
OPEN POSITION: Quality Manager
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/