Pharmaceutical Manufacturing Technician - 3rd Shift at SHINE Technologies LLC

Janesville, Wisconsin, United States -

Full Time

Start Date

Immediate

Expiry Date

19 Jun, 26

Salary

35.0

Posted On

21 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

cGMP, cGDP, Aseptic Processes, Radioisotope Production, Batch Records, SOP Drafting, Radiation Safety, Quality Management System, Deviation Investigation, Change Control, Equipment Operation, Material Preparation, Sterile API Preparation, Mathematical Skills, Engineering Drawings

Industry

Energy Technology

Description

Description SHINE Technologies is immediately seeking a 3rd Shift Pharmaceutical Manufacturing Technician to perform production of medical radioisotopes and play a major part in growing our manufacturing operations as we start with clinical production and move into commercial production. These positions will perform operations with focus on efficiency, quality and safety standards while using remote manipulators in cleanrooms to produce Lu-177. Shift: Monday - 6:00am 10:00am & Tuesday - Thursday 8:00pm - 8:00am $3.00/hour 3rd Shift Premium The base salary range for this position is $20/hour-$35/hour plus a comprehensive compensation package. Our salary ranges are determined by role, level, and location. Duties and Responsibilities: All below listed responsibilities must be completed in compliance with federal, state, local, and company-specific regulations related to quality of product, employee and customer safety, and to the proper performance of day to day operations. The essential functions of this position include, but are not limited to: Maintain complete and accurate batch records and related documentation in accordance with cGMP/cGDP. Prepare materials/consumables for the manufacturing processes of active pharmaceutical ingredient Lutetium Chloride and perform cleaning activities, line clearances, and system checks on equipment before use in aseptic processes. Perform production tasks such as receiving raw materials, processing radioisotopes in production hot cells, preparing the sterile API and shipping the API to our customers. Perform routine maintenance under direction or supervision of Manufacturing Engineer. Support leadership team in identifying operational opportunities for continuous improvement, initiating changes to processes as needed. Maintain general cleanliness of work area and assist other work areas as needed to ensure a clean and professional environment. Utilize Quality Management System to document maintenance, investigations and change control actions. Assist in writing deviations, investigations and initiate unscheduled work orders. Strict adherence to cGMP at all times. Assist in training and development of other technicians. Assist other projects and departments and perform other duties as requested or assigned. Requirements Ability to follow and observe all radiation safety and pharmaceutical requirements, including successfully passing all gown qualifications. Associate degree plus a minimum of one year experience or high school diploma with 2 or more years of experience in areas such as pharmaceutical or API manufacturing, equipment operator, and food processing. Strong mathematical skills including algebra. Experience drafting documents such as SOPs and batch records required Experience working with radioactive materials and/or radioisotope production is a plus. Aseptic experience preferred Willingness to learn and understand new technology, instrumentation and technical processes. Ability to read from engineering drawings or schematics. Ability to follow written procedures and accurately record test data. Ability to work safely within an industrial and radiation environment. The position will require non-standard work hours and shift work, on a periodic, rotational or ongoing basis. Overtime may sometimes be necessary to complete required work assignment with little or no advance notice. Some travel may be required. Eligibility for employment is conditioned on the applicant’s ability to qualify for access to information subject to U.S. Export Controls. Additionally, applicant’s eligibility may be conditioned based upon meeting the Nuclear Regulatory Commission requirements for access to Safeguards Information, which typically requires a pre-employment drug screen, fingerprinting and criminal background check. SHINE values diversity in all its forms as a critical component of innovation, which is fundamental to our success. Every member of the SHINE community benefits from the talents and experiences of our peers, from the mutual respect we exercise, and from the responsibility we take for our actions. SHINE Technologies 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. Pay Transparency Policy Employee Rights Under the NLRA Equal Opportunity Employment E-Verify

Responsibilities

The technician will perform the production of medical radioisotopes, specifically Lu-177, focusing on efficiency, quality, and safety standards while operating in cleanrooms using remote manipulators. Key duties include maintaining accurate batch records, preparing materials, processing radioisotopes in hot cells, and shipping the final Active Pharmaceutical Ingredient (API).