Quality Control Analyst

at  Centre for Process Innovation

ABOUT CPI

CPI helps make great ideas and inventions a reality. We’re a team of intelligent people using advances in science and technology to solve the biggest global challenges in healthcare and sustainability.
Through our incredible people and innovation infrastructure, we collaborate with our partners in industry, academia, government, and the investment community to accelerate the development and commercialisation of innovative products.
From health technologies and pharmaceuticals to sustainable food and materials innovations, we turn the entrepreneurial spirit and radical thinking of our people and partners into incredible impact that makes our world a better place.

WHY THIS ROLE IS IMPORTANT FOR CPI’S WORK

CPI has an opportunity for a Quality Control Analyst to join the growing Quality team based at our Biologics RNA Centre of Excellence in Darlington.
The QC Analysts provide wide ranging quality control support to the quality function, promoting and integrating quality into every aspect of our business. In this role, you will perform a variety of tasks in support of specific areas of the site quality control function mainly focusing on the development, sustainability and continued improvement of the CPI Biologics quality control function to meet GMP requirements.
Projects within CPI encompass a broad range of process technologies, novel measurement and analytical techniques, this is reflected in the diversity of customers and their expertise. This role requires an expertise in biological analysis techniques with the ability to support in the validation of methods for use in the QC laboratory as well as providing training for colleagues.
Click here for more about the RNA Centre of Excellence

KEY RESPONSIBILITIES –

Key tasks in the QC Analyst role will include (but are not limited to the below), please download the job description for full details available on the CPI careers page:

• To maintain consistent and documented compliance with all relevant Safety, Health and Environment (SHE), Good Manufacturing Practice (GMP), Data Integrity (DI), quality and best practice requirements
• To perform laboratory work and data analysis in a timely manner and to a high standard.
• To perform laboratory investigations and out of specification investigations to GMP standards.
• To perform method development and method validation activities.
• To perform the required release activities for raw materials and critical consumables
• To review and approve risk assessments and validation documentation as required.
• To support the site Quality Management System including input into investigations and/or CAPAs.