Manufacturing Operator with 2 years of experience in material dispensing, blending, and tablet compression in GMP environments. Proficient in adhering to batch records, SOPs, and quality standards to optimize pharmaceutical production. Recognized for strong attention to detail and effective equipment troubleshooting skills. Pursuing opportunities as a Documentation Technician.
Overview
3
3
years of professional experience
Work History
Batch Record Reviewer
AVARA
04.2025 - Current
Supported Quality Assurance with initial batch record checks during production stages.
Review manufacturing, dispensing, blending, compression, and coating batch records for completeness and compliance with cGMP.
Maintained strong attention to detail while reviewing numerous documents daily, ensuring consistent quality and accuracy.
Identify and escalate discrepancies, deviations, and missing information in real time.
Manufacturing Operator
Avara Pharmaceutical Services
06.2022 - Current
Weighed raw material accurately according to batch record instructions.
Operated blending machinery to mix raw materials per batch specifications.
Set up, operate, and monitor tablet press machine.
Perform in-process quality checks, such as tablet weight, thickness, hardness, friability, disintegration and record results accurately.
Assist in changeovers and troubleshoot issues to minimize downtime.
Clean and sanitize equipments and rooms between production runs per SOPs and cleaning check lists.
Trained new employees on company policies, equipment operation, and best practices, fostering a positive work environment and team cohesion.
Monitored and recorded batch data, ensuring compliance through proper documentation.
Collaborated in the creation and revision of Standard Operating Procedures (SOPs) for controlled tablet.
Assisted in the execution of trial batches and supported validation activities for controlled tablet.
Special Assignment In Engineering Department
Avara Pharmaceutical Services
11.2023 - 01.2025
Selected to support the Engineering Department on the purified water system generation integration, documentation, and technical data management.
Contributed to documentation and supported system qualification and validation activities.
Support internal audits and regulatory inspections on walk throughs and providing documentation.
Education
Bachelor of Science - Industrial Chemical Process
University of Puerto Rico
06-2022
Skills
Basic knowledge of cGMP, SOP, GLP, SDS and regulatory agencies
Demonstrated leadership capacity with ability to work in a fast pace teamwork orientated environment
Highly organized with attention to detail, ability to independently understand, follow, implement instructions and follow assignments to completion
Excellent command of computer software and platforms—MS Office (Word, Excel, PowerPoint, Outlook, Teams), ChemCad, Zoom etc
Proficient in analytical techniques and equipment such as: spectrophotometer, pH meter, balance, refractometer and other
Proficient in English and Spanish verbal and written communication
Timeline
Batch Record Reviewer
AVARA
04.2025 - Current
Special Assignment In Engineering Department
Avara Pharmaceutical Services
11.2023 - 01.2025
Manufacturing Operator
Avara Pharmaceutical Services
06.2022 - Current
Bachelor of Science - Industrial Chemical Process
University of Puerto Rico
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