Job Description
CY Partners are excited to be working with a global pharmaceutical company to offer a fantastic new opportunity for a Quality Analyst to join their high-performing Quality Laboratory team. This role is a great fit for someone with a background in analytical testing and a passion for working in a regulated, science-led environment. You’ll play a key part in delivering essential support services and ensuring products flow seamlessly through the site’s quality systems.
12 Month Contract, up to 32,000 p/a DOE
Role Responsibilities:
* Perform routine and non-routine analysis of raw materials, intermediates, finished products, and stability samples using classical and chromatographic techniques.
* Troubleshoot production issues by providing analytical support and problem-solving expertise.
* Ensure work is conducted in compliance with current Good Laboratory Practices (cGLP) and internal procedures.
* Contribute to laboratory operations through documentation preparation, procedure reviews, risk assessments, and continuous improvement initiatives.
* Support audits (GMP, 5S, self-inspections) and contribute to maintaining high standards across the lab.
* Use systems such as M-ERP and other IT platforms for data management and reporting.
* Take part in capability building by training colleagues and expanding personal expertise across analytical methods.
* Uphold safety and compliance procedures in all laboratory activities, supporting a culture of continuous improvement.
* Manage deviations, change control, and quality improvement actions in a timely and professional manner.
Key Requirements:
* Previous experience in a Quality Control laboratory or equivalent role within a regulated environment.
* Competency in a range of analytical techniques, including chromatography and classical tests.
* Strong understanding of cGLP and quality compliance within the pharmaceutical industry.
* Excellent communication skills and a collaborative mindset to work effectively across departments.
* Proficient in using lab-based IT systems and electronic data management tools.
* Demonstrated commitment to safety, quality, and continuous improvement.
* Ability to manage time effectively, prioritize tasks, and meet site quality metrics.
* Experience supporting audits and laboratory inspections.