Marien Ciabal

QUALITY ASSURANCE SPECIALIST - Vonwelt Inc. Pharmaceuticals - Brgy. Sabang, Magdalena

(2025-06)

Conduct routine inspections in production per PIC/S and GMP; assist in implementing cGMP and regulatory guidelines; create regulatory signs for production.
Supervise and inspect finished goods; establish and implement batch-release and finished-goods inspection procedures; implement proper issuance of approved stickers from Quality to Production.
Create and design labels for better Quality Department organization; create work instructions for new forms and reports required for Production and Quality.
Review and update SOPs; ensure proper completion and authorization of documents prior to batch release; review old and new batch manufacturing records.
Analyze Quality Control (QC) reports to ensure results meet specified criteria; provide support in resolving product quality concerns; participate in product-related investigations and provide necessary support.
Assist colleagues with technical support issues and provide quality-related assistance as needed.
Facilitates GMP, GDP and Data Integrity to production workers.
Designs individual product packaging components, including packaging box artwork, blister layouts, and package insert layouts, ensuring compliance with regulatory, labeling, and GMP requirements.

INTERNSHIP - Vonwelt Inc. Pharmaceuticals - Brgy. Sabang, Magdalena

(2024-06 - 2024-08)

Assisted in testing raw materials and finished pharmaceutical products to ensure compliance with GMP and quality specifications.
Performed analytical procedures such as Loss on Drying (LOD), moisture analysis, hardness testing, friability testing, and other routine physicochemical evaluations required for product release.
Maintained accurate and complete laboratory documentation, ensuring traceability, data integrity, and proper recordkeeping for all tests performed.
Assisted in sample preparation, reagent/solution standardization, and laboratory housekeeping to maintain an organized and compliant testing environment.
Observed and followed proper safety procedures, chemical handling guidelines, and laboratory best practices to ensure a safe working environment.
Gained hands-on experience with pharmaceutical quality control workflows, regulatory requirements, and routine troubleshooting of analytical issues.

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