Manufacturing Technician - Cold Products

Curium Pharma

Maryland Heights (MO)

On-site

USD 50,000 - 70,000

Full time

14 days+
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Job summary

Curium is hiring a Manufacturing Technician for Cold Products in Maryland Heights, MO. You will perform aseptically manufactured product tasks in an ISO 5 cleanroom following cGMP guidelines to meet production demands.

Position requires attention to detail, ability to follow complex procedures, and willingness to work rotating shifts, weekends, and overtime as needed. Safety and regulatory compliance are emphasized in daily responsibilities.

Qualifications

  • Knowledge of Good Manufacturing Practices (GMP) and applicable Quality System Standards.
  • Ability to follow detailed instructions and communicate effectively, both written and verbally.
  • Willingness to work rotating shifts, weekends, and overtime as necessary.

Responsibilities

  • Perform aseptically prepared product tasks in ISO 5 cleanroom per cGMP guidelines.
  • Set up, maintain, and clean production equipment and work area per SOP and cGMP.
  • Calibrate or adjust equipment to ensure quality production.
  • Troubleshoot equipment, devices, or products.
  • Collaborate with multiple departments to ensure production success.
  • Lift up to 70 pounds and perform required physical tasks as needed.

Skills

GMP knowledge
Attention to detail
Team collaboration
Effective communication

Education

High school diploma or equivalent
Associate degree preferred

Job description

Manufacturing Technician - Cold Products

Date: Aug 28, 2026

Location: Maryland Heights, MO, United States, 63043

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 preparing, formulating and dispensing aseptically manufactured products in and ISO 5 cleanroom environment according to cGMP Guidelines in order to meet production demands.

Schedule:
Monday through Thursday 0500-1530
Weekend and off shift overtime as needed

Essential Functions
  • Ensure a safe and quality working environment through training, awareness, and compliance to safety guidelines, SOP's and FDA regulations.
  • Responsible for following detailed instructions and communicating effectively, both written and verbally.
  • Perform Batch Record calculations and maintain all documentation according to cGMP Guidelines.
  • Set up, maintain, and clean appropriate equipment and work area according to SOP and in compliance with cGMP guidelines.
  • Set up, operate, and monitor production equipment and processes in accordance with current good manufacturing practices and standard operating procedures.
  • Calibrate or adjust equipment to ensure quality production, using internal calibration functions.
  • Participate and perform effectively in a team environment and interact with multiple departments to ensure the operational success of the team.
  • Responsibilities also include the ability to lift, reach, pull, and squat as needed, according to production demands.
  • Adhere to all applicable regulations, policies, and procedures for health, safety, and environmental compliance.
  • Troubleshoot problems with equipment, devices, or products.
  • 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
  • Associate Degree preferred, High school diploma or equivalent required.
  • 1 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.
  • Willingness to work rotating shifts, weekends, and overtime, as necessary.
  • Effectively adjusts to changes and deals effectively with uncertainties in the workplace.
  • Ability to generate new and valuable ideas and effective solutions to difficult problems; connects previously unrelated notions.
  • Realizing the worth of all people and respects others, regardless of background or cultural differences.
  • Thoroughly understanding the needs of internal/external customers and making customer satisfaction a top priority.
  • Strong motivation and ability to achieve work goals and quantifiable business results.
  • Ability and desire to cooperate, collaborate, and partner with others.
  • Willingness to help outside your department and within your department outside your normal or assigned responsibilities.
  • Has demonstrated the use of logical methods to solve problems with effective solutions and able to make quick quality decisions.
  • Dedicated to providing the highest quality product and meeting the expectations and requirements of internal and external customers.
  • Takes ownership and accountability for the production process, assigned production area, production equipment and associated documentation.
  • Good interpersonal skills and ability to communicate information in a timely manner to those who need the information.

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 anequal opportunity employerand believes everyone deserves respect, dignity and equality.All applicants will be considered for employmentwithout attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

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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