QC Instrument Expert Global Pharma Manufacturing Site Pest County

Budapest - Hungary

Monthly Salary: Not Disclosed

Posted on: 10 hours ago

Vacancies: 1 Vacancy

Job Summary

Supporting a special field we are looking for an ambitious and broad-minded person on behalf of our global partner who manufactures solid pharmaceutical products in this position you will be the taskmaster of the sites entire QC instrument park and you will be responsible for ensuring the availability of the machines.
For investment projects you play a determinative role in the procurement process of the new machine park and the support during the installation period. Day-to-day work requires close cooperation with internal and external departments such as supplier companies or QC Managers.

Your key responsibilities:

Create and continuously update documentation related to the inspection of devices and processes within your area of control
Design validation plans for computer systems used in product quality control tests
Prepare calibration and qualification plans and reports for analytical instruments
Ensure quality assurance perspectives are considered when ordering new equipment and defining user requirements (URS)
Collaborate in the development of procedures and the commissioning of instruments
Follow implement and continually improve data integrity guidelines within quality control
Participate in the development of economic and efficiency indicators characteristic of the area (data provision and analysis)
Continuously monitor the GMP requirements ensure compliance and provide necessary training and updates
Proactively identify and assess risks and manage existing risks in line with corporate and cGMP guidelines

We appreciate your application if you have:

University degree aschemist chemical engineer bioengineer pharmacist or specialized teaching diploma
3years of professional experience in pharma/chemical industry -primarily analytical experience especially experience gained in quality control
Maintenance/qualification knowledge and practice related to analytical equipment
Knowledge of validation / qualification documentation
GMP knowledge
User-level computer skills
Intermediate professional English language skill

Should you be interested in this position please let us know by submitting your CV via the advertisement - our colleagues will soon contact you with the details.

Create and continuously update documentation related to the inspection of devices and processes within your area of control
Design validation plans for computer systems used in product quality control tests
Prepare calibration and qualification plans and reports for analytical instruments
Ensure quality assurance perspectives are considered when ordering new equipment and defining user requirements (URS)
Collaborate in the development of procedures and the commissioning of instruments
Follow implement and continually improve data integrity guidelines within quality control
Participate in the development of economic and efficiency indicators characteristic of the area (data provision and analysis)
Continuously monitor the GMP requirements ensure compliance and provide necessary training and updates
Proactively identify and assess risks and manage existing risks in line with corporate and cGMP guidelines

We appreciate your application if you have:

University degree aschemist chemical engineer bioengineer pharmacist or specialized teaching diploma
3years of professional experience in pharma/chemical industry -primarily analytical experience especially experience gained in quality control
Maintenance/qualification knowledge and practice related to analytical equipment
Knowledge of validation / qualification documentation
GMP knowledge
User-level computer skills
Intermediate professional English language skill

Should you be interested in this position please let us know by submitting your CV via the advertisement - our colleagues will soon contact you with the details.