Production Supervisor


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


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


Bachelor´s Degree in related feiled


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.


Company: CGC-F-KSA
Department: Production
Job Location: Saudi Arabia
job type: Full Time
section: Section production

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