Raajvi Tailor, Eit Email & Phone Number

United States

Greater Toronto Area Metropolitan Area

• Coordinated numerous facility and equipment validation projects by working with various clients• Lead air visualization studies of clean-rooms and equipment at a radio-pharmaceutical facility• Produced technical documents such as specifications and protocols for laboratory/packaging equipment and facilities systems • Efficiently prepared reports by analyzing and summarizing qualification results and checking for deviations and non-conformance• Proficiently worked with tight deadlines by keeping track of more than 3 projects using Microsoft Project • Supported process improvement activities for the business by developing a documents and projects archival system

Toronto, Canada Area

• Prepared SOPs for laboratory analytical equipment to ensure safe use• Supported the installation and maintenance of equipment to reduce delays of experiments• Designed and performed experiments for synthesis of lab-scale nano sheets for water treatment• Prepared presentations detailing test procedures and summarized results to further optimize design of experiments• Investigated potential solutions for clean energy storage systems and environmental remediation technologies

Toronto

• Optimized project schedules and process management requirements using Gantt charts and other Microsoft Excel based tools• Contributed in various aspects of validation, qualification and use of equipment for the analytical methods• Prepared and executed specifications, risk assessments and protocols/reports for validating analytical equipment and quality systems• Worked closely with fellow employees and management to fulfill 100+ requests for 2017 Global Quality Audit • Supported the Analytical Compliance Unit by gathering metrics regarding deviations and change controls • Supported Sample Receipt Activities by coordinating testing samples within 4 different departments• Supported quality process improvement activities and update of quality documents such as SOPs• Participated in routine activities by providing GMP documentation support for the department while implementing data integrity and quality assurance• Gained an understanding of the importance of data and process management in product development

Mississauga, Ontario, Canada

• Participated in maintenance of product formulas and quality control procedures to ensure they are accurate and provide maximum product fit for use• Demonstrated excellent laboratory skills by analyzing bulk batches and finished liquid/powder products while maintaining corresponding records• Demonstrated good time management skills by balancing adequate quality control testing with a high level of production and timely service to customers• Ensured all products are within specifications before leaving the facility, avoiding any performance failure and potential liability• Improved technical skills by reworking out-of-specs products and adjusting batch formulations without compromising quality

Oakville, On

• Developed technical laboratory skills by performing chemical analysis of raw material, packaging samples, in-process samples and drug products• Established knowledge of different laboratory instruments by assisting in the operation, preventative maintenance and calibration• Practiced safety and housekeeping of the laboratory

Oakville, On

• Improved documentation skills by effectively writing methods and keeping detailed records of protocols, reports and laboratory notebooks• Developed interpersonal skills by assisting with general administration in the Quality Services Department• Performed duties relative to collecting, washing, distributing and organizing of laboratory glassware and related supplies