Tanvi Suthar
Brampton,ON
Summary
Experienced in managing project portfolios, updating quality plans, and ensuring quality performance. Proficient in supporting product transfers from development to commercial operations, providing on-floor quality support, investigating deviations, participating in FMEA and process improvement initiatives.
Overview
6
6
years of professional experience
Work History
Packaging Technician
Thermo Fisher Scientific Inc.
04.2022 - Current
- Performed packaging tasks alongside team to demonstrate proper methods according to labor plan and assigned tasks.
- Labeled, recorded, and inspected packaging to prepare for shipment or storage.
- Performing IPT (In-process testing),Sensor challenges, AQL (Accepted quality level)
- Follow the EHS protocol, ensure the hazard identification in working environment.
- Knowledge of AlCOA, ALCOA+ RAPID investigation protocol
- Prepared orders for shipment by inserting associated paperwork, tagging boxes, and scanning barcodes to upload package data to tracking system.
Quality Assurance Analyst
Zydus Cadila Pharmaceuticals
07.2019 - 01.2022
- Experience in Good Manufacturing Practice (GMP) and QMS(Quality management system) compliance by identifying, reporting, proposing solutions and resolve issues and gaps.
- Experience in conducting investigations to identify the root cause of quality issues, CAPA processes and procedure to initiate CAPA to address quality issues.
- Proficient in using QA Oracle Agile software, LIMS, and ERP software.
- Conduct internal audit and client audit by providing required documentation of finished batch records
- Member of the Hazard identification group to ensure safety and preventive protocol in GMP environment.
- Approve and finalize new SOP and products according to client requirement.
- Maintain and execute track record, Batch Manufacturing Record (BMR), Master packaging Batch records (MBPRs), log books, Verification label, as per SOP for different Products and department, approve guideline for machine and production
- Review and finalize Certificate of Analysis (CofA) for In process Quality Control.
- Responsible for all documentation related to bulk and finished product, collected and compiled a documents before release, execution of releasing final documents for a various departments.
Quality Control Chemist
Meck pharamacutical & chemical PVT LTD
08.2018 - 06.2019
- Analyze pharmaceuticals analyte from processing to final stage of product by different test method
- Perform wet analysis of in process compound by moisture ( Karl Fischer), PH, Sulphate ASH, assay,
- LOD(Loss on drying), TLC ( Thin layer Chromatography),
- Perform raw material analysis by GC.
Education
Master of Science - Forensic Science
Gujarat University
05.2018
Bachelor of Science - Chemistry
Gujarat University
05.2016
Timeline
Packaging Technician
Thermo Fisher Scientific Inc.
04.2022 - Current
Quality Assurance Analyst
Zydus Cadila Pharmaceuticals
07.2019 - 01.2022
Quality Control Chemist
Meck pharamacutical & chemical PVT LTD
08.2018 - 06.2019
Master of Science - Forensic Science
Gujarat University
Bachelor of Science - Chemistry
Gujarat University
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