QC Production Associate I
Not Disclosed•Full-TimeOn-site
location_onJohn M Collins Drive, Middlebush, Franklin Township, Somerset County, New Jersey, 08873, United States
About the Role
Join our team as a QC/Production Associate I, where you'll play a key role in producing life-changing drug products. In this position, you will ensure the highest quality standards through hands-on work with advanced radiosynthesizers and analytical equipment. You will operate synthesis units and QC instruments to produce FDG and NaF, while maintaining rigorous cGMP documentation and supporting a clean, safe working environment.
Our Mission
We are dedicated to advancing patient care through the precise production of radiopharmaceuticals. By adhering to strict corporate radiation compliance programs and site licensing requirements, we ensure that every product meets the highest standards of safety and efficacy for our patients.
Hiring Process
Interested candidates should submit their application with a resume highlighting their technical experience and ability to work in a fast-paced, highly technical environment. We look for individuals who are detail-oriented, accountable, and capable of working effectively in a team.
Equal Opportunity Employer
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
Work location
Work model: On-site
John M Collins Drive, Middlebush, Franklin Township, Somerset County, New Jersey, 08873, United States
Franklin Township, New Jersey
Key Responsibilities
- check_circleOperate radiosynthesizers to perform FDG and NaF synthesis according to SOPs
- check_circlePerform basic computer-controlled cyclotron operations under engineer advisement
- check_circlePerform radiation safety duties and maintain ISO classified area qualifications
- check_circleClean classified and non-classified areas and perform environmental monitoring
- check_circleConduct quality control processes for drug products using analytical equipment
- check_circleManage inventory levels for production, QC, and cleaning supplies
- check_circleMaintain production and QC equipment through routine maintenance and calibration
- check_circleEnsure completion of cGMP documentation including logs, investigations, and deviations
- check_circleReport manufacturing metrics into data repositories and assist with troubleshooting
Requirements
- verifiedHigh school diploma required
- verifiedAssociates degree in chemistry, engineering, or natural sciences preferred
- verifiedTechnical experience with computer-controlled automation preferred
- verifiedEfficient in the use of MS Office Suite required
- verifiedAbility to work various shifts and weekends required
- verifiedAbility to lift ~50 lbs. required
- verifiedUp to 5% travel required
Nice to Have
Associates degree in chemistry, engineering, or natural sciences. Technical experience with computer-controlled automation.
Similar Job Opportunities
Skills, education and keywords
Skills: Radiosynthesizers, Analytical Equipment, FDG, Naf, Sop, CGM P, MS Office Suite, Cyclotron, Iso Classified Area, Radiation Safety.
Education: High school diploma required; Associate's degree in chemistry, engineering, or natural sciences preferred.
Frequently asked questions about QC Production Associate I at SOFIE
What does a QC Production Associate I at SOFIE do?expand_more
In this QC Production Associate I at SOFIE role, you will operate radiosynthesizers to perform fdg and naf synthesis according to sops; perform basic computer-controlled cyclotron operations under engineer advisement; perform radiation safety duties and maintain iso classified area qualifications; and clean classified and non-classified areas and perform environmental monitoring.
What are the requirements for this QC Production Associate I role?expand_more
SOFIE is looking for candidates who meet the following requirements: High school diploma required; Associates degree in chemistry, engineering, or natural sciences preferred; Technical experience with computer-controlled automation preferred; Efficient in the use of MS Office Suite required; Ability to work various shifts and weekends required; and Ability to lift ~50 lbs. required.
Where is the QC Production Associate I role at SOFIE located?expand_more
QC Production Associate I at SOFIE is based in John M Collins Drive, Middlebush, Franklin Township, Somerset County, New Jersey, 08873, United States. This is a on-site role.
Is this QC Production Associate I job remote, hybrid, or on-site?expand_more
SOFIE has listed this QC Production Associate I role as on-site.
How much experience is required for this QC Production Associate I role?expand_more
Candidates for QC Production Associate I at SOFIE should have entry level.
What skills do you need for the QC Production Associate I role at SOFIE?expand_more
Key skills for QC Production Associate I at SOFIE include Radiosynthesizers; Analytical Equipment; FDG; Naf; Sop; CGM P; MS Office Suite; and Cyclotron.
What education is required for QC Production Associate I at SOFIE?expand_more
Educational requirements for this role: High school diploma required; and Associate's degree in chemistry, engineering, or natural sciences preferred.
What category does the QC Production Associate I role belong to?expand_more
QC Production Associate I at SOFIE is part of the manufacturing job category on Recrutus.