Our client is the world’s largest nuclear medicine company with more than a century of industry experience. They develop, manufacture and distribute world-class radiopharmaceutical products to help patients around the globe. Our client delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life-threatening diseases to over 14 million patients annually. Currently they are looking to expand the Indianapolis operation by adding a Sr QC Technician to their team.

　　Summary of Position:

　　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. May supervise the work of others and coordinate instrumentation use and completion of laboratory testing. Work under limited supervision with considerable latitude for the use of initiative and independent judgment.

　　Essential Functions:

　　Ensure a safe and quality working environment through training, awareness, and compliance to Safety/Quality guidelines and SOPs.

　　Analytical Method Validation and Verification (USP Compendial and Non-Compendial)

　　Analytical Equipment IOQ

　　Ensure the maintenance of the Analytical 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.

　　Top Skills:

　　Quality Control, Method Validation, Chemistry, Method Development, Analytical Testing

　　Must Haves:

　　Bachelor's or Master's Degree in Life Science

　　3+ years of analytical chemistry experience (HPLC, GC, or ICP most relevant)

　　2+ years of quality/lab experience within regulated industry or GMP facility (pharma preferred)

　　Added Plus:

　　Method development/validation experience

　　Relevant instrumentation experience with Analytical Balance, pH Meter, Automatic Pipettes, FTIR, UV-Vis, Voltammeter, Autotitrator, HPLC, GC, IC, ICP, Flame AA, TOC, Conductivity Meter.

　　Diversity, Equity & Inclusion

　　At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

　　Hiring diverse talent

　　Maintaining an inclusive environment through persistent self-reflection

　　Building a culture of care, engagement, and recognition with clear outcomes

　　Ensuring growth opportunities for our people

　　Actalent is an equal opportunity employer.

　　About Actalent

　　Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.