On-Site Receipt Validation Specialist

Tada, Inc.; Cibinong; Hybrid; IDR 133,920,000 - 223,200,000; Full time

Benefits offered by this job

Salary with bonus opportunities

Health, dental, and vision insurance

Retirement savings plan

Paid time off

Job summary

Our client is seeking an experienced Quality Assurance Auditor to join their Depok operations. This hybrid role requires on-site presence for key audits and remote capabilities for report generation and follow-up.

You will assess compliance with GMP, GCP, GLP, and other quality standards across pharmaceutical operations. Your work will help maintain product quality, regulatory compliance, and the integrity of manufacturing and research processes.

Qualifications

• Bachelor's degree in Pharmacy, Chemistry, Engineering or related field.
• Minimum of 4 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
• Proven experience in conducting audits, with a strong understanding of regulatory requirements.
• Excellent knowledge of pharmaceutical manufacturing processes and quality systems.
• Strong analytical, problem-solving, and report-writing skills.
• Ability to work effectively both independently and as part of a team, balancing remote and on-site duties.

Responsibilities

• Plan and conduct internal and external audits of manufacturing facilities, laboratories, and clinical sites.
• Evaluate adherence to GMP, GCP, GLP and other applicable quality system regulations.
• Identify non-compliance issues, assess risks, and recommend CAPAs.
• Prepare detailed audit reports documenting findings, observations, and recommendations.
• Follow up on CAPAs to ensure timely and effective implementation by auditees.
• Contribute to the improvement of the Quality Management System (QMS).

Skills

Auditing

GMP

GCP

GLP

CAPA

QMS

Report writing

Analytical thinking

Teamwork

Education

Bachelor's degree in Pharmacy, Chemistry, Engineering

Job description

Our client is seeking an experienced Quality Assurance Auditor to join their operations in Depok . This hybrid role requires both on-site presence for key audits and remote capabilities for report generation and follow-up. You will be responsible for assessing compliance with Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), and other relevant quality standards across various pharmaceutical operations. Your work will be crucial in maintaining product quality, ensuring regulatory compliance, and upholding the integrity of our client's manufacturing and research processes.

About the Role

Our client is seeking an experienced Quality Assurance Auditor to join their operations in Depok . This hybrid role requires both on-site presence for key audits and remote capabilities for report generation and follow-up. You will be responsible for assessing compliance with Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), and other relevant quality standards across various pharmaceutical operations. Your work will be crucial in maintaining product quality, ensuring regulatory compliance, and upholding the integrity of our client's manufacturing and research processes.

Key Responsibilities

• Plan and conduct internal and external audits of manufacturing facilities, laboratories, and clinical sites.
• Evaluate adherence to GMP, GCP, GLP , and other applicable quality system regulations.
• Identify non-compliance issues, assess risks, and recommend corrective and preventive actions (CAPAs).
• Prepare detailed audit reports documenting findings, observations, and recommendations.
• Follow up on CAPAs to ensure timely and effective implementation by auditees.
• Contribute to the improvement of the Quality Management System (QMS).

Requirements

• Bachelor's degree in Pharmacy, Chemistry, Engineering, or a related scientific field.
• Minimum of 4 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
• Proven experience in conducting audits, with a strong understanding of regulatory requirements.
• Excellent knowledge of pharmaceutical manufacturing processes and quality systems.
• Strong analytical, problem-solving, and report-writing skills.
• Ability to work effectively both independently and as part of a team, balancing remote and on-site duties.

Benefits

• Competitive annual salary and bonus opportunities.
• Comprehensive health, dental, and vision insurance.
• Retirement savings plan.
• Paid time off, including vacation and sick days.
• Opportunities for professional development and further certifications.
• A collaborative environment focused on ensuring the highest quality standards in Depok .