
QC Analyst
- Waterford
- Contract
- Full-time
- Isolate particles from sterile biologics and contribute to investigations into their origin.
- Perform analytical techniques such as FTIR, Scanning Electron Microscopy, and RAMAN Spectroscopy.
- Provide analytical chemistry services and support across the site.
- Collaborate effectively with departments like Quality Assurance, Production, Engineering, and Planning.
- Maintain and update chemical methods, specifications, and SOPs in compliance with regulatory standards.
- Train analysts in new methods, SOPs, and areas of expertise.
- Trend results, record data on Certificates of Analysis (COAs), and complete Out-of-Specification (OOS) investigations promptly.
- Communicate potential issues and suggest improvements to the QC Team Leader.
- Ensure all quality documentation and records are accurate and up-to-date.
- Maintain compliance with current Good Laboratory Practice (cGLP) and Good Manufacturing Practice (cGMP).
- Validate critical testing equipment and ensure it meets IQ, OQ, and PQ requirements.
- Audit and review test results, laboratory notebooks, and analytical reports for accuracy and compliance.
- Proficiency in analytical techniques such as FTIR, Scanning Electron Microscopy, and RAMAN Spectroscopy.
- Strong understanding of cGLP and cGMP requirements.
- Experience in maintaining and updating SOPs and chemical methods.
- Ability to collaborate across departments and communicate effectively.
- Skilled in conducting investigations and trend analysis.
- Attention to detail in auditing and reviewing laboratory documentation.
- Familiarity with validation processes for testing equipment.
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