North Carolina All, NC
Demonstrates an understanding of technical concepts supporting methodology and systems in Material or Product Testing.
Performs troubleshooting and initial investigative work related to OOS, OOT.
Leads others consistently in productivity, quality and teamwork metrics. Drives continuous improvement initiatives within Quality Control.
Demonstrates independence and proficiency in performing tests for most products supported by work group.
Works with supervisors to plan and complete testing, data evaluation and LIMS reporting. Meets productivity, quality and teamwork metrics for level.
Is responsible for other duties such as report writing, advanced studies and investigational research within the QC organization as determined by management.
Maintains proper documentation of laboratory data (which requires adequate proficiency in written and computational skills).
Conducts all testing in compliance with cGMP and SOP s.
Will lead and assist in the training of others within workgroup.
- Support in investigations when needed.
This role may support pharmaceutical solid oral dosage finished drug product or pharmaceutical raw materials testing Group. Candidates preferably have experience executing in a solid oral dosage pharmaceutical environment.
Must have strong GMP and quality mindset and the willingness to support business needs. Must be open to working OT and weekends if necessary.
BS or MS in Chemistry or Life Sciences.