About PSC Biotech

Who 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.

Position Overview

The QC analyst works as directed by the QC Manager/QC Associate Director according to company safety policies, cGMP and cGLP. Ensure that QC team objectives are effectively achieved, consistent with requirements to ensure compliance, safety and reliable supply to our customers.

Requirements Responsibilities

• Operate as part of the QC team performing the allocated testing and laboratory-based duties.
• Act as testing SME with QC department, participate in OOS investigations and supporting troubleshooting activities.
• Participate in QC Tier daily meetings and ensure effective communication of testing progress, deviations, escalation of potential cGMP or compliance issues etc.
• Participate in writing/revising/ rolling out accurate operational procedures, training materials and maintenance procedures for various Quality systems.
• Peer review of testing documentation and ensuring data integrity compliance and QC Right First Time KPIs are achieved.
• Support activities including general lab readiness, audit readiness and audit participation, laboratory equipment qualification and analytical method technical transfer, verification and validation.
• Maintain laboratory equipment, cleaning and support vendor maintenance tasks.
• Carry out and execute CMMS tasks in conjunction with equipment maintenance.
• Contributing to a continuous improvement environment and bringing problem solving and troubleshooting capabilities.
• Demonstrating a commitment to learning and personal development.

Qualification

Degree qualification (Science/Quality/Technical). 2 years of laboratory experience, including sampling, testing, reporting.

Skills Requirements

• Motivation to be an inspiring member of a high performing team and passion to build the future of.
• Desire to continuously learn, improve and develop.
• Flexible and self-motivated.
• Possess effective communication and presentation skills.
• Proficient with IT e.g. Microsoft office.
• Good critical thinking and problem solving skills.
• Good knowledge of cGMP, GLP, Quality Management Systems.