What are the responsibilities and job description for the QC Program Coordinator Lvl I (CT) position at Lonza?
QC Program Coordinators represent the Quality Control department and act as a liaison between Quality Control and its internal and external customers. QC program coordinators are responsible for the management and execution of stability studies, as well as, being a QC representative within the lot release team.
Key Responsibilities:
- Document writing for transfers/validations/investigations
- Perform assay work for transfers/validations/investigations
- Responsible for the management and execution of stability studies
- Leads set up and verification of electronic equipment/templates/forms for transfers/validations
- Attending project team meetings
- QC Representative within the Lot Release Team
- Independently drive projects to on-time completion
- Other – such as leading OE initiatives, Improvements, hiring of staff
- Perform other duties as assigned.
Qualifications:
- BS/BA Science Or equivalent experience
- 2-4 Years of lab experience in biotech or medically related field
- Use of Microsoft Suites (Word, Excel, PowerPoint, Teams, SharePoint)
- Use of Laboratory computerized systems such as plate readers and chromatography platforms
- Use of GMP Quality Systems such as: TrackWise
- Very strong communication skills both written and verbal.
- Able to speak and convey messages and or information publicly.
- Makes quality decisions independently and also with guidance from Manager
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