QA 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, 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 & protocols related to the production.

Supervise all production activities like cleaning, area maintenance, and 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.

Fill & check all BMR, formats & log books.

Complete & meet the daily & monthly production targets.

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 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.

Good communication skills.

Proactive with planning skills.

Excellent analytical, problem-solving, and organizational skills.

#J-18808-Ljbffr Quality Management & Operations

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