Manufacturing Technician

Curium - Site de Saclay - CIS bio international; Maryland Heights (MO); On-site; Full time

Job summary

A leading company in nuclear medicine is seeking a Manufacturing Technician to join their team. This entry-level position involves assembling and packaging radioactive components while ensuring compliance with safety and quality standards. The role requires attention to detail and the ability to work in a team environment. The ideal candidate will have a high school diploma and some manufacturing experience. This position offers full-time hours with a work schedule from Saturday to Tuesday, 5:30 PM to 4:00 AM.

Qualifications

• One or more years of manufacturing experience required.
• Knowledge of Good Manufacturing Practices (cGMP) is essential.

Responsibilities

• Perform assembly, formulation, and packaging of radioactive components.
• Ensure compliance with safety guidelines and SOPs.
• Conduct room release checks for effective production.

Skills

Attention to Detail

Safety Awareness

Education

High School Diploma

College Coursework in Mechanics

Job description

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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.

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

Performs all tasks associated with assembling, formulating, dispensing, and packaging of radioactive components Reactor Hot Products (RHP) Lab according to cGMP guidelines in order to meet production demands. Participate in the manufacturing process within a team environment and interact with multiple departments to ensure the operational success of the facility. Train on aspects of the manufacturing process in the area(s) including but not limited to: overall process, individual task, trouble shooting, escalation plan, safety concerns, documentation, cleaning, cGMPs, SOPs, company policies, gowning and lean processes such as 5S and Kiazen.

Work Schedule: Saturday – Tuesday 5:30pm – 4:00am. Ability to overtime as needed.

Essential Functions

• Ensure a safe and quality working environment through training, awareness, and compliance to safety guidelines and SOP’s. Ensure the maintenance of their department, premises and equipment.
• Conduct room release to check for exceptions that would hinder effective production.
• Ensure proper maintenance and cleanliness of department (structure of area), premises (facilities) and equipment (all equipment and tools), report any deficiencies to coordinator and/or supervisor.
• Walk-through to check for irregularities that would hinder effective production.
• Perform line clearance to ensure nothing left from the previous lot and that the room is clean.
• Keep extensive log books to record important information in order to ensure compliance.
• Set up, maintain, operate and clean equipment and work area according SOPs and cGMP guidelines.
• Pick up and deliver raw materials from loading dock to production area using pallet jacks.
• Perform Batch Record calculations (including complex calculations) and maintain all documentation according to SOPs and cGMP Guidelines.
• Accurately label selected products with tracking and the appropriate FDA labels.
• Accurately count materials and labels to track used and unused raw materials for placement in the batch record.
• Demonstrate the ability to participate in the production processes with supervisor and/or leadership support. Monitor product quality to ensure compliance with standards and specifications.
• Ability to identify and verify appropriate materials, area conditions, process for production and elevate any abnormalities in the process, with materials or in area conditions to coordinator and/or supervisor.
• Assist and support (when appropriate), investigation, reliability team meeting, root cause analysis, SOP and Batch record improvements, Kaizen, Customer Complaints, data collection and downtime issue resolutions.
• Provide and maintain a safe work environment by participating in safety programs, committees, or teams and by conducting laboratory or plant safety audits.
• Prepare some chemical solutions for products or processes, following standardized formulas, or create experimental formulas.
• Order and inventory materials to maintain supplies.
• Participate and perform effectively in a team environment and interact with multiple departments to ensure the operational success of the team.
• Follow all written procedures and verbal instructions and communicate effectively, both written and verbally.
• Required to perform other duties that are not routinely part of direct responsibilities based on direction of manager’s / supervisor’s discretion to support overall business needs.
• Inspect finished products for quality and adherence to customer specifications.
• Start up and shut down processing equipment.
• 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.).
  
  

Requirements

• High school diploma or equivalent required. College level course work in Mechanics, Engineering Technical trade, or Chemistry preferred.
• One or more years of manufacturing experience required (regulated environment, attention to detail and following detailed instruction).
• Knowledge of Good Manufacturing Practices c(GMP) and applicable Quality System Standards.
• Must be willing to work around radioactive and/or non-radioactive materials.
  
  

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.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Management and Manufacturing

• Industries

  Pharmaceutical Manufacturing

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