Japloe Sneh
CSV Specialist at Porton Biopharma Ltd- Claim this Profile
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English Native or bilingual proficiency
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German Elementary proficiency
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Latin Limited working proficiency
Topline Score
Bio
Credentials
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JavaScript Algorithms and Data Structures
freeCodeCampApr, 2022- Oct, 2024 -
Responsive Web Design
freeCodeCampMar, 2022- Oct, 2024
Experience
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Porton Biopharma Ltd
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United Kingdom
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Pharmaceutical Manufacturing
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1 - 100 Employee
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CSV Specialist
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Nov 2020 - Present
Working within the Validation team to manage and execute validation activities associated with the cGMP compliance of computerised and software systems, ensuring that they are appropriately qualified and fit for operational use. Responsibilities include: • Taking the lead in computer system validation and compliance, to manage and deliver specific Validation Projects according to the business priorities, including work scheduling and supervision of junior members of staff. • Working both independently and within the matrix management system • Continuous improvement of validation systems and procedures to ensure efficiency and best practice within the industry and to stay abreast of changing regulatory expectations. • Writing, reviewing and approving validation documentation including protocols and reports and managing the timely closure of any discrepancies or non-conformities. • Providing a reliable service to internal customers to ensure that timescales are met and work is carried out to meet expectations. • Maintaining the ongoing compliant status of computer systems associated with equipment, facilities and utilities by involvement of the scheduling of activities. • Communicating validation activities with internal and external customers and working with them to resolve problems and conflicts.
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Recipharm
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Sweden
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Pharmaceutical Manufacturing
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700 & Above Employee
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IT Solutions Support Specialist
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Jan 2019 - Nov 2020
Computer Support Specialist for the laboratories, providing technical assistance and support, in addition to managing the systems. Also supported and managed several systems outside of the lab. Responsibilities included: Maintenance of SAP-QM Module Business Administrator for TrackWise EQMS System Administration and Maintenance of Waters Empower CDS System administrator for all other lab software packages on-site, including LabX 3.1, Spectrum 2, WinLab, TruScan 2.6.0, AACE 7.01 GLP, Tiamo 2.5, Agilent Dissolution Workstation Development of Spreadsheet tools. Computer Systems Validation Office 365 Business Champion Writing and maintaining administration procedures Data Integrity Assessments of Lab Systems
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Aesica Pharmaceuticals Ltd
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United Kingdom
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Pharmaceutical Manufacturing
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100 - 200 Employee
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Analytical Development Scientist
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Sep 2017 - Jan 2019
Worked as an Analytical Development Scientist responsible for providing analytical support to secondary manufacturing, new business development activities, and to the technical project teams. Responsibilities included:Test method transfers, test method development & validation of methods for raw materials, intermediates, finished products, and cleaning samplesProcess validation testing of new business productsDevising, developing, and operating analytical test methods to provide information required for development projectsTesting and technical support of development, commercial and stability samples through the product life cycleIdentifying requirements for new analytical equipment and facilitate its introductionProduction of documentation in support of analytical method verification/validation and method transfer activities including Validation Protocols and Reports.Providing support to cost proposal generationEmpower Method Development SME for the team.
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QC Analyst
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Jan 2016 - Sep 2017
Worked as a Quality Assurance Pharmaceutical Analyst trained in HPLC, GC, UV-Vis Spectroscopy, IR Spectroscopy, Karl Fischer Titration, Wet Chemistry, and Dissolution testing.Responsibilities included:Undertaking analysis of in-process and final stage finished productsTesting raw materials and APIs using various wet chemistry techniquesPerforming accurate and reliable laboratory tests and generating, reporting and approving results to GMP standard, in accordance with current company requirements and SOPs.
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Spires Academy
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Education Administration Programs
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1 - 100 Employee
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Science Technician
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Mar 2014 - Dec 2015
Worked as a Science Technician. Responsibilities included: Managing the school laboratories, classrooms, preparation room, and chemical stores Maintaining and repairing equipment Supporting teaching staff and students during lessons Performing risk assessments and carrying out health and safety checks Organising and store equipment and checking stock levels Ordering resources and managing budgets Worked as a Science Technician. Responsibilities included: Managing the school laboratories, classrooms, preparation room, and chemical stores Maintaining and repairing equipment Supporting teaching staff and students during lessons Performing risk assessments and carrying out health and safety checks Organising and store equipment and checking stock levels Ordering resources and managing budgets
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University of Leeds
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United Kingdom
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Higher Education
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700 & Above Employee
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Graduate
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Sep 2009 - Feb 2014
Modules studied included: Structure and Reactivity in Inorganic Chemistry, Organic Structure, Mechanism and Synthesis, Foundations of Physical Chemistry, Chromatography and Analytical Separation Dissertation (5000 Words): Supercritical Fluid Chromatography - Discussed the concept of supercritical fluids its use in chromatography. Industrial Report (15,000 Words): A detailed report on the placement, including a detailed discussion of the protein binding project, preparatory and purification work and the theory and practical skills gained. Master’s Thesis (10,000 Words): Photoelectrical Reduction of Nitro Compounds on Semiconductor Nanoparticles – A detailed report of investigations into the use of titanium dioxide nanoparticles for the reduction of nitro compounds.
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Cellzome
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Chemical Analyst
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Jul 2011 - Jun 2012
Worked full-time as an analytical chemist, responsible for the purification of organic compounds. The year was a fantastic success and by its completion over three hundred compounds were purified, several of which were progressed to in vivo studies. Also set up an exceptionally beneficial proprietary analytical service, took over the responsibility of maintaining the HPLC machines and gained a hands on experience of the various aspects of a pharmaceutical laboratory. Worked full-time as an analytical chemist, responsible for the purification of organic compounds. The year was a fantastic success and by its completion over three hundred compounds were purified, several of which were progressed to in vivo studies. Also set up an exceptionally beneficial proprietary analytical service, took over the responsibility of maintaining the HPLC machines and gained a hands on experience of the various aspects of a pharmaceutical laboratory.
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Tender Loving Carers Ltd
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Whitstable
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Domiciliary Carer
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Feb 2009 - Aug 2010
Position taken up during my gap year. Was responsible for personal and domestic care. Took first aid, food preparation and manual handling training. Position taken up during my gap year. Was responsible for personal and domestic care. Took first aid, food preparation and manual handling training.
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Education
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2009 - 2013
University of Leeds
Master's degree, Chemistry -
2001 - 2008
Simon Langton Girls' Grammar School
A-Levels, Biology, Chemistry, Physics
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