Position Summary:Performing technical audit of GC/MS volatiles data in a timely manner with zero defects as a goal; acting as a technical resource to the department; evaluating issues in technical data and suggesting possible solutions; performing sample/QC verification in the LIMS; reviewing analytical reports, evaluating and interpreting analytical results; writing and revising SOPs; assisting in responding to and eliminating ICARs; making recommendations for technical improvements, communicating effectively within the department; completing assigned tasks on time; assisting in "brainstorming" client problems and projects; performing all duties with minimal supervision. Essential Duties and Responsibilities: Apply GMP/GLP in all areas of responsibility; as appropriate Demonstrate and promote the company visionRegular attendance and punctualityPerform technical audit of the dataReview corrections of dataAnalyze errors and provide feedback constructivelySuggest solutions to technical data issuesFollow flow of work through audit to verification Read, understand, and carry out SOPs required by EPA or company methods, governing agencies, clients, and our internal QC departmentUpload dataTroubleshoot basic upload issuesVerify data in LIMSReview analytical reportsUnderstand and use the LIMS, databases, and other software in a Windows-based environment Write/revise SOPs that conform to company and regulatory requirements Work on special projects as assigned, including ability to consult with clients on technical problemsConducts all activities in a safe and efficient mannerPerforms other duties as assigned This role is currently open on 2nd Shift, M-F 3pm-11:30pm. Training will be M-F 8am-4:30pm
- ID: #53962224
- State: Pennsylvania Lancaster 17601 Lancaster USA
- City: Lancaster
- Salary: USD TBD TBD
- Job type: Full-time
- Showed: 2025-06-04
- Deadline: 2025-08-03
- Category: Et cetera