Analytical Technical Services Analyst At GSK Egypt
📌 Location: Cairo, Egypt
⬇️ Responsibilities:
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
– Validate analytical methods and cleaning verification methods according to approved protocols and regulatory expectations.
– Perform routine and non-routine testing of raw materials, packaging, intermediates, finished products and stability samples using validated methods.
– Operate, maintain and troubleshoot laboratory instruments such as HPLC, GC, UV/Vis, IR, atomic absorption and analytical balances.
– Prepare and standardize reference standards, reagents and solutions; keep accurate laboratory records and maintain data integrity.
– Support technical investigations, root cause analysis and corrective actions for out-of-specification results or equipment issues.
– Contribute to method transfers, prepare or update SOPs, and support knowledge sharing during product launches.
⬇️ Basic Qualification:
🔸Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biology or a related science field.
🔸0 to 3 years of practical laboratory experience in analytical testing, preferably in a regulated industry.
🔸Practical experience or training with common analytical instrumentation and laboratory techniques.
🔸Knowledge of good laboratory practice (GLP), good manufacturing practice (GMP) and basic environmental, health and safety (EHS) expectations.
– Basic computer skills and ability to use laboratory systems and standard office software.
– Effective communication skills in English and ability to work well in diverse teams.
⬇️ Preferred Qualification:
If you have the following characteristics, it would be a plus:
– Hands-on experience operating HPLC and GC with basic method troubleshooting skills.
– Experience with stability sample handling, stability programs or stability storage management.
– Experience in raw materials or packaging testing and supplier certificate of analysis review.
– Familiarity with Quality Management Systems and experience following or writing SOPs and technical protocols.
– Previous experience in a multinational or highly regulated environment.
– Strong attention to detail and a clear commitment to data integrity.