Qualifications:

• Bachelor’s degree (S1) in Pharmacy or Chemistry

• Minimum 2 years of experience as a QC in the Medical Device industry

• Knowledge and practical implementation of ISO 13485 standards

• Detail-oriented and disciplined in following SOPs

• Experienced in maintaining accurate and well-organized quality documentation

• Strong communication and cross-functional collaboration skills

Job Description:

• Conduct sampling of raw materials and packaging materials in accordance with procedures

• Verify material compliance with standard specifications

• Monitor quality at each stage of the production process

• Ensure process parameters meet established standards

• Ensure products comply with quality specifications and regulatory standards before distribution

• Prepare inspection reports following ISO 13485 documentation standards