New

Quality Assurance Specialist

Schott North America
paid time off, long term disability, tuition reimbursement
United States, Pennsylvania, Lebanon
30 Lebanon Valley Parkway (Show on map)
Jul 10, 2025
About us Your Contribution Assist in reviewing customer reinspection paperwork for returned product Write and/or update Standard Operating Procedures (SOPs) and forms pertaining to job scope and functions Prepare and approve job totes Review completed batch manufacturing records to ensure cGMP, record thoroughness and adherence to internal and external customer specifications Generate Certificates of Conformance/Analysis according to customer requirements and specifications Maintain and update applicable quality document files; such as, CoC and CoA templates, paperwork hold report(s), pallet hold report(s), etc. Assist with customer complaint investigations as needed, to include but not limited to, measuring, batch record review, sending samples to SCHOTT Pharmaceutical Services, etc. Work on special projects, as assigned Participate in required trainings and meetings, when necessary Follow all Company policies and procedures Cross train in other Quality areas and/or functions to support business needs Help promote and implement safety/EHS directives and maintain a clean and safe workspace Follow cGMP and adhere to all ISO and safety guidelines, policies and protocols Your Profile High School Diploma or GED, required Minimum 2 years of experience in a Quality related manufacturing role, preferred Experience working in a fast-paced manufacturing setting Understanding of cGMP and ISO, preferred Basic computer knowledge and skills including MS Office and SAP Multi-tasking abilities Detail oriented approach; ability to follow directions and instructions Positive team approach 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 You can expect interesting tasks and challenging projects, as well as motivated and friendly teams in fields that influence our future. Do you want to be successful with us? Then, please send us your application: SCHOTT Pharma USA Inc, Human Resources, Kurt Johnson, +17172284231 *At SCHOTT, it's your personality that counts - not your gender, your identity, or origin. Your Profile High School Diploma or GED, required Minimum 2 years of experience in a Quality related manufacturing role, preferred Experience working in a fast-paced manufacturing setting Understanding of cGMP and ISO, preferred Basic computer knowledge and skills including MS Office and SAP Multi-tasking abilities Detail oriented approach; ability to follow directions and instructions Positive team approach Effective communication skills Ability to read, write and speak English language Your Contribution Assist in reviewing customer reinspection paperwork for returned product Write and/or update Standard Operating Procedures (SOPs) and forms pertaining to job scope and functions Prepare and approve job totes Review completed batch manufacturing records to ensure cGMP, record thoroughness and adherence to internal and external customer specifications Generate Certificates of Conformance/Analysis according to customer requirements and specifications Maintain and update applicable quality document files; such as, CoC and CoA templates, paperwork hold report(s), pallet hold report(s), etc. Assist with customer complaint investigations as needed, to include but not limited to, measuring, batch record review, sending samples to SCHOTT Pharmaceutical Services, etc. Work on special projects, as assigned Participate in required trainings and meetings, when necessary Follow all Company policies and procedures Cross train in other Quality areas and/or functions to support business needs Help promote and implement safety/EHS directives and maintain a clean and safe workspace Follow cGMP and adhere to all ISO and safety guidelines, policies and protocols