Sheena Persaud
Minneapolis,MN
Summary
Hardworking and passionate job seeker with strong organizational skills eager to secure the right job. Ready to help team achieve company goals. Detail-oriented team player with strong organizational skills. Ability to handle multiple projects simultaneously with a high degree of accuracy. To seek and maintain full-time position that offers professional challenges utilizing interpersonal skills, excellent time management and problem-solving skills.
Overview
14
14
years of professional experience
Work History
Validation Specialist
STERIS
03.2020 - Current
- Identified areas for improvement in existing validation systems, recommending changes that led to increased efficiency.
- Participated in external audits conducted by regulatory authorities demonstrating a high level of expertise and preparedness during inspections.
- Maintained excellent communication with stakeholders throughout validation projects, keeping them informed about progress and potential challenges.
- Ensured adherence to industry best practices by staying current on relevant guidelines such as FDA 21 CFR Part 11 and EU GMP Annex 15.
- Fostered a culture of continuous improvement by actively seeking feedback from team members, implementing process enhancements based on lessons learned.
- Conducted thorough root cause analyses to address deviations during validation activities, implementing corrective actions as needed.
- Led the training of junior team members on validation principles and techniques, fostering a culture of continuous learning within the organization.
- Reduced process variability with the development of robust validation protocols and procedures.
- Assisted in the preparation of regulatory submissions by providing validation-related documentation, contributing to successful approval outcomes.
- Enhanced product quality through rigorous testing and data analysis of manufacturing processes.
- Reviewed vendor-provided documentation critically assessing their capabilities in meeting project expectations before engaging in collaborations or outsourcing activities.
- Prepared detailed qualification documents including IQ/OQ/PQ protocols and reports for equipment and systems within regulated environments.
- Collaborated with cross-functional teams to ensure timely completion of validation projects, meeting regulatory requirements.
Laboratory Technician
STERIS
01.2011 - 03.2020
- Maintained a high level of accuracy in test results by following strict quality control procedures.
- Cleaned and sterilized tools and equipment to maximize purity of specimens.
- Operated basic laboratory equipment such as balances, pH meter, colorimeter, spectrophotometer, autoclave and evaporator.
- Performed testing and quality control using approved laboratory procedures and instrumentation.
- Maintained documentation on tests performed in lab.
- Contributed to a safe working environment by consistently following established safety procedures and guidelines within the lab setting.
- Documented information by maintaining daily logs and equipment record books.
- Kept laboratory supplies prepared by inventorying stock, placing orders and verifying receipt.
- Conducted routine equipment maintenance, ensuring optimal performance and reducing downtime.
- Prepared detailed documentation for each experiment, facilitating effective communication of results to colleagues and stakeholders.
- Collected and performed analytical testing on in-process product.
- Supported laboratory staff with advanced troubleshooting, resolving complex problems and helping with special projects.
Manufacturing Technician
STERIS
04.2010 - 01.2011
- Maintained a safe work environment by enforcing safety protocols and conducting routine inspections.
- Troubleshot equipment issues, minimizing downtime and keeping production on track to meet deadlines.
- Made sure that products were produced on time and are of good quality.
- Increased overall productivity by training new technicians and providing ongoing support to team members.
- Assembled and tested parts and components to meet safety and performance standards.
Education
Associate Degree - Accounting
University of Guyana
Georgetown, Guyana08.2008
High School Diploma -
Essiquibo Island Secondary
Guyana South America06.2006
Skills
- GMP Knowledge
- CAPA Management
- Equipment Qualification
- Process Validation
- Validation Protocols
- Cleaning validation
- Sterilization Validation
- Effective Communication
- FDA regulations
Timeline
Validation Specialist
STERIS
03.2020 - Current
Laboratory Technician
STERIS
01.2011 - 03.2020
Manufacturing Technician
STERIS
04.2010 - 01.2011
Associate Degree - Accounting
University of Guyana
High School Diploma -
Essiquibo Island Secondary
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