QC Lab Management Analyst

Description

Summary: Join as a QC Lab Management Analyst to ensure smooth laboratory operations and GMP compliance in a biopharmaceutical environment developing gene therapy products. Highlights: 1. Support development and manufacturing of life-changing gene therapy products 2. Contribute to continuous improvement initiatives and team meetings 3. Opportunity to impact therapies that improve people's lives **About the role:** Are you passionate about ensuring smooth laboratory operations in a cutting\-edge biopharmaceutical environment? Join us as a **QC Lab Management Analyst** and play a key role in supporting the development and commercial manufacturing of life\-changing gene therapy products. In this position, you will help maintain compliance with Good Manufacturing Practices (GMP), optimize lab resources, and contribute to delivering high\-quality products that make a real difference. **Key Tasks:** * Oversee and coordinate the availability of laboratory resources, including equipment, reagents, and consumables. * Maintain accurate inventory records and ensure timely procurement of supplies. * Support material receipt, storage, tracking, and disposal according to protocols. * Collaborate with the Engineering team to ensure equipment qualification, calibration, and maintenance. * Assist in preparing, reviewing, and maintaining FMRGs related to lab operations. * Work closely with QC analysts, scientists, and cross\-functional teams to ensure smooth operations. * Ensure compliance with regulatory guidelines and company quality standards. * Participate in internal and external audits. * Contribute to continuous improvement initiatives and team meetings. **Key Working Relation:** * Quality departments **Skills \& Qualifications:** * Education: Higher Degree in Qualiy Control, Laboratory or similar. * Previous experience of 1 year in lab management within the biopharmaceutical or biotech industry. * Familiarity with bioanalytical methods for gene therapy products. * Level of English to be able to perform the activities of the department (B2\-C1\). * GMP: knowledge of NCF/GMP or experience of working on a high regulated industry (recommended) * Organizational and planning skills: set goals and priorities when performing a task, agreeing on the action, deadlines, and resources to be used. * Strategic and improvement vision: encourage a culture of innovation and learning by contributing ideas and continuous improvements * Achivement of results: direct all actions towards the expected goal. * Excellent communication and interpersonal skills, with the ability to work collaboratively across teams. * Ability to work in a fast\-paced environment and manage multiple tasks effectively. * Company values: Humility, Empathy, Responsibility, Commitment, Teamwork, and Effort. **We Offer:** * A dynamic and collaborative work environment. * Opportunities for professional development and continuous training. * Direct impact on the development of therapies that improve people's lives. * Additional benefits; health insurance, vacation, flexibility, etc.