Quality Vacancy At Sunny Pharmaceuticals

GMP and Compliance– Sterile Pharmaceutical Manufacturing

Key Responsibilities

Monitor, assess, and ensure GMP compliance across sterile manufacturing, quality control, and support areas.

Lead internal audits, inspection readiness, and regulatory inspections.

Support deviation investigations, CAPAs, change controls, and risk assessments.

Provide GMP guidance to cross-functional teams and drive continuous quality improvement.

Maintain and improve quality systems in alignment with global best practices and data integrity requirements.

Review and approve GMP documents including SOPs, protocols, reports, and validation documentation.

Qualifications

Bachelors in Pharmacy or Science

1-5 years’ experience in GMP compliance in a sterile pharmaceutical

Deep knowledge of GMP guidelines (FDA, EMA, WHO), Annex 1, and data integrity standards

Strong communication, problem-solving, and auditing skills

Preferred Skills

Experience with regulatory inspections (FDA, EMA, etc.)

Lead auditor certification (ISO/GMP) is a plus

candidates can send CV to : eali@sunnyph.com, mentioned job title in the subject line. 

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