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$75k–$90k/yr
Full-time
bachelor degree
401(k) retirement benefit program, Medical, Dental care, Disability insurance, Employee assistance program, Extended health care
Posted 22d ago
~40 hrs/week
Responsibilities
The Cyclotron Engineer is responsible for the routine maintenance, operation, and repair of PET site equipment, specifically focusing on cyclotron support. They ensure compliance with GMP and NRC regulations while documenting all engineering tasks and quality control activities.
Requirements
Candidates should have a bachelor's degree in science or a technical degree, with experience in PET or pharmaceutical manufacturing preferred. Strong analytical skills, mechanical aptitude, and the ability to work flexible hours including nights and weekends are required.
Hours: Hours may vary based on operational needs, including overnight shifts, weekends and being on call
Reports To: Regional Service & Engineering Manager
PharmaLogic is the fastest-growing SPECT & PET radiopharmaceutical solutions provider and contract development and manufacturing organization (CDMO) with radiopharmacies across North America. We are passionate about expanding the power of radiopharmaceutical technology to provide transformative diagnostic and therapeutic agents to patients from bench to bedside.
PharmaLogic offers you an exceptional opportunity to join our dynamic team as a Cyclotron Engineer!
Role Summary:
The Cyclotron Engineer will play an essential role in PET site operations through routine maintenance of the PET site's equipment with primary focus on cyclotron support.
Job Responsibilities and Duties:
Maintains a favorable working relationship with coworkers to promote a cooperative working climate conductive to maximum productivity, efficiency and effectiveness
Works with radioactive materials and follows all applicable procedures and regulations for maintaining ALARA practices
Ensures completion of required equipment, maintenance and calibration
Brings to Quality and operations manager's attention any product or component release problems and awaits management resolution if required
Documents, investigates and reviews any out of specification (OOS) or deviations as part of GMP compliance as it relates to engineering tasks
Coordinates with Facility Manager to schedule annual and additional preventive maintenance and associated production downtime
Follows good documentation practices all the time when documenting QA documents
Adheres to Company policies and procedures at all times
Liaises with Quality Manager to ensure any issues are addressed in a timely manner
Completes all planned Quality & Compliance training within the defined deadlines
Ensures safe work procedures and wears all required PPE Promptly reports all injuries and unsafe conditions
Supervises and/or assists in the operation and maintenance of the P.E.T. cyclotron
Supervises and/or assists in the preparation of P.E.T. isotopes and radiopharmaceuticals, including FOG
Maintenance of all required documents and records
During the Installation/ Commissioning phase of the equipment:
Participate in the installation of equipment
Technical responsibility over the Cyclotron subsystem
Participate in commissioning activities of the entire subsystem
During the Operations/ Maintenance phase:
Operation of the cyclotron according to proper operating procedures
Performs routine, non-routine, and emergency maintenance on the cyclotron
Maintains essential parts on site for cyclotron, manipulator arms and chemistry modules
Ensures completion of documentation related to cyclotron operations
Performs diagnosis and repair on the following: Electronic equipment, programmable logic controllers, power supplies, high voltage and high-power RF systems
Provides after-hours on-call support, requires working nights, weekends, and some holidays for maintenance and emergency support
Maintains and troubleshoot automated chemistry processing equipment
Designs and builds equipment to improve diagnostic and repair capabilities and implement reliability improvements for cyclotron and isotope manufacturing
Designs, develops and builds radioisotope production and chemical processing equipment
Assures compliance with all procedures, regulations, organizations, etc.
Participates in department technical training
Trend analysis and tracking of production systems performance data
Provides cyclotron operation coverage when required by the schedule
Perform routine, non-routine, and emergency maintenance of general laboratory equipment
Perform other job-related duties as assigned.
Job Requirements │ Skills │ Education:
Completion of manufacturer's applications training course for the cyclotron and chemistry modules.
Experience in PET manufacturing, pharmaceutical manufacturing (FDA and GMP regulated), nuclear pharmacy, chemistry training or comparable laboratory background preferred.
Bachelor's degree in science preferred or technical degree, electronics military training or equivalent experience.
Knowledge of cGMP and NRC regulations preferred
Strong interpersonal skills with an emphasis on effective communication and proven ability to interact effectively with stakeholders in a diverse population at all levels
Computer proficient, including knowledge of Microsoft Office (Word, Excel, Outlook)
Demonstrated organizational skills with the ability to manage time effectively in a fast-paced environment and a high volume of work
Analytical and problem-solving skills
Ability to accommodate shift changes based on business needs
Authorized user of radioactive material required
Knowledge of aseptic technique
Physical and Intellectual Requirements:
A mechanical aptitude; manual dexterity for manipulating small items; ability to lift between 16 to 50 lbs. and to handle frequent crawling, stooping, crouching and kneeling
Ability to analyze situations, set priorities and meet deadlines while maintaining attention to detail in a fast-paced and dynamic environment; effective organizational skills; a commitment to continuous learning
Ability to work well both independently and as part of a team
May require travel up to 25%
Come join our winning team and begin a fulfilling career with us by applying today. PharmaLogic is an Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status, or any other protected class.
Taking the lead in providing trusted quality and reliability in radiopharmaceutical manufacturing
Industry
Pharmaceutical Manufacturing
Company size
1,001-5,000 employees
Headquarters
Boca Raton, FL
LinkedIn followers
10,074
PharmaLogic is a leading global contract development and manufacturing organization (CDMO) specialized in diagnostic and therapeutic radiopharmaceuticals. With decades of industry expertise and a robust network of more than 45 facilities across the U.S., Puerto Rico, Canada, and Norway, PharmaLogic delivers comprehensive solutions spanning development, manufacturing, and distribution of both clinical and commercial-stage radiopharmaceutical products, all in accordance with the highest quality and regulatory standards. Our rapidly expanding diagnostics business leverages advanced technologies to enhance patient access to novel diagnostics in oncology, cardiology, and Alzheimer’s disease. In the therapeutic segment, PharmaLogic is the world’s only cGMP-compliant CDMO currently manufacturing and distributing a commercial radiopharmaceutical therapeutic across more than 30 countries. PharmaLogic is dedicated to enabling global patient access to radiopharmaceuticals through strategic development partnerships with industry innovators, advancing the future of the field and supporting our partners throughout the product lifecycle. For more information, visit radiopharmacy.com.
Offices: 5301 N Federal Highway, Boca Raton, FL 33487, US
Taking the lead in providing trusted quality and reliability in radiopharmaceutical manufacturing
Industry
Pharmaceutical Manufacturing
Company size
1,001-5,000 employees
Headquarters
Boca Raton, FL
LinkedIn followers
10,074
PharmaLogic is a leading global contract development and manufacturing organization (CDMO) specialized in diagnostic and therapeutic radiopharmaceuticals. With decades of industry expertise and a robust network of more than 45 facilities across the U.S., Puerto Rico, Canada, and Norway, PharmaLogic delivers comprehensive solutions spanning development, manufacturing, and distribution of both clinical and commercial-stage radiopharmaceutical products, all in accordance with the highest quality and regulatory standards. Our rapidly expanding diagnostics business leverages advanced technologies to enhance patient access to novel diagnostics in oncology, cardiology, and Alzheimer’s disease. In the therapeutic segment, PharmaLogic is the world’s only cGMP-compliant CDMO currently manufacturing and distributing a commercial radiopharmaceutical therapeutic across more than 30 countries. PharmaLogic is dedicated to enabling global patient access to radiopharmaceuticals through strategic development partnerships with industry innovators, advancing the future of the field and supporting our partners throughout the product lifecycle. For more information, visit radiopharmacy.com.
Offices: 5301 N Federal Highway, Boca Raton, FL 33487, US