Quality Engineering Manager

Schott North America
paid time off, long term disability, tuition reimbursement
United States, Pennsylvania, Lebanon
30 Lebanon Valley Parkway (Show on map)
May 14, 2025
About us Your Contribution Lead Quality Engineering and TCS departments Validate and re-revalidation of sterilization processes Manage the validation process Support experimental and validation protocols for equipment, processes and materials Manage the supplier quality management process Manage the process for customer driven changes and site transfers Manage the process for developing product specifications and quality attributes Support audits and prepare responses Coordinate Customer Quality Agreements Establish EM program Perform risk assessments Assign and/or manage CAPAs Your Profile Bachelor's Degree in Engineering, or related field, required Minimum (5) years of experience as a Quality Engineer Minimum (3) years of leadership experience in sterile product/process investigations, validations, instrument qualifications, customer support and EM Solid knowledge of ISO 9001, 14001, 15378, along with cGMP Experience in glass forming industry and/or pharmaceutical industry, preferred Sound computer knowledge and skills including MS Office, SAP and Minitab Multi-tasking abilities and prioritization Detail oriented approach; forward/creative thinking Positive team approach and ability to lead others Effective communication skills Ability to read, write and speak English language Your Benefits Excellent healthcare benefits including medical, dental and vision Short and long term disability Tuition reimbursement Paid time off Pet insurance Other supplemental benefits available upon election Please feel free to contact us Your Profile Bachelor's Degree in Engineering, or related field, required Minimum (5) years of experience as a Quality Engineer Minimum (3) years of leadership experience in sterile product/process investigations, validations, instrument qualifications, customer support and EM Solid knowledge of ISO 9001, 14001, 15378, along with cGMP Experience in glass forming industry and/or pharmaceutical industry, preferred Sound computer knowledge and skills including MS Office, SAP and Minitab Multi-tasking abilities and prioritization Detail oriented approach; forward/creative thinking Positive team approach and ability to lead others Effective communication skills Ability to read, write and speak English language Your Contribution Lead Quality Engineering and TCS departments Validate and re-revalidation of sterilization processes Manage the validation process Support experimental and validation protocols for equipment, processes and materials Manage the supplier quality management process Manage the process for customer driven changes and site transfers Manage the process for developing product specifications and quality attributes Support audits and prepare responses Coordinate Customer Quality Agreements Establish EM program Perform risk assessments Assign and/or manageCAPAs