Scientific Recruitment Consultant
SRG
Total years of experience :14 years, 3 Months
o Working under cGMP/GLP.
o HSE Forum member.
o Training of new analysts.
o Audited by International health authorities and regulatory bodies such as FDA, MHRA, ANVISA, KFDA.
o Performing analysis of drug substances (using analytical methods including HPLC, GC, TLC, Karl Fisher, Wet Chemistry,
FTIR, UV, XRF, ICP) and investigating their compliance with specifications.
o Writing up of results and reports, presenting findings to management.
o Secondary checking write-ups and analysis performed by other analysts.
o Participating in OOE/OOS root cause investigations.
o Calibrating and maintaining lab equipment and instruments, and participating in troubleshooting investigation and
problem solving to ensure compliance with cGMP, GLP, GxP and SOPs.
o Achievement of district sales and margin targets of Automation product portfolio.
o Sales and promotion of the company's Automation product range.
o Ensuring that all current promotions are actively promoted to appropriate target customers throughout the territory.
o Maintaining, expanding and updating the company's customer database.
o Use the company's business tools to help drive territory sales and margin, including the customer database, business
analysis and sales process tools.
o Working under cGMP/GLP.
o Performing analysis (including: Oxygen Content, Volatile Matter, Content Uniformity, Impurities, and Dissolution testing)
of Buprenorphine products (controlled drugs), and investigating their compliance with specifications and SOP.
o Writing up of results and reports, presenting findings to management.
o Calibrating and maintaining lab equipment and instruments, and participating in troubleshooting investigation and
problem solving to ensure compliance with cGMP, GLP, and SOPs.
o Working under cGMP/GLP.
o Calibrating and maintaining lab equipment and instruments, and participating in troubleshooting investigation and
problem solving to ensure compliance with cGMP, GLP, and SOP.
o Establishing a suitable stability-indicating methodology (using HPLC) for a newly formulated Hydroquinone cream product
manufactured in the production unit of Guy's & St. Thomas' NHS foundation trust.
o Validating the established stability-indicating methodology according to the ICH Q2 (R1) and NHS SOP validation criteria.
o Performing the validated stability-indicating methodology on the Hydroquinone cream product and assigning a shelf-life
to the product.
to Diabetologists, Endocrinologists,
Cardiologists and GPs.
o Managing region and setting business plans, sales forecasts, accounts potentiality profiles, round table
discussions, preparing business reports and presentations.
o Weekly and monthly progress reviewed in meetings with senior management.
o Maintaining knowledge of new developments in Modern Insulin, anticipating impacts on business and adapting strategies
accordingly.
o Monitoring competitor activities and strategies.
* Novo Nordisk: DTP "Direct To Patients" program Team Leader
* Responsibilities:
70.92%). * Cambridge International
,