Job Description
Job Description
Radiopharmaceutical Lab Technician (Temporary Contract)
Department : CMO Production
Reports To : Manager, CMO Operations
Location : On-site in Wilmington, MA
Position Summary :
We are seeking a hands-on Radiopharmaceutical Lab Technician to support GMP manufacturing and laboratory operations. This temporary contract role plays a key part in ensuring a clean, organized, and compliant production environment, while assisting in daily manufacturing activities. The ideal candidate is safety-focused, detail-oriented, and comfortable working early shifts in a regulated setting.
Key Responsibilities :
- Support daily production activities under the supervision of the Manager of CMO Operations.
- Assist with physical and electronic inventory tracking of production materials.
- Maintain cleanliness and perform routine maintenance of cleanroom facilities and production equipment.
- Assist in the handling and documentation of radioactive waste management activities.
- Assist with technical transfer related tasks and documentation.
- Participate in documentation activities, including authoring and revising SOPs.
- Support deviation investigations, root cause analysis, CAPA implementation, and non-conformance tracking.
- Operate and maintain production and laboratory equipment in accordance with established protocols.
- Perform additional duties as assigned by the Manager of CMO Operations.
Required Qualifications :
Associate degree or equivalent; scientific coursework required. Bachelor’s degree in a life science or related field preferred.Proficiency in Microsoft Office Suite (Word, Excel, Outlook).Ability to read, understand, and follow detailed written and verbal instructions.Able to lift up to 50 lbs and stand for extended periods in a cleanroom environment.Must have flexibility for working days at times with early morning start and potentiallyVision correctable to 20 / 20.Fluent in written and spoken English.Preferred Skills & Experience :
Prior experience in a GMP-regulated manufacturing or laboratory environment.Willing to learn and be trained on routine production activities.Active involvement of technical transfers as assigned by the by the Manager of CMO Operations, including authoring and revising SOPs.Self-starter with the ability to work independently and collaboratively in a fast-paced setting.Strong attention to detail, organization, and safety compliance.