Aditi Thakkar

• Successfully managed multiple projects simultaneously by prioritizing tasks according to urgency, resource availability, and alignment with organizational goals.
• Met project deadlines without sacrificing build quality or workplace safety.
• Established effective communication among team members for enhanced collaboration and successful project completion.
• HR related activities - creating performance review sheets and conducting performance review process, bookkeeping and pay transfers, maintaining leave records, hiring staff and initial screening interviews.
• Ensure that projects remain on-track to deliver their intended objectives

• Ensure that all the activities comply with ISO 13485:2003 Medical devices – Quality Management systems – Requirements for regulatory purposes
• Follow the GMP rules and regulations and ensure that all the products manufactured are according to the GMP rules and regulations
• Ensure the quality of each finished product on the microscope and check whether it is according to the quality standards and record the details of every lot and batch processed in the quality documentation records
• Maintain the cleanliness and hygiene of the laboratory space and perform general lab duties.

• Perform laboratory duties as required and make in-house ELISA kits to perform an assay
• As described earlier, in “Key Skills” the role ended within a week so it could not continue further.

• Ensure that all the activities comply with ISO 13485:2003 Medical devices – Quality Management systems – Requirements for regulatory purposes
• Follow the GMP rules and regulations and ensure that all the products manufactured are according to the GMP rules and regulations
• Assemble each product in different stages according to the work instructions manual of the product which is documented according to the company policy and standards
• Test each product after every stage of manufacturing and record the results in the quality management system designed especially for the related product
• Ensure all the products have undergone individual testing stages before they are placed for packing, ready for dispatch
• Maintaining and reviewing the quality documentation for each product is up to date before it is packed and ready for dispatch
• Maintaining a safe and well-organized working environment according to the company guidelines
• Assist with any other duty required in the production team.

• Work under the supervision of a NATA signatory to ensure all NATA accreditations are met
• Calibrate, maintain and repair of Thermo Fisher Scientific instruments to certified standards
• To be responsible for meeting customer requirements and expectations for accuracy and turnaround time based on determined service level agreements
• Communicate with internal and external customers on the progress of instrument calibration, maintenance, and repairs
• Meet and exceed the minimum call turnaround time for customers based on the service level agreement
• Complete calibration, maintenance and repairs according to QA and NATA accreditation
• Assist the service organization to meet and achieve its revenue target through the completion of calibration, maintenance, and repairs
• Providing customers with advice and technical support
• Actively work with the commercial organization to communicate customer’s needs
• Actively engage and support Thermo Fisher’s commercial team to achieve sales and margin (gross) targets by providing them with customer feedback and customer opportunities.

• Ensure that all the activities comply with ISO 13485:2003 Medical devices – Quality Management systems – Requirements for regulatory purposes
• Follow the GMP rules and regulations and ensure that all the products manufactured are according to the GMP rules and regulations
• Ensure the quality of each finished product on the microscope and check whether it is according to the quality standards and record the details of every lot and batch processed in the quality documentation records
• Maintain the cleanliness and hygiene of the laboratory space and perform general lab duties.

• Ensure that the SQAP always complies with ISO/IEC 17043 Conformity assessment – General requirements for proficiency testing
• Laboratory duties included preparation of specimens by pipetting different quantity aliquots, labelling and storing specimens in catalogued freezer system, performing primary testing (called as Safety screening) using ELISA assays, separation of blood components such as serum and plasma from blood as per requirement, maintenance and calibration of laboratory instruments such as pipettes, weighing scales, incubators, etc., daily, weekly as well as monthly monitoring of the fridges, freezers, and incubators, Specimen Database maintenance
• Assist with the packing of survey material and associated documentation for participants according to the different country regulations and requirements
• Assist with duties such as answering phone calls and emails regarding customer queries, accurate database management with record-keeping, release and culling the data of the surveys open and close, and other such general admin duties
• Perform Homogeneity and Stability studies and record associated documentation for QAP specimens
• Participate in the implementation and testing of new systems as well as maintain/improve existing systems
• Maintain and ensure the work environment is safe, clean and harmonious.

• Delicatessen assistant

• Front-end operator (Cashier)