I Singh Email and Phone Number

Supported the Quality Team in maintaining Compliance of the Quality processes and documentation on site to meet the requirements of the Notified Bodies/UKAS• Support continuous improvements in the Quality Management System (QMS) to drive improvements to processes and making lean processes to minimise time waste• Updating and maintaining the QMS-Computer Systems Validation experience• Work with the managers and their teams to maintain all aspects of the QMS e.g. Change… Show more Supported the Quality Team in maintaining Compliance of the Quality processes and documentation on site to meet the requirements of the Notified Bodies/UKAS• Support continuous improvements in the Quality Management System (QMS) to drive improvements to processes and making lean processes to minimise time waste• Updating and maintaining the QMS-Computer Systems Validation experience• Work with the managers and their teams to maintain all aspects of the QMS e.g. Change Controls, Non Conformities, CAPAs, Customer Complaints/ Working and Assisting with Incident Officer to close severe non-conformities.• Worked with other QA staff to provide all the support required by the Operations teams, e.g. Work Instruction review, report review, QA statements, training, quality record review.• Performed internal audits according to the provided schedule.• Performed desk-based and on-site audits of sub-contractors and suppliers.• Provided support to ensure timely release of results and audited reports to clinicians.• Organised and implemented training of new personnel on all aspects related to the QMS.• Supported the collection and reporting of monthly Quality KPIs.• Maintained thorough knowledge and understanding ISO 15189 requirements, Regulatory expectations and guidance documents as these pertain to the work performed on site• Adopted a safe behaviour by exercising due regard for the health and safety of myself, colleagues and clients, in line with the company’s policies and procedures. Show less

Maintenance of the QMS, audit schedule, auditing. Compliance against ISO 17025, 17020, 14001, 45001UKAS external audit demonstrator Breakdown of Non-conformities across the businessmeasurements of CAPAs and effectiveness of the actions.Creation of KPIs for the quality department which is available for all key internal and external stakeholdersManagement of Quality Officers. Proficient in Microsoft applications (office) and QMS system.

Human Pharmaceutical and Veterinary Quality Analysis

laboratory analysis of pharmaceutical products including report writing. Working to GMP guidelines and in accordance to MHRA

Duties involve working with highly sensitive information. Please ask direct if required.laboratory and office based

Supervisory position- management of checkout team

Analytical scientist, analysing total inorganic carbon from particular water sources across the country to meet environmental legislation

FTIR, UV, HPLC, thin layer chromatography, wet chemistry, titrations, melting point verification. GMP/GLP, Method development, following SOPs.Following appropriate pharmacopoeia-BP, Ph eur etcTesting the active ingredients of prescription drugs to prove methods adapted from pharmacopoeias are safe and quality assured to make them into suspensions. The pharmacist will further check the final product which will enable the suspensions to be dispatched to the pharmacies then to the… Show more FTIR, UV, HPLC, thin layer chromatography, wet chemistry, titrations, melting point verification. GMP/GLP, Method development, following SOPs.Following appropriate pharmacopoeia-BP, Ph eur etcTesting the active ingredients of prescription drugs to prove methods adapted from pharmacopoeias are safe and quality assured to make them into suspensions. The pharmacist will further check the final product which will enable the suspensions to be dispatched to the pharmacies then to the patient. Show less