Quality Engineering Manager Position Available In Lebanon, Pennsylvania
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Job Description
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) Jun 11, 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