barycon inc

5 barycon inc job listings in United States. Find daily updated positions from leading job boards.


  • Clayton, NC, United States BaryCon INC. Full-time

    Job Description Job Description CQV / Validation Area Specialists - 6 Positions Reference: JQRI26SEP002 BaryCon is seeking six senior validation resources to lead CQV and validation activities across multiple pharmaceutical capital projects in Clayton, North Carolina. Assignments may cover facility systems, aseptic formulation and filling, device assembly...


  • Clayton, NC, United States BaryCon INC. Full-time

    Job DescriptionJob DescriptionCQV / Validation Area Specialists - 6 PositionsReference: JQRI26SEP002BaryCon is seeking six senior validation resources to lead CQV and validation activities across multiple pharmaceutical capital projects in Clayton, North Carolina. Assignments may cover facility systems, aseptic formulation and filling, device assembly and...


  • Clayton, NC, United States BaryCon INC. Full-time

    BaryCon leads CQV and validation activities across pharmaceutical capital projects in Clayton, North Carolina. Six senior validation resources are needed to cover facility systems, aseptic filling, device assembly, IT systems, warehouses, and QC facilities.Assignments are 100% onsite, 8:00 AM-5:00 PM, starting December 1, 2026, for 24 months with possible...


  • Clayton, NC, United States BaryCon INC. Full-time

    Job Description Job Description Validation Area Specialist - IT & Automation Reference: JQRI26SEP001 BaryCon is seeking a Validation Area Specialist to lead validation services supporting IT and automation projects at a pharmaceutical manufacturing site in Clayton, North Carolina. The role owns validation deliverables from planning through execution,...


  • Clayton, NC, United States BaryCon INC. Full-time

    BaryCon is seeking a Validation Area Specialist to lead validation activities for IT and automation at our pharmaceutical manufacturing site in Clayton, North Carolina. The role covers planning through execution, investigation, reporting, and transition to validated state, ensuring compliance with GMP and regulatory expectations.This is a full-time, 12-month...