Quality Control Manager

Social network you want to login/join with: Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas . Due to our constant growth, we are looking for a Quality Control Manager to join a project for one of our most important client based in Anagni . Key Responsibilities: Lead, organize, and supervise daily activities in the QC laboratory to ensure efficient, compliant, and high-quality operations. Manage the planning, implementation, review, and continuous improvement of lab processes and workflows. Coordinate and support analytical method transfers and validations for biotechnological products, especially peptides and recombinant proteins . Provide technical guidance and oversight to QC Analysts, Supervisors , and Assistants , ensuring accurate execution of test methods and adherence to GMP standards. Collaborate with R&D, QA, and Manufacturing to support cross-functional projects and drive process alignment. Prepare and review SOPs, protocols, CAPAs, deviations , and method transfer documentation in line with regulatory expectations. Conduct root cause analyses and support investigations using systems such as TrackWise . Optimize resource allocation, manage laboratory scheduling, and support the career development of junior staff. Assist in the selection, training, and mentoring of a future QC Supervisor from the client’s internal team. Promote a culture of ownership, compliance, and teamwork within the QC department. About You: 5–6 years of experience in Quality Control or Analytical Development within the pharmaceutical or biotech industry. Minimum 2 years of experience in a supervisory or team leadership role (e.g., QC Manager, QC Supervisor, Assistant QC Manager). Hands-on experience with techniques such as HPLC/UPLC, GC, LC-MS, UV-VIS, IR spectroscopy, KF titration, SDS-PAGE , etc. Strong knowledge of method validation and transfer , especially under GMP and ICH guidelines. Proficiency in lab software such as Empower 3, LIMS, TrackWise , and scientific instruments Skilled in team planning, performance monitoring , and lab process optimization . Familiarity with Change Control, CAPA, deviation management , and data integrity best practices. Excellent organizational, documentation, and communication skills. Experience in project tracking (e.g., Gantt charts), reporting, and technical problem solving. Location : Anagni (Italy) 100% onsite Available to travel in Italy and Europe Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us. J-18808-Ljbffr

Location: provincia-di-modena, IT

Posted Date: 6/7/2025