Open to opportunities

Syafira Tri Nurmalasari

@syafiratrinurmalasar

Data-driven quality improvement professional in manufacturing, combining pharmaceutical science, GMP expertise, and cross-functional leadership.

Indonesia

Message

What I'm looking for

I’m looking for a manufacturing role where I can drive quality improvement with data analysis, GMP/QA/QC rigor, and cross-functional collaboration. I want to strengthen quality systems, support corrective actions, and continuously optimize processes to improve product consistency.

I’m an emerging quality improvement professional with a strong background in pharmaceutical sciences and a focus on data-driven problem solving. I bring analytical thinking, leadership experience, and a continuous improvement mindset to manufacturing environments—especially where quality and consistency directly impact business outcomes.

In my current role as a Quality Associate (Quality Integral Program) at PT. Glotsar Indonesia, I analyze product quality performance data across manufacturing processes to identify trends, risks, and improvement opportunities. I support continuous improvement through root cause analysis, corrective action monitoring, and process optimization, while managing technical documentation, quality reports, and performance tracking for data-driven decision making.

Alongside this, I work as a Freelance Data & Documentation Specialist for multiple international clients. I organize complex information into clear, actionable formats, build structured databases and reports to improve workflow efficiency, and perform data review, validation, and quality checks to maintain accuracy and reliability.

My foundation includes laboratory and research experience through Universitas Islam Indonesia, where I supported formulation technology and GLP/SOP-based laboratory documentation. I also guided 30+ students and helped ensure smooth execution of 100+ practical laboratory sessions, and my master’s thesis covered end-to-end SNEDDS formulation development, stability testing, and quality parameter evaluation.

Experience

Work history, roles, and key accomplishments

Current

Quality Associate (QIP)

Current

PT. Glotsar Indonesia I

Dec 2025 - Present (7 months)

Analyzes product quality performance data across manufacturing processes to identify trends, quality risks, and improvement opportunities, supporting root-cause analysis and corrective action monitoring. Manages technical documentation and quality reports, and collaborates with cross-functional teams and international stakeholders on quality updates and readiness activities.

Data Quality Root Cause Analysis Process Optimization Technical Documentation Quality Reporting Cross functional Coordination Quality Systems GMP Data Validation

Current

Freelance Data & Documentation Specialist

Current

Upwork

Oct 2025 - Present (9 months)

Supports multiple international clients by managing research, data organization, and documentation projects with a focus on accuracy, consistency, and on-time delivery. Builds structured databases and reports, performs data review and validation, and delivers clear outputs from complex source information.

Data Structuring Documentation Research Structured Databases Report Writing data review Validation Information Structuring Client Communication

Laboratory Assistant

Universitas Islam Indonesia

Sep 2022 - Dec 2023 (1 year 3 months)

Assisted pharmaceutical laboratory activities, including formulation technology, microbiology, and pharmacology experiments, while following laboratory safety and compliance procedures. Prepared materials and experimental procedures, supported formulation preparation and sample handling, and maintained laboratory documentation according to SOP/GLP while guiding 30+ students.

Lab Safety GLP Lab Sample Handling Pre Formulation Data Collection Lab Documents Scientific Troubleshooting Scientific Data Interpretation

Research Assistant

Universitas Islam Indonesia

Aug 2020 - Mar 2021 (7 months)

Conducted formulation development research, including literature review, ingredient selection, experimental preparation, and formulation optimization. Performed formulation trials and testing (including physical characterization, stability evaluation, and quality assessment), and produced research documentation and technical reports following GLP principles.

Formulation Development literature review Quality Assessment Research & Documentation GLP Troubleshooting Formulation Challenges

Education

Degrees, certifications, and relevant coursework

Universitas Islam Indonesia

Master of Pharmaceutical Sciences, Pharmaceutical Sciences

2023 - 2025

Grade: GPA: 3.88 / 4.00

Completed a Master of Pharmaceutical Sciences degree focusing on end-to-end SNEDDS formulation development, including ingredient selection, emulsification process optimization, stability testing, and quality parameter evaluation (GPA: 3.88/4.00).