QC Analyst III
PharmaMedTechRegulatory AffairsQuality Assurancegmpcroinform
Job description
Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives. Experienced QC Analyst – Bioanalysis Labcorp is seeking an onsite Experienced QC Analyst to join our new CMC facility in Mechelen, Belgium. Job Responsibilities: Perform and oversee analytical testing in accordance with GMP requirements, study protocols, and laboratory procedures. Review and evaluate test results, investigate trends or deviations, and support problem resolution activities. Collaborate with QC Scientists and cross-functional teams to ensure studies are delivered on time and to the highest quality standards. Receive and register samples, ensure the lab is clean at all time Support method troubleshooting, transfer, validation, and continuous improvement initiatives. Maintain laboratory equipment, documentation, and quality records in line with regulatory requirements. Ensure compliance with data integrity standards and GMP regulations. Contribute to audits, inspections, investigations, and quality improvement activities. Serve as a subject matter expert for analytical techniques and support the successful execution of complex projects. Minimum Qualifications: Bachelor in Science 5 years or more experience of analysis in the pharmaceutical industry or a regulated laboratory 4 or more years experience with PCR, bioassay and chemical testing (compendial, CE, HPLC) Preferred Qualifications: 2 or more years experience with GMP in a QC environment Additional Job Standards: Proficient in English, Dutch is an added value Computing skills, including word processing and use of spreadsheets (e.g. Microsoft Office packages). Skilled in independently performing a wide variety of analytical techniques. An understanding of health and safety policies, Company policies and procedures. Excellent communication skills (written and spoken) Can-do mentality Flexibility to perform other lab related tasks when needed In this role, you will work closely with QC Scientists and project teams to deliver high-quality analytical results while ensuring compliance with GMP and regulatory standards. They are responsible for the efficient and effective completion of analysis, maintenance of study documentation, and laboratory records. They are responsible for ensuring that all work is completed in accordance with the laboratory schedule, all relevant SOPs or policies and according to scientific and technical standards, including GMP. The QC Analyst will carry out operational activities necessary for the performance of a wide variety of studies carried out in the department and will maintain a clean and safe laboratory work environment. Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement .
Stand out for this role
NoxPharm tailors your CV to this job description by aligning your experience with the role requirements and terminology. Built for pharma & life sciences.
Tailor my CV now — free to trySimilar Pharma jobs
Business Data Analyst - Lab process reengineering.
Eurofins — Murcia, es
Business Intelligence Analyst
Eurofins — Nantes, fr
Wissenschaftler/ Chemieingenieur / Chemielaborant mit GMP (m/w/d)
Eurofins — Planegg, de
Chargé(e) de stratégie
Eurofins — Dijon, fr
Stage Customer Service
Eurofins — Vimodrone, it
Customer Service Internship
Eurofins — Madrid, es