Responsibilities
- Supervise daily Quality Assurance activities to ensure compliance with GMP and regulatory requirements.
- Review and approve batch records, SOPs, validation protocols, and quality documentation.
- Ensure proper implementation of quality systems, policies, and procedures.
- Monitor deviations, investigations, CAPA, and change control processes.
- Support internal and external audits and regulatory inspections.
- Train and guide QA staff to maintain high-quality standards.
- Ensure compliance with data integrity and documentation practices.
- Collaborate with Production, QC, and other departments to resolve quality-related issues.
- Participate in risk assessments and continuous improvement initiatives.
- Ensure products meet quality standards before release.
Qualifications
- 5–10 years of experience in Quality Assurance within the pharmaceutical industry.
- Strong knowledge of GMP, regulatory requirements, and quality systems.
- Experience in handling deviations, CAPA, change control, and documentation review.
- Prior supervisory or team leadership experience preferred.
- Strong analytical and problem-solving skills.
- Excellent attention to detail and organizational skills.
- Good communication and reporting abilities.
Required Skills
- Communication Skills
Job Details
- Location Amman - Jordan
- Industry Healthcare and Pharmaceutical
- Job Type Full-Time
- Degree Bachelor
- Experience 5+
- Nationality Unspecified
Similar Jobs
We use cookies to ensure the proper functioning of our website. For an improved visit experience we use analysis products. These are used when you agree with "Statistics". Privacy statement
| Google Analytics | Create statistics data |
| Goal | _ga, _gat, _gid, _gali |