QC Instrument Expert Global Pharma Manufacturing Site Pest County
Posted on :
04-07-2024
Employer Active
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Share
Send me jobs like this
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Job Description
Supporting a special field we are looking for an ambitious and broadminded person on behalf of our global partner who manufactures solid pharmaceutical products in Hungary. In this position you will be the taskmaster of the site's 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. Daytoday work requires close cooperation with internal and external departments such as supplier companies or QC Managers.
Your key responsibilities:
For investment projects you play a determinative role in the procurement process of the new machine park and the support during the installation period. Daytoday 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 as chemist chemical engineer bioengineer pharmacist or specialized teaching diploma
- 3 years 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
- Userlevel 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.
Employment Type
Full Time
Key Skills
Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.
