Quality Control Specialist / Junior Specialist
Kocaeli, Türkiye
About Curium
Curium is the world’s largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world-class radiopharmaceutical products to help patients around the globe. Our proven heritage combined with a pioneering approach are the hallmarks to deliver innovation, excellence and unparalleled service. With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life-threatening diseases to over 14 million patients annually. The name ‘Curium’ honors the legacy of pioneering radioactive researchers Marie and Pierre Curie, after whom the radioactive element curium was named and emphasizes our focus on nuclear medicine. The tagline ‘Life Forward’ represents our commitment to securing a brighter future for all those we serve: An enhanced quality of care for our patients. A trusted partner to our customers. A supportive employer to our valued team.
Summary of Position
The Quality Control Specialist is responsible for ensuring laboratory operations comply with GMP, GLP, and GRP standards, performing analytical testing, managing equipment calibration and validation processes, and overseeing method development and stability studies to ensure product quality and regulatory compliance.
Essential Functions
- Ensure that Quality Control Laboratories operate in compliance with GMP, GLP, and GRP requirements; manage and oversee laboratory activities effectively and efficiently.
- Perform and ensure all required testing for raw materials, packaging materials, in-process, and finished products in accordance with GRP, GLP, GMP, and approved documentation.
- Plan and ensure the execution of calibration and/or validation/qualification programs for laboratory equipment.
- Prepare or ensure the preparation of procedures and instructions related to Quality Control Laboratory activities; keep procedures and records up to date.
- Develop new analytical methods and perform or ensure method validation.
- Conduct and ensure stability studies in accordance with relevant guidelines and procedures.
- Comply with shift schedules and fulfill shift responsibilities according to the analysis plan.
Requirements
- Bachelor’s degree in Chemistry or Chemical Engineering.
- Preferably at least 3 years of experience in pharmaceutical manufacturing, with hands-on experience in GC, HPLC, TLC, and preferably ICP-MS instruments.
- Excellent command of English.
- Proficiency in Microsoft Office applications.
- Preferably knowledge of SAP and QMex systems.
- Residing in or able to reside in Istanbul (Anatolian side) or Kocaeli (Gebze).
Equal Opportunity Employer
Curium is an equal opportunity employer and believes everyone deserves respect, dignity and equality. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
We believe diversity includes disability, and we actively encourage applications from people with disabilities. If you require any accommodations during the recruitment process, please let us know—we are happy to support you.
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Chemical Research, QC, Medical Technologist, Nuclear Engineering, Compliance, Engineering, Quality, Healthcare, Legal
