Christy Lanson Email & Phone Number

Ireland

• Conduct a range of standard microbiological analytical techniques, which include, but are not limited to, environmental monitoring, sampling and testing of WFI, growth promotion testing, TOC and conductivity testing.
• Carry out supportive tasks to ensure overall lab readiness, qualification of laboratory equipment, and validation of methods.
• Document experimental procedures and results in Electronic Laboratory Notebook (ELN).
• Adhere to current analytical practices as outlined in pharmacopoeias, specifications, regulations, and industry standards.
• Ensure proper housekeeping and Good Laboratory Practices (GLP) are upheld in the laboratory.
• Calibrate and upkeep all assigned laboratory instruments.

• Performing routine and non-routine analysis in GMP environment as requested by the Group Leader and Customer representative.
• Effectively testing pH and conductivity of water samples.
• Accurately performing the calibration and use of laboratory instrumentation
• Environmental Monitoring of ISO 5, ISO 6, ISO 7 and ISO 8 cleanrooms and isolators.
• Participating in all training required and scheduled in the Compliance Wire.
• Ensuring the development of SOPs and protocols in collaboration with the customer.

Ireland

• Performed production of pharmaceuticals in a GMP set up using manual and automated machines in line with standard operating procedures (SOP).
• Performed routine Quality Control testing including finished product analysis to ensure continuous process improvement.
• Planned and implemented procedures for mixing, filtration, packaging, and labelling pharmaceuticals, according to policy and legal requirements.
• Performed inventory control, completion of traceability documentation, stock entry and ordered the materials from other pharmaceutical companies.
• Actively performed sterilization of medical devices and equipment required for manufacturing of pharmaceuticals.
• Liaised with departments like Quality Assurance, Quality control, R&D, Marketing, Manufacturing, Analytical testing, Microbiology Analysis, Validation, and Warehouse.

Dublin, County Dublin, Ireland

• Performed the expression of recombinant protein 6-His-mCherry-EF2 in Escherichia coli BL21 expression system.
• The expression level of 6-His-mCherry-EF2 was optimised by optimising the concentration of Isopropyl β-D-1-thiogalactopyranoside (IPTG) the inducer, temperature and the induction time.
• Analysed the expression level of recombinant protein by Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis (SDS-PAGE) technology.
• Performed Immobilised Metal Affinity Chromatography (IMAC), and Size Exclusion Chromatography (SEC) on Fast Protein Liquid Chromatography (FPLC) for purification of recombinant protein with a Sephadex G 200 column.
• The concentration of the purified protein was determined by Nanodrop technology.
• Performed three rounds of Phage Display Technology on immuntubes to collect the mixture of phages that bound to the antigen.

• Manufactured medications prescribed by doctors and dentists by calculating, weighing, measuring, and mixing ingredients in accordance with current Good Manufacturing Practices and under Standard Operating Procedures.
• Dispensed up to 1000 prescriptions daily with 100% accuracy, managed, and improved the overall performance of the Pharmacy.
• Planned and implemented procedures for mixing, packaging, and labelling pharmaceuticals, according to policy and legal requirements, to ensure quality, security, and effectiveness.
• Advised patients and health care professionals about the rational use of drugs. Maintained high morale, integrity, respect, and a positive atmosphere.

Master Of Science - Ms, Biotherapeutics

Activities and Societies: Antibody discovery, Target Binding, ELISA, Western Blotting, Phage Display Technology, DNA Sequencing, PCR.

Bachelor'S Degree, Pharmacy

Have acquired knowledge in areas such as Organic Chemistry, Inorganic Chemistry, Pharmacognosy, Pharmaceutical Sciences, Medicinal.

Hsc, 98.6%

Ssc, Cgpa 10