Role: Associate I, Quality Control Lab Chemistry
Performs routine and nonroutine analytical testing of raw materials, inprocess samples, intermediates, and finished goods to support material release for production use. This role ensures testing activities are executed in accordance with approved SOPs, quality standards, and regulatory requirements while supporting production and project timelines. The associate is responsible for completing accurate and compliant documentation related to analytical testing and product inspection, and for entering data into electronic systems such as SAP and LIMS. Results and material disposition are communicated clearly and timely to internal and external stakeholders.
This role ensures inspections and testing activities are completed in alignment with SOPs, quality expectations, and the production plan. The associate communicates defects, atypical results, and quality concerns to laboratory supervision and Quality Assurance to support investigations and corrective actions. The Associate I maintains strict adherence to data integrity practices, including ALCOA+ principles, and is responsible for reviewing and verifying test data for accuracy, completeness, and compliance. Timely reporting of results is critical to support product release, project deliverables, and business needs.
The role also participates in daytoday laboratory operations, including safety, quality initiatives, 5S activities, and required training. The associate supports continuous improvement projects within a defined scope and demonstrates compliance with ISO, FDA, and GMP requirements. A strong commitment to promoting a culture of quality, safety, and compliance is essential.
Experience:
Need experience working in a regulated Quality Control lab using GC, HPLC, pH, titrator, particle size analyzer
Required Skills:
GMP Practice: Understanding of GMP laboratory operations. Ability to follow detailed procedures and work independently.
Analytical Skills: Need strong analytical abilities to identify and troubleshoot quality issues. They should be able to interpret and analyze data.
Problem-Solving Skills: Basic troubleshooting and problemsolving abilities.
Communication Skills: Strong communication and teamwork skills. They need to communicate effectively with team members, management, and external vendors to ensure everyone is aligned on quality standards.
Attention to Detail: Strong attention to detail for identifying potential quality issues and documentation accuracy.
Time Management: Effective time management and prioritization skills.
Preferred: Experience with LabVantage or similar LIMS, Empower 3, or similar data acquisition systems.
Bachelors Degree in Chemistry
Custom Fields:
Name: System Access Required
Value: Yes
Name: Badge ID Required
Value: Yes
Name: Supervisory Org
Value: QC Labs H(Ahmad Weeks)-60002819
Name: Invoice Type
Value: USA-ARL-Staffing-USD
Name: Workspace
Value: None
Name: Worker Time Type
Value: Full Time
Name: Work Desk Phone Number Required
Value: No
Name: Remote Worker
Value: No
Performs routine and nonroutine analytical testing of raw materials, inprocess samples, intermediates, and finished goods to support material release for production use. This role ensures testing activities are executed in accordance with approved SOPs, quality standards, and regulatory requirements while supporting production and project timelines. The associate is responsible for completing accurate and compliant documentation related to analytical testing and product inspection, and for entering data into electronic systems such as SAP and LIMS. Results and material disposition are communicated clearly and timely to internal and external stakeholders.
This role ensures inspections and testing activities are completed in alignment with SOPs, quality expectations, and the production plan. The associate communicates defects, atypical results, and quality concerns to laboratory supervision and Quality Assurance to support investigations and corrective actions. The Associate I maintains strict adherence to data integrity practices, including ALCOA+ principles, and is responsible for reviewing and verifying test data for accuracy, completeness, and compliance. Timely reporting of results is critical to support product release, project deliverables, and business needs.
The role also participates in daytoday laboratory operations, including safety, quality initiatives, 5S activities, and required training. The associate supports continuous improvement projects within a defined scope and demonstrates compliance with ISO, FDA, and GMP requirements. A strong commitment to promoting a culture of quality, safety, and compliance is essential.
Experience:
Need experience working in a regulated Quality Control lab using GC, HPLC, pH, titrator, particle size analyzer
Required Skills:
GMP Practice: Understanding of GMP laboratory operations. Ability to follow detailed procedures and work independently.
Analytical Skills: Need strong analytical abilities to identify and troubleshoot quality issues. They should be able to interpret and analyze data.
Problem-Solving Skills: Basic troubleshooting and problemsolving abilities.
Communication Skills: Strong communication and teamwork skills. They need to communicate effectively with team members, management, and external vendors to ensure everyone is aligned on quality standards.
Attention to Detail: Strong attention to detail for identifying potential quality issues and documentation accuracy.
Time Management: Effective time management and prioritization skills.
Preferred: Experience with LabVantage or similar LIMS, Empower 3, or similar data acquisition systems.
Bachelors Degree in Chemistry
Custom Fields:
Name: System Access Required
Value: Yes
Name: Badge ID Required
Value: Yes
Name: Supervisory Org
Value: QC Labs H(Ahmad Weeks)-60002819
Name: Invoice Type
Value: USA-ARL-Staffing-USD
Name: Workspace
Value: None
Name: Worker Time Type
Value: Full Time
Name: Work Desk Phone Number Required
Value: No
Name: Remote Worker
Value: No
Job ID: 519275180
Originally Posted on: 4/29/2026
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