Job Title: Senior QC Analayst Location: North West England Position Type: Full-Time Industry: Pharmaceutical Company Overview: The QC Analyst role is at a leading Pharmaceutical company in the North West of England, our client has a wide port folio of licenced and non-licenced products The site has significantly expanded over the years to increase production capacity and now are looking to recruit Quality analysts to support this expansion. Senior QC Analyst Responsibilities: • Conduct routine and non-routine analysis of finished pharmaceutical products using techniques such as HPLC (High-Performance Liquid Chromatography) in compliance with GMP (Good Manufacturing Practices) guidelines. • Perform method validation and transfer activities, ensuring all analytical methods meet regulatory and quality requirements. Preferable • Maintain accurate and detailed records of all analytical activities in laboratory notebooks and electronic systems, ensuring data integrity and traceability. • Analyse and interpret analytical data, identifying trends, deviations, and potential issues. Report and investigate any out-of-specification (OOS) results in accordance with company procedures. • Participate in laboratory investigations and CAPA (Corrective and Preventive Action) processes to ensure continuous improvement and compliance. • Support the development, validation, and implementation of new analytical methods and techniques to enhance laboratory capabilities and efficiency. • Collaborate with cross-functional teams, including R&D, Production, and Quality assurance, to ensure timely and effective resolution of quality issues and support product development initiatives. • Ensure compliance with all relevant regulatory requirements, including GMP, ICH (International Conference on Harmonisation), and FDA (Food and Drug Administration) guidelines. Qualifications and Experience: • Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related field. A master's degree is preferred. • Experience in a pharmaceutical QC laboratory, with a focus on finished product testing. • Proven experience with HPLC analysis • method development/validation experience is beneficial. • In-depth knowledge of quality requirements • experience working in a GMP-compliant environment preferential. • Strong analytical skills, attention to detail, and ability to interpret complex data. • Excellent written and verbal communication skills, with the ability to effectively document and report analytical findings. • Proficiency in using laboratory software and electronic data management systems. • Ability to work independently and as part of a team, with a proactive and solutions-oriented mindset. Benefits: • Competitive salary • Opportunities for professional development and career advancement. • A collaborative and supportive work environment. • Contribution to meaningful projects that impact patient health and well-being. Application Process: Interested candidates are invited to apply and should their skillset align with the position I will reach out directly to discuss the opening in more detail. Note:The client is unable to provide sponsorship