Radiopharmaceutical Lab Technician (Temporary

Job Description

Job DescriptionRadiopharmaceutical 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 potentially
• Vision 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.