Position: Quality Control Associate
Department: Quality Control
Location: [Company Location]
Reports to: Quality Control Manager
Experience: 0-2 years
Job Summary:
As a Quality Control Associate in the Quality Control function for the Chemical domain, you will be responsible for ensuring that products meet the required quality standards. You will conduct various tests and inspections, analyze data, and support the continuous improvement of quality control processes. This role requires a fundamental understanding of chemical principles, attention to detail, and the ability to work collaboratively in a team environment.

Key Responsibilities:
Conduct routine and non-routine analyses of raw materials, in-process formulations, and finished products to ensure quality standards are met.
Perform laboratory tests using standard operating procedures (SOPs) and Good Laboratory Practices (GLPs).
Document and interpret test results, and report findings to the Quality Control Manager.
Assist in the development and validation of new analytical methods.
Maintain and calibrate laboratory instruments and equipment.
Participate in root cause analysis and corrective action investigations for non-conforming products.
Ensure compliance with all safety, health, and environmental regulations.
Prepare detailed reports and maintain accurate records of all quality control activities.
Collaborate with cross-functional teams to support continuous improvement initiatives.

Qualifications:
Bachelor's degree in Chemistry, Chemical Engineering, or a related field.
0-2 years of experience in quality control or a related field.
Basic understanding of chemical principles and quality control procedures.
Proficiency in using laboratory equipment and software for data analysis.
Strong organizational skills and attention to detail.
Excellent written and verbal communication skills.
Ability to work effectively both independently and as part of a team.

Preferred Qualifications:
Experience with specific chemical analysis techniques (e.g., GC, HPLC).
Familiarity with quality management systems and regulatory standards.
Knowledge of Good Laboratory Practices (GLP) and ISO standards.