Senior Quality Control Chemical Lab Analyst I bei PCCA

What We’re Looking For

The Senior QC Chemical Lab Analyst I is responsible for performing and reviewing a broad range of quality control tests to ensure that products meet established quality standards. This role involves day-to-day laboratory operations, ensuring full compliance with Standard Operating Procedures (SOPs), and maintaining accurate and complete documentation. The Senior Analyst I also plays a key role in investigating and resolving internal and external customer inquiries related to product quality. This position supports the continuous improvement of laboratory processes and may provide guidance and mentorship to other team members.

What You Will Do

• Create and revise Standard Operating Procedures (SOPs)

• Maintain an understanding of all Quality Control and Safety SOPs

• Document and review deviation reports 

• Review and disposition Quality Order Reports, new item set-up documentation and manufacturer item approval submissions 

• Provide guidance with the daily operations of QC laboratory

• Interpret Out of Specification results and guide analysts on investigative steps 

• Maintain knowledge of industry trends by attending trainings, reading journals, books and other appropriate literature

• Respond to all chemical spills (Code 7) 

• Ensure QC lab is compliant with 5S methodology for efficiency and effectiveness

• Communicate the status of unresolved quality issues and bring issues that require attention to management

• Train new QC team members 

• Assist with complaints directed to Quality Control; investigate, provide corrective action and issue reports of findings and trends

• Consult with vendors on relevant technical issues

• Assist QC analysts in regards to organization and prioritization of daily duties 

• Data entry and analysis, including interpretation

• Research and recommend new technology

• Record, troubleshoot and report equipment failure to QC Management 

• Assist with related special projects and other duties, as assigned

Who You Are

• Bachelor of Science Degree
• 3–5+ years of experience in a GMP-regulated quality control laboratory environment.
• Strong understanding of analytical techniques such as HPLC, FTIR, titration, and wet chemistry.
• Strong verbal and written communication skills
• Strong interpersonal, organizational and coaching skills
• Excellent attention to detail, organizational skills, and communication abilities.
• Understanding of Good Manufacturing Practices
• Ability to think analytically, solve problems and provide resolution to conflicts
• Ability to work in a collaborative team environment
• 2 years’ experience using Microsoft Word, Excel, Outlook, SharePoint, an ERP system(s) and chromatography data system