To Cr\u00e9ate Quelite Sistema according to Pharmaceutical GMP regulations y means of SOPs, SMP, QMP, CMP plan, organize, and supervise the activities of auditing, in-process inspection in manufacturing and packaging, and quality assurance administration to ensure regulatory compliance and maintain proper documentation of quality system<\/p>\n
Participation in dispensing of raw material.<\/p>\n
Preparation of SOPs, BMR, Formats & protocols related to the production<\/p>\n
To supervise all the production activities like cleaning, area maintaining, provide accessories Related to production<\/p>\n
Issuance of raw material & Batch Preparation.<\/p>\n
Communication with the related department<\/p>\n
Participation in calibration & validation activities of processes & equipment<\/p>\n
Provide training to the workers & operators.<\/p>\n
To fill & check all the BMR, formats & log books<\/p>\n
To complete & meet the daily & monthly production target<\/p>\n
Bachelor\u00b4s Degree in related feiled<\/p>\n
Excellent English language spoken and written.<\/p>\n
Proven working experience minimum 2 years.<\/p>\n
Having high attention to details.<\/p>\n
Able to meet strict deadlines.<\/p>\n
Supervisory skills and experience.<\/p>\n
Ability to perform the physical tasks associated with sampling and inspecting.<\/p>\n
Must be a self-starter with critical thinking skills and able to multi-task and prioritize effectively.<\/p>\n
Basic Computer skills including using MS Word and Excel.<\/p>\n
Experience in a cGMP environment preferred.<\/p>\n
Have good communication skills.<\/p>\n
Being proactive.<\/p>\n
Have planning skills.<\/p>\n
Excellent analytical, problem solving and organizational skills.<\/p>\n
<\/p>\n","protected":false},"excerpt":{"rendered":"
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