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 (Contractor) Quality Control Testing Engineer role is responsible for performing analytical testing of raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with regulatory and company standards. This role is critical to maintaining product quality, supporting production timelines, and ensuring regulatory compliance.
Work schedule: Monday – Friday 8am – 4:30pm

REQUIREMENTS

• Bachelor of Science in Biology, Chemistry or related field required.
• 2 or more years of relevant experience required.
• Solid knowledge of analytical techniques and instrumentation (HPLC, GC, etc.).
• Familiarity with cGMP, GLP, and regulatory guidelines.
• Must be able to resolve problems, handle conflict and make effective decisions under pressure, and conduct Root Cause Analysis.
• Ability to do simple to complex math calculations, input data into the computer and analyze data as required.
• Ability to multitask projects.
• Must be proficient in use of Microsoft suite office products.
• Good computer skills, including utilizing personal computers and data entry programs Good hands on, analytical, and problem solving and decision making skills.
• Excellent writing and verbal communications skills.
• Ability to work independently and with others to accomplish goals and priorities High level of energy and regular, consistent attendance.
• Verifiable working knowledge of cGMP guidelines and their application in a pharmaceutical manufacturing environment.

• Perform routine and non-routine analytical testing using techniques such as HPLC, GC, UV-Vis, FTIR, titration, ICP-MS etc.
• Conduct testing on raw materials, intermediates, and finished products in accordance with cGMP and SOPs.
• Review and interpret analytical data; prepare detailed and accurate reports and documentation.
• Maintain laboratory equipment, including calibration, qualification, and troubleshooting.
• Participate in method development, method validation, and stability studies as required.
• Ensure compliance with all applicable regulatory requirements (e.g., FDA, EMA, ICH) and internal quality standards.
• Support investigations (OOS, OOT, deviations) and assist in root cause analysis and CAPA implementation.
• Maintain a clean and organized laboratory environment and adhere to safety guidelines.
• Participate in audits and inspections and support documentation requests from regulatory authorities.