شركة أدوية كبرى تفتح أبوابها للكفاءات المتمكنة

شركة أدوية كبرى تفتح أبوابها للكفاءات المتمكنة من إدارة الأنظمة والجودة

شركة أدوية كبرى تفتح أبوابها للكفاءات المتمكنة من إدارة الأنظمة والجودة

Jordan Sweden Medical is looking to hire a Compliance Supervisor with the following requirements:

– BSc in Chemical or Industrial Engineering- Minimum of 7 years of experience working in the pharmaceutical industry including a minimum of 3 years in the quality assurance field

– Courses in Good Manufacturing Practices, quality systems management and Total Quality Management

– Knowledge in quality tools and process improvement tools

– Knowledge in JFDA and relevant

international regulatory requirements- Auditing and inspection skills

– Statistical and analytical skills-

Strong verbal and written communication and problem-solving skills

– Preferable knowledge and courses in ISO 9001

– Good command of English language

– Strong computer skills including Microsoft Office and databasesThe candidate will be responsible for:

– Reviewing and analyzing the quality management systems and related work methods in all departments for enhancement and compliance purposes.

– Evaluating the activities of responding to inspection reports and assessing responses to ensure compliance to regulatory requirements.

– Supervising and participating in the required investigations resulting from external audits and inspections, customer complaints, or any assigned projects, and following up on the corrective and preventive actions as requested and needed.

– Management of the change control system of the company.

– Scheduling and following up on executing the studies required for the risk evaluation and assessment of operations and systems according to risk schedule.

– Scheduling and following up on compliance and spot audits and following up on the corrective and preventive actions to ensure their effectiveness.

– Evaluating contract agreements requirements and directing departments to formalize service agreements, and ensuring agreements are compliant with regulatory requirements and industry standards.

– Scheduling and following up on performing supplier evaluations and risk assessments.

– Supervising the auditing process of suppliers and service providers according to the established and followed plan and procedures.

– Handling and implementing the GMP training program and participating in employees training on cGMP principles according to the annual cGMP training schedule.

– Participating in quality improvement projects in the company.

Candidates should send their resumes to the following email address and add the position in the

title:[email protected]