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Senior Manufacturing Technician

Job in Maryland Heights, St. Louis city, Missouri, 63043, USA
Listing for: Curium Pharma
Full Time position
Listed on 2026-01-24
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Quality Engineering
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Location: Maryland Heights

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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

The role of a Senior Manufacturing Technician is to perform all tasks associated with operating equipment through formulation, preparation, dispensing and packaging of aseptically filled radiopharmaceutical processes, according to cGMP guidelines to meet production demands. The Senior Manufacturing Technician will work with advanced automated equipment, in the creation of new products, and serve as one of several technicians while coordinating work in accordance with standard operating procedures (SOP’s).

Schedule:

Saturday - Tuesday 5pm - 3:30am. Ability to work overtime when necessary

Essential Functions
  • Ensure a safe and quality working environment through training, awareness, and compliance to safety guidelines, SOP’s as well as US and international regulations (i.e. FDA, HC, EU, TGA, etc.).
  • Perform and document tasks associated with the production of radiopharmaceuticals in accordance with Federal and/or State guidelines in a cGMP environment.
  • Participate and perform effectively in a team environment and interact with multiple departments to ensure the operational success of the area.
  • This position will coordinate with Staging, Warehouse, Label Control, and Production Supervisors to plan, schedule, and execute all aspects of the area.
  • Monitor and inspect product quality to ensure compliance with standards and specifications.
  • Must pass Visual Acuity, Color Vision Test and Respiratory Test as required for process needs.
  • Adhere to all applicable regulations, policies, and procedures for health, safety, and environmental compliance.
  • Perform Batch Record calculations, reviews and maintain all documentation according to cGMP Guidelines.
  • Follow detailed instructions and communicate effectively, both written and verbally.
  • Set up, operate, monitor, and clean production equipment and processes in accordance with current good manufacturing practices and standard operating procedures.
  • Ensures the maintenance and cleanliness of department, premises, and equipment.
  • Order and maintain inventory of materials and supplies.
  • Act as demonstrators and/or qualifiers for processes and procedures during the training of new employees.
  • 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.).
  • Works with leadership to improve operations.
  • Must be willing to attend additional training when required.
  • Demonstrates willingness to be flexible to the needs of the department and business, including outside of the department.
  • Takes ownership and is an active member with continuous improvement activities including: reliability team meetings, root cause analysis, SOP and Batch record improvements, Kaizen events, and Customer Complaints.
Requirements
  • High School Diploma or equivalent required.
  • Three or more years of relevant work experience is required, preferably in a pharmaceutical or manufacturing industry.
  • Proven high performer capable of meeting or exceeding goals on time as well as meeting objectives…
Position Requirements
10+ Years work experience
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