Perform assigned laboratory testing and related quality control activities in order to ensure compliance with applicable SOP's and cGMPs. Provide timely testing and notification of any aberrant occurrence to Management/Supervision that presents potential negative impact to manufactured or marketed product. This is an overnight position working directly with radioactive materials.

Schedule:

Saturday - Tuesday 7pm - 5:30am

• Ensure a safe and quality working environment through training, awareness, and compliance to Safety/Quality guidelines and SOPs.
• Ensure the maintenance of their department, premises, and equipment.
• Ensure that all necessary training is carried out to perform all the assigned tasks confidently and consistently.
• Perform all work in compliance with site safety and radiation protection guidelines.
• Collaborate with other team members to ensure that quality tasks are performed in a timely manner.
• Must demonstrate flexibility in adjusting to changing priorities and schedules.
• Attend mandatory trainings as required by site regulatory requirements and management.
• Assist with investigations by providing testing results and communication of practice(s).
• Perform other general duties associated with the position as required by supervision.

• AssociateDegree in life science or a related field or completion of four college-level life science courses required. Bachelor Degree in life science or a related field preferred.
• 1 or more years of relevant quality / quality control / production experience in a cGMP facility required
• General quality / quality control / production experience in a cGMP facility required.
• Proficient in the use of several of the following laboratory instruments: Analytical Balance, pH meter, automatic pipettes, FTIR, UV-Vis, Voltammeter, Autotitrator, HPLC, GC, IC, ICP, Flame AA, TOC, Conductivity meter.
• Ability to work independently and with others to accomplish goals and priorities.
• Flexibility and teamwork skills.
• High level of energy and regular, consistent attendance.

Working Conditions:

• Willingness to work in a plant producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels.
• Standard office environment, coupled with approximately 80% time in radiopharmaceutical manufacturing and laboratory environments.
• Must be willing to wear a variety of personal protective equipment.
• Willingness to work in a team-based environment.
• Close attention to detail required.
• May be required to sit or stand for long periods of time while performing duties.
• Must be able to work outside of regular work hours.
• Responsibilities also include the ability to lift up to 70lbs, walk, bend, stoop, push, pull, reach, and climb stairs with or without accommodation.
• Must possess good hand-eye coordination.