Responsibilities

• QC/ADL in Pharma or formulation Industry
• Well-versed in HPLC/GC analysis
• Preferably worked in MHRA/EU GMP/ US FDA plants
• Experienced in SOP writing, training, OOS management, Qualification of analytical instruments, validation of analytical methods.
• Capable of setting and implementation of Quality systems, sound knowledge of analysis and instrumentation techniques.

Skills & Knowledge

• Extremely organized with high attention to details
• Self-starter, capable of working with minimal direct supervision
• Good language and communication skills, particularly in English
• Capable of handling trouble shooting,
• Should have sound team spirit and ability to lead QC department

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