Responsibilities:
* Testing, review and disposition of pharmaceutical DSs, Intermediates, cleaning samples, investigatory samples, In Process Control (IPC) samples and/or raw materials in accordance with Corporate procedures and in compliance with the current GMP standards.
* Carry out testing of DSs, Intermediates, cleaning samples, investigatory samples, cleanrooms, IPC samples and/or raw materials in accordance with the valid testing procedures and regulatory requirements.
* Ensure that laboratory equipment is well maintained and calibrations are performed at the designated frequencies.
* Review results generated by other analysts for compliance with requirements.
* Ensure correct data entry to the current Laboratory Information Management System – SAP.
* Carry out method transfers and participate in the validation of analytical test methods as required.
* Write and maintain necessary documentation (test protocols, SOPs, instrumentation manuals and templates/check-out sheets, method transfer reports, OOS reports, etc.) according to the existing SOPs and cGMP standards.
Requirements:
* BSc in Scientific discipline.
* 2-4 years minimum work experience in the pharmaceutical industry.
* Experience in analytical testing techniques such as (HPLC, GC, UV, wet chemistry, dissolution, etc.).
* Experience with Good Manufacturing Practices and knowledge of analytical technologies.
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