Pharmaceutical Manufacturing Technician - 2nd Shift
About The Position
SHINE Technologies is seeking a Pharmaceutical Manufacturing Technician to produce medical radioisotopes, supporting the company’s growth from clinical to commercial production. The role focuses on producing Lu-177 in cleanrooms using remote manipulators while meeting efficiency, quality, and safety standards. Work must comply with applicable federal, state, local, and company regulations, including cGMP requirements. The position follows a variable second-shift schedule: Monday 8:00 a.m.–6:00 p.m., Tuesday 10:00 a.m.–8:00 p.m., Wednesday 3:00 p.m.–3:00 a.m., and Thursday 1:00 p.m.–9:00 p.m.; Friday is off. Non-standard hours and shift work may occur periodically, rotationally, or on an ongoing basis. Overtime may sometimes be necessary with little or no advance notice, and some travel may be required. The base pay range is $25.00–$32.00 per hour, plus a comprehensive compensation package. Employment eligibility depends on qualifying for access to information subject to U.S. Export Controls. Eligibility may also depend on meeting Nuclear Regulatory Commission requirements for Safeguards Information access, typically including a pre-employment drug screen, fingerprinting, and criminal background check.
Requirements
- Ability to follow radiation safety and pharmaceutical requirements, including successfully passing all gown qualifications.
- Associate degree plus at least one year of experience, or high school diploma plus at least two years of experience in areas such as pharmaceutical or API manufacturing, equipment operation, or food processing.
- Strong mathematical skills, including algebra.
- Experience drafting documents such as SOPs and batch records.
- Willingness to learn and understand new technology, instrumentation, and technical processes.
- Ability to read engineering drawings or schematics.
- Ability to follow written procedures and accurately record test data.
- Ability to work safely in an industrial and radiation environment.
- Ability to qualify for access to information subject to U.S. Export Controls; eligibility may also be conditioned on meeting NRC Safeguards Information access requirements.
- Ability to work non-standard hours and shifts; overtime may sometimes be necessary with little or no advance notice.
- Some travel may be required.
Nice To Haves
- Experience working with radioactive materials and/or radioisotope production.
- Aseptic experience.
Responsibilities
- Maintain complete and accurate batch records and related documentation in accordance with cGMP/cGDP.
- Prepare materials and consumables for manufacturing Lutetium Chloride active pharmaceutical ingredient processes; perform cleaning, line clearances, and equipment system checks before aseptic processes.
- Perform production tasks, including receiving raw materials, processing radioisotopes in production hot cells, preparing sterile API, and shipping API to customers.
- Perform routine maintenance under the direction or supervision of a Manufacturing Engineer.
- Support the leadership team in identifying operational opportunities for continuous improvement and initiating process changes as needed.
- Maintain cleanliness of the work area and assist other work areas in maintaining a clean, professional environment.
- Use the Quality Management System to document maintenance, investigations, and change-control actions.
- Assist in writing deviations and investigations and initiating unscheduled work orders.
- Follow cGMP requirements at all times.
- Assist in training and developing other technicians.
- Assist other projects and departments and perform other duties as requested or assigned.
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What This Job Offers
Job Type
Full-time
Education Level
Associate degree
