Share this Job

Process Engineer

Date:  Aug 6, 2022

Maryland Heights, MO, United States

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 Process Engineer – Active Pharmaceutical Ingredient (API) Hot Products provides technical discipline and leadership required to maintain, plan and implement robust and capable cyclotron derived API manufacturing processes, as well as upstream process activities at the Maryland Heights, MO facility.    This role will be responsible for performing the following: identifying and implementing improvements and new technologies to processes to increase productivity, improve quality and reduce costs; leading API process equipment troubleshooting efforts along with coordinating other support groups to return equipment to service; serving as a Subject Matter Expert (SME) and leading API product/process failure investigations, implementing corrective actions, and preparing sound scientific reports; authoring and providing technical support for developing new processes and equipment documents including URS (user requirements specifications), DOE’s (design of experiments), and validation documents; authors and/or reviews change control submissions to ensure the validated status of equipment is maintained; and reviewing, monitoring and trending operating data, consistently applying operational excellence and continuous improvement skills / tools in evaluating the data, and issuing related reports and recommendations for maintaining and improving process reliability.  Technical requirements will also include a thorough and demonstrable knowledge of cGMP's (Current Good Manufacturing Practice) and applicable industry standards.   The Process Engineer – API Hot Products will report directly to the API Hot Products Technical Manager and be responsible for working in collaboration with other manufacturing production, maintenance, and engineering team members, this role will also readily coordinate with members from the R&D, project engineering, quality assurance, quality control, validation, procurement, commercial sales and marketing, and distribution teams within Curium. 

Essential Functions

  • Leading process troubleshooting and remediation efforts.
  • Maintain control of API process changes including change control management and documentation.
  • Providing adequate and documented monitoring of the department API processes through trending, run reports, and tracking through SPC (Statistical Process Control) or other tools.  
  • Identify and support departmental change initiatives for continual process improvement, specifically around Operational Excellence, 6-Sigma and Lean Manufacturing applications.  Will serve as a departmental driver for cost reduction initiatives.
  • Assist in the development and maintenance of process equipment, procedures, batch records, and training materials.
  • Ability to influence proper operating procedures during the manufacture of API pharmaceuticals (Compliance with regulations, GMP behaviors / techniques, etc.)
  • Identifying capital needs for the department processes.
  • Support annual capacity analysis.
  • Facilitate technical transfers from R&D.
  • Provides technical expertise and support to project management teams during project lifecycles.
  • Executes low to medium complexity projects, including: 
    • Purchasing equipment to support API processes or manufacturing areas.
    • Composing associated capital request and processing financial information.
    • Capital funding for outside services as it relates to manufacturing (equipment upgrades, facility improvements, risk assessments, validation services, process engineering assistance).


  • Bachelor Degree in Chemical Engineering or related field required (other engineering disciplines may be considered based on professional experience.)
  • Three years or more of experience working as an engineer in an FDA regulated, GMP facility.
  • Three years or more of manufacturing experience; preferably in the manufacture of API and/or finished pharmaceuticals.
  • Experience in preferred in the following areas:
    • Ion-exchange chromatography
    • Electroplating
    • Small (volume), high value API production batches
  • Verifiable knowledge of and experience in application of cGMP's, validation, quality systems, document control and the impact of regulatory considerations on engineering initiatives.
  • Experience in applied knowledge of necessary behaviors and techniques associated with pharmaceutical production.
  • Knowledge of current industry practices and technologies
  • Proven experience in supporting and optimizing processes and equipment, as well as leading small teams, groups or efforts relating to those activities.
  • Experience applying formal Root Cause Analysis and problem-solving methodologies
  • Experience using SPC and other Operational Excellence methodologies; Lean and/or Six Sigma certification preferred
  • Experience with radioactive isotopes and radiation safety programs is preferred


Working Conditions:

  • Standard office environment, coupled with approximately 40% time in controlled radiopharmaceutical manufacturing environments.
  • Must be willing to wear a variety of personal protective equipment.  
  • Willingness to work in a plant producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels.
  • Responsibilities also include the ability to lift up to 70 lbs, walk, bend, stoop, push, pull, reach, and climb stairs with or without accommodation. 


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.


Job Segment: Process Engineer, Pharmaceutical, Document Control, QA, QC, Engineering, Science, Administrative, Quality