Supplier Quality Engineer

Supplier Quality Engineer

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 Supplier Quality Engineer position is responsible for assisting with the Supplier Quality Program in compliance with applicable regulations. The position is responsible for supplier evaluations, Quality Agreements, corrective actions, vendor changes, metrics, filing and scanning documents. The position is also expected to participate in the internal auditing program and to support site regulatory inspections and customer audits, as applicable. This role is located at our Noblesville, IN facility.

Work Schedule: Monday – Friday 7:30 am – 4:00 pm, hours could be adjusted

Essential Functions:

• Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.).
• Conduct supplier evaluations, including assessments via questionnaire and audits, as applicable.
• Issue supplier complaints and drive for resolution and corrective action.
• Develop and maintain Supplier Quality Agreements
• Perform initial assessment of vendor changes, route for functional reviews, and track to completion.
• Participate in Internal Audits and assess subsequent corrective action recommendations.
• Provide support for FDA or other regulatory inspections and customer audits.
• Perform filing and scanning of documents.
• Execute and deliver on assigned project tasks in accordance with established timelines.
• Ensure a safe and quality working environment through training, awareness and compliance to regulatory guidelines and procedures.

Requirements:

• Bachelor of Science degree in Life Sciences or Engineering required, or equivalent experience.
• Three or more years of relevant experience in a pharmaceutical/medical device manufacturing environment with strong understanding of and exposure to applicable quality systems required.
• Working knowledge of cGMP guidelines and their application in a controlled aseptic environment preferred.
• Must have awareness of quality systems including Change Control, Internal Auditing, Corrective Action Program, Deviation and Complaint investigations, and Document Management.
• Must have experience with statistical tools.
• Proficient in use of Microsoft suite of products.
• Must possess strong problem solving, decision making, verbal and written communications skills.
• Must be results-oriented, able to make decisions, and prioritize work per business needs in a fast-paced environment.
• Must have ability to exercise independent judgment in planning, organizing, and performing tasks.
• Must have ability to communicate, motivate, and organize projects among a broad spectrum of personnel throughout the network, frequently under deadline pressure.
• Must be able to work with other groups to seek understanding and resolve issues, close gaps, and seek compliant outcomes.
• Must have ability to communicate with and positively influence broad and diverse populations within and outside the organization.

Working Conditions:

Willingness to work in plant producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels. Responsibilities include the ability to lift up to 70 pounds, kneeling, crouching, twisting the upper body, walking, bending, stooping, pushing, pulling, reaching, must be able to physically negotiate stairs and evacuation ladders with or without accommodation, wear and operate safety equipment, enter vessels, and inspect equipment. Material handling devices (e.g., hand truck, fork truck, and conveyors) are used when possible, however, use of proper lifting and movement techniques is necessary to prevent injury. Must be willing to wear a variety of Personal Protective Equipment (PPE) and hearing protection as needed. May be required to sit or stand for long periods of 8+ hours a day while performing duties. Must possess good hand-eye coordination; close attention to detail is required. Must be able to work indoors and outdoors with exposure to mechanical/moving parts, hazards including corrosive, flammable and toxic material, dust, dirt, odors, and irritants. Willingness to complete safety training within allotted timeframes, and work in a team-based environment. Must be able to work outside of regular work hours, including off shift, weekend, and holiday work as business needs require.

Disclaimer: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. 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.