Production Supervisor

دوام كامل في a Laimoon Verified Company في Saudi Arabia
نُشرت يوم November 11, 2024

تفاصيل الوظيفة

Overview

To create a quality system according to Pharmaceutical GMP regulations by means of SOPs, SMP, QMP, and 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 the quality system.

Responsibilities

Participation in dispensing of raw material.

Preparation of SOPs, BMR, formats, and protocols related to production.

Supervise all production activities such as cleaning, area maintenance, and providing accessories related to production.

Issuance of raw material and batch preparation.

Communication with the related department.

Participation in calibration and validation activities of processes and equipment.

Provide training to workers and operators.

Fill and check all BMR, formats, and log books.

Complete and meet daily and monthly production targets.

Qualifications

Bachelor's Degree in a related field.

Experience

Excellent spoken and written English language skills.

Proven working experience of a minimum of 2 years.

High attention to detail.

Able to meet strict deadlines.

Supervisory skills and experience.

Ability to perform physical tasks associated with sampling and inspecting.

Self-starter with critical thinking skills, able to multi-task and prioritize effectively.

Basic computer skills, including MS Word and Excel.

Experience in a cGMP environment preferred.

Good communication skills.

Proactive with planning skills.

Excellent analytical, problem-solving, and organizational skills.

#J-18808-Ljbffr Manufacturing & Production

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