highly desirable
• Working knowledge of GMP regulations and pharmaceutical quality systems
• Experience supporting regulatory inspections and audits preferred

Key Skills and Competencies

• Builds strong, productive cross-functional relationships
• Demonstrates accountability for compliant and flawless execution
• Strong communication and documentation skills
• Ability to work effectively both independently and as part of a team
• Innovative mindset with a focus on continuous improvement
• Consistently demonstrates integrity and quality-focused decision-making