Sterile QA Specialist: cGMP & Compliance Champion

Julphar; Ras Al Khaimah; On-site; AED 120,000 - 200,000; Full time

Job summary

A leading pharmaceutical company in Ras al-Khaimah is seeking a QA Specialist to ensure compliance with quality standards in sterile manufacturing. Responsibilities include overseeing quality checks, investigating deviations, and participating in regulatory audits. The ideal candidate should hold a Bachelor’s or Master’s degree in Pharmacy and have a minimum of 3–5 years of experience in quality operations. Join us to contribute to our mission of enhancing quality of life through excellence in healthcare.

Qualifications

• Minimum 3–5 years of experience in quality operations within sterile manufacturing.
• Knowledge of EU Annex‑1 and cGMP requirements.
• Proficient in computer applications and QMS systems.

Responsibilities

• Ensure adherence to cGMP principles in quality checks.
• Investigate deviations and support corrective actions.
• Participate in regulatory audits and documentation.

Skills

Results-oriented

Attention to detail

Strong communication skills

Organized and focused

Problem-solving abilities

Education

Bachelor’s or Master’s degree in Pharmacy

Tools

Agile

Trackwise

Ampelogic

Job description

A leading pharmaceutical company in Ras al-Khaimah is seeking a QA Specialist to ensure compliance with quality standards in sterile manufacturing. Responsibilities include overseeing quality checks, investigating deviations, and participating in regulatory audits. The ideal candidate should hold a Bachelor’s or Master’s degree in Pharmacy and have a minimum of 3–5 years of experience in quality operations. Join us to contribute to our mission of enhancing quality of life through excellence in healthcare.