Quality Assurance Engineer

Job Title

Key Responsibilities

Required Qualifications

Benefits

Pay

Schedule

The ideal candidate will have strong knowledge of FDA regulations, GMP, ISO standards, and quality management systems while collaborating with cross-functional teams to maintain the highest quality standards.

Key Responsibilities

• Perform quality inspections, manufacturing audits, and process reviews to ensure compliance with quality standards.
• Review batch records, device history records, and quality documentation for accuracy and regulatory compliance.
• Ensure compliance with FDA regulations, GMP, ISO 13485, and company quality management systems.
• Investigate quality issues, non-conformances, deviations, and customer complaints, and support CAPA activities.
• Participate in internal audits, supplier audits, and regulatory inspections while ensuring audit readiness.
• Collaborate with Manufacturing, Engineering, Regulatory Affairs, Validation, and Quality Control teams to improve product quality and manufacturing processes.
• Develop, review, and maintain quality procedures, SOPs, work instructions, and technical documentation.
• Support risk assessments, root cause analysis, change control, and continuous improvement initiatives.
• Monitor quality metrics and analyze trends to identify opportunities for process improvement and operational excellence.
• Ensure compliance with company quality policies and applicable regulatory requirements throughout the product lifecycle.

Required Qualifications

• Bachelor's Degree in Engineering, Biotechnology, Life Sciences, Chemistry, Biology, or a related scientific discipline.
• 2-5 years of Quality Assurance experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
• Strong knowledge of FDA regulations, GMP, ISO 13485, CAPA, Quality Management Systems (QMS), and regulatory compliance requirements.
• Experience performing quality inspections, manufacturing audits, documentation review, and quality investigations.
• Hands-on experience with deviations, non-conformances, root cause analysis, CAPA, and change control processes.
• Familiarity with quality documentation, batch record review, SOP development, and document control systems.
• Experience supporting internal audits, supplier audits, and regulatory inspections.
• Strong analytical, problem-solving, technical documentation, and organizational skills.
• Excellent communication and cross-functional collaboration skills with the ability to work effectively in a regulated environment.
• Experience working within pharmaceutical, biotechnology, or medical device manufacturing facilities is highly preferred.
• Knowledge of statistical quality tools, risk management methodologies, Lean Manufacturing, or Six Sigma is an added advantage.

Benefits

Details not specified.

Pay

Details not specified.

Schedule

Details not specified.