Sterile QA Specialist: cGMP & Compliance

Julphar; United Arab Emirates; On-site; AED 120,000 - 150,000; Full time

Job summary

A pharmaceutical company in the United Arab Emirates is seeking a QA Specialist to ensure compliance with cGMP principles and manage quality control for sterile products. The ideal candidate will have a Bachelor's or Master's degree in Pharmacy and 3-5 years of quality operations experience. Responsibilities include enforcing compliance, participating in audits, and conducting quality checks to maintain high standards. This position offers a chance to contribute to a culture of quality and safety.

Qualifications

• Minimum 3-5 years of experience in quality operations within sterile manufacturing.
• Knowledge of EU Annex-1 and cGMP requirements.
• Strong command of English (written and spoken).

Responsibilities

• Ensure adherence to cGMP principles in all in-process quality checks.
• Participate in internal and external regulatory audits.
• Perform in-process quality checks according to SOPs.

Skills

Attention to detail

Communication skills

Collaboration skills

Results-oriented

Education

Bachelor’s or Master’s degree in Pharmacy

Tools

Agile

Trackwise

Ampelogic

Job description

A pharmaceutical company in the United Arab Emirates is seeking a QA Specialist to ensure compliance with cGMP principles and manage quality control for sterile products. The ideal candidate will have a Bachelor's or Master's degree in Pharmacy and 3-5 years of quality operations experience. Responsibilities include enforcing compliance, participating in audits, and conducting quality checks to maintain high standards. This position offers a chance to contribute to a culture of quality and safety.