Sinceritas is now accepting applications for the ‘Quality Manager’ position. Interested? Read more for details on responsibilities and needed qualifications.

RESPONSIBILITIES:

• Qualitative conduct of activities related to ISO 17025: 2006 standards’ implementation
• Validation cycles of laboratory instruments
• Chemical analyzes and tests as part of the Production, Quality Control, and R&D Departments
• Effective activities/programs in line with the regulatory standards and company policies, practices and processes
• Preparation, review and approval of ISO/IEC 17025:2006 documentation to ensure compliance with regulatory requirements, implementation and certification
• Assessing the impact of deviations and preventing future deviation
• Reviewing and approving ISO/IEC 17025:2006 changes in accordance with regulatory requirements
• Reviewing, approving and implementing staff training in accordance with ISO/IEC 17025:2006 requirements
• Resource management (people and resources) to meet organizational goals
• Ensuring timely (re)calibration of production equipment and quality control
• Ensuring final approval of new and validated methods in a timely manner
• Providing appropriate measures to monitor the progress of business goals to achieve desired results
• Providing support to the Quality Control Manager for a thorough evaluation of laboratory instruments, research, deviations and appropriate corrective/preventive activities to ensure they are handled appropriately; effective documentation is performed regarding the testing of raw materials, samples in process flow and final products
• Monitoring and controlling analytical data to confirm laboratory instruments give quality results and all instruments and systems are functioning properly
• Providing continuous improvement of quality systems and performance in the company through tools to improve processes and quality and by implementing new methods of analysis
• Performing various chemical analyzes and tests in the Production, Quality Control, and R&D Departments
• Supporting the Quality Assurance Department in GMP standards’ implementation
• Respecting and continually improving the company culture, where individuals can thrive in change
• Is included in ISU (Integrated Management System)
• Other responsibilities according to the qualifications and skills of the candidate

QUALIFICATIONS:

• University degree in Pharmacy or Chemistry, Master or Doctoral studies in Chemistry, or Specialist Studies in Pharmacy (testing and control of drugs or pharmaceutical technology) with a minimum of 5 years of relevant experience
• Direct experience and knowledge of quality management systems such as ISO/IEC 17025:2006, GMP etc.
• Previous experience with managing people and significant projects
• Proven skills in organizing and managing projects and must be able to balance priorities
• Proven previous experience in installing and inspecting laboratory equipment and instruments
• Excellent verbal and written communication skills; ability to share vision, guidance and data with colleagues at all levels and in a wide range of different working groups
• Excellent knowledge of English (written and spoken)

The Quality Manager’s working hours are Monday to Friday, 08:30 to 16:30 at the Sinceritas Production Facility in Rosoman, Kavadarci.

If interested in joining #TeamSinceritas, please send your updated resume to hr@sinceritas.eu with the subject line reading: Application for the Quality Manager’s position

За да го прочитате огласот на македонски јазик, Ве молиме кликнете тука: https://www.vrabotuvanje.com.mk/Rabota/404836/Menadjer-za-kvalitet/