Tajeram Deodat
Gaithersburg,MD
Summary
Quality professional with exceptional background in QA,QC & QO.
Overview
3
3
years of professional experience
1
1
Certification
Work History
QA Coordinator (Contractor)
CenExel Pharma
Gaithersburg, MD
08.2025 - 01.2026
- Assists the QA Manager in the development, implementation and follow-up of quality assurance programs including necessary or appropriate policies and guidelines.
- Reviews follow-up monitoring visit reports, protocol deviation logs, and quality findings trackers for trend analysis.
- Performs ongoing review of a percentage sampling of study inclusion/exclusion, study procedure records, and laboratory reports to ensure that they are conducted according to the protocol, applicable SOPs, ICH/GCP guidelines and federal regulations.
- Performs quality review of initially created source documentation, including amendments, to ensure all protocol required procedures are present.
- Provides training and education on SOPs, GCP, and federal regulations as appropriate.
- Prepares for internal and external audits and FDA inspections.
- Attend site initiation visits, as needed.
- Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working practices, protocol, and company guidelines and policies.
QA Batch Record Reviewer
Catalent Pharma
Harmans, MD
04.2025 - 10.2025
- Ability to quickly process complex information and make critical decisions with limited information required.
- Collaborate within Manufacturing to resolve batch record discrepancies or errors as it relates to Good Documentation Practices or Manufacturing Execution System (MES) inventory.
- Communicate effectively with cross functional departments to ensure on time delivery of QA review and disposition.
- Responsibilities
- Compile and report performance metrics for Batch Review and Release.
- Contributes to process improvement of batch records and associated processes (e.g. turnaround times) to ensure all QA batch disposition deadlines are met.
- Critically review various documentation types to ensure completeness, accuracy and compliance including but not limited to test methods, method validation protocols and reports and SOPs.
- Identify and participate in internal quality improvement initiatives: evaluate internal processes, suggest/design/implement improvements, create/revise relevant SOPs.
- Independently executes batch record review for completeness, accuracy and cGMP compliance.
- Maintain reporting elements (metrics) for individual Quality and Quantity of daily assignments.
- Oversee status of batches through disposition/release process and remove barriers, communicate escalations as Appropriate.
- Participate in site and corporate quality and process improvement initiatives. Represent MFG on project teams and represent the Batch Disposition manufacturing perspective as needed.
- Perform duties under limited supervision and according to standard operating and manufacturing procedures.
- Perform tasks in a manner consistent with all Catalent policies including safety (EHS), quality systems and cGMP requirements.
- Prepare reports right the first time (RFT) reports and keep upper-level management informed of progress as manufacturing reviewer for investigations, deviations and CAPAs appropriate and designated by QA Management.
- Review documentation for manufacturing activities associated with commercial, development, and engineering execution in accordance with good documentation practices (GDP), including but not limited to: executed batch records, master batch records, product labels, SMPs, and product specific documents.
- Support on-the-floor quality issues in a timely manner, documentation of all events/investigations and required immediate escalation.
- Support the evaluation and lot disposition of intermediates, finish bulk drug substance and drug product.
- Understand risks and delays to batch release and communicate appropriately.
Quality Technician level III
Meso Scale Diagnostics, LLC
Rockville, MD
07.2023 - 04.2025
- Review of QC and GDP Batch Record Data.
- Carry out Dispositions Tasks and Sample release.
- Upload all GDP Batch records into SharePoint System.
- Inspect and receive incoming raw materials and file associated paperwork.
- Carry out inventory and Log tickets faulty lab equipment.
- Aid in lab walkthrough inspections.
- Maintain up-to-date Release Pass/Hold/Fail tag on all Inventories intended for customers or related for quality testing and ensure correct physical location of inventory in Quarantine or on Hold.
- Inventory or cycle count on QC testing materials.
- Monitor Temperature Charts or Data loggers.
Education
Upstream and Downstream Biomanufacturing
Montgomery College
05.2024
Transformative Leadership
Shenandoah University
02.2024
BSc - Pharmacy
University of Guyana
01.2007
Skills
- Flexibility
- Training and mentoring
- Laboratory skills
- Scientific writing
- Data collection
Certification
- Human Subject Research (1. Basic Course) Citi Program certification
- Good Clinical Practice. Citi Program certification
- Information Privacy and security. Citi Program certification
- Responsible conduct of research. Citi Program certification
- Conflict of interest. Citi Program certification
- OSHA Blood Borne Pathogens. Citi Program certification
- GCP of Clinical trials with investigational drugs and Biologics. Citi Program certification
- Aseptic Techniques and GMP
- Supply Chain Management for Pharmacists (Georgetown public Hospital & FDA Guyana)
- Patient Counselling Basics of patients for Pharmacist (NAPS)
- Law Enforcement, Self Defense tactics, CPR and first aid, patrol
Timeline
QA Coordinator (Contractor)
CenExel Pharma
08.2025 - 01.2026
QA Batch Record Reviewer
Catalent Pharma
04.2025 - 10.2025
Quality Technician level III
Meso Scale Diagnostics, LLC
07.2023 - 04.2025
Upstream and Downstream Biomanufacturing
Montgomery College
Transformative Leadership
Shenandoah University
BSc - Pharmacy
University of Guyana