Overview
To Créate 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
Responsibilities
Participation in dispensing of raw material.
Preparation of SOPs, BMR, Formats & protocols related to the production
To supervise all the production activities like cleaning, area maintaining, provide accessories Related to production
Issuance of raw material & Batch Preparation.
Communication with the related department
Participation in calibration & validation activities of processes & equipment
Provide training to the workers & operators.
To fill & check all the BMR, formats & log books
To complete & meet the daily & monthly production target
Qualifications
Bachelor´s Degree in related feiled
Experience
Excellent English language spoken and written.
Proven working experience minimum 2 years.
Having high attention to details.
Able to meet strict deadlines.
Supervisory skills and experience.
Ability to perform the physical tasks associated with sampling and inspecting.
Must be a self-starter with critical thinking skills and able to multi-task and prioritize effectively.
Basic Computer skills including using MS Word and Excel.
Experience in a cGMP environment preferred.
Have good communication skills.
Being proactive.
Have planning skills.
Excellent analytical, problem solving and organizational skills.