Oversight Quality Engineer Global Pharma Manufacturing Site Budapest

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profile Job Location:

Budapest - Hungary

profile Monthly Salary: Not Disclosed
Posted on: 21 hours ago
Vacancies: 1 Vacancy

Job Summary

Due to the expansion of our global pharmaceutical manufacturer partner we are looking for an Oversight QA Associate to join their growing team in job below provides an exceptionally high earning potential in an expanding organizational department with allocated cumulated working time it is possible to get to know new technologies through CDMO projects.

Within a global scale the company is a TOP 3 chemical product developer and manufacturer producing more than 80 APIs in 5 European countries. As an Oversight Quality Engineer you will overview the operation of the existing GMP environment and give input how to improve the flagship sites QA system and performance.

Main responsibilities include:
  • Promoting and supporting continuous quality improvement at plant level: assisting the plant in a corrective and proactive manner making recommendations regarding GMP principles and good documentation practices
  • Overviews that the pharmaceutical principles and site procedures are correctly known understood and applied by all persons involved in API manufacturing.
  • Participates in or leads investigations related to production activities following deviations and complaints
  • Supports monitors and controls the effective implementation of related action plans (CAPAs)
  • Participates in periodic quality review of GMP documentation

Requirements to fulfill the role:

  • Minimum of 2 years of experience in a GMP environment quality assurance quality control or manufacturing
  • Good knowledge of GMP principles
  • Intermediate knowledge of English and proficiency in Hungarian
  • University degree (BSC chemist chemical engineer)
  • User-level computer knowledge
  • Ability to report accurately and to the point
  • Striving for change
Are you interested Do not hesitate to submit your CV andwe would be happy to contact you to share the further details or call Gergely Kosznovszki onphone number.

Required Experience:

IC

Due to the expansion of our global pharmaceutical manufacturer partner we are looking for an Oversight QA Associate to join their growing team in job below provides an exceptionally high earning potential in an expanding organizational department with allocated cumulated working time it is possible...
Due to the expansion of our global pharmaceutical manufacturer partner we are looking for an Oversight QA Associate to join their growing team in job below provides an exceptionally high earning potential in an expanding organizational department with allocated cumulated working time it is possible to get to know new technologies through CDMO projects.

Within a global scale the company is a TOP 3 chemical product developer and manufacturer producing more than 80 APIs in 5 European countries. As an Oversight Quality Engineer you will overview the operation of the existing GMP environment and give input how to improve the flagship sites QA system and performance.

Main responsibilities include:
  • Promoting and supporting continuous quality improvement at plant level: assisting the plant in a corrective and proactive manner making recommendations regarding GMP principles and good documentation practices
  • Overviews that the pharmaceutical principles and site procedures are correctly known understood and applied by all persons involved in API manufacturing.
  • Participates in or leads investigations related to production activities following deviations and complaints
  • Supports monitors and controls the effective implementation of related action plans (CAPAs)
  • Participates in periodic quality review of GMP documentation

Requirements to fulfill the role:

  • Minimum of 2 years of experience in a GMP environment quality assurance quality control or manufacturing
  • Good knowledge of GMP principles
  • Intermediate knowledge of English and proficiency in Hungarian
  • University degree (BSC chemist chemical engineer)
  • User-level computer knowledge
  • Ability to report accurately and to the point
  • Striving for change
Are you interested Do not hesitate to submit your CV andwe would be happy to contact you to share the further details or call Gergely Kosznovszki onphone number.

Required Experience:

IC

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Key Skills

  • Lean Manufacturing
  • Six Sigma
  • CNC Programming
  • Lean
  • Machining
  • Tooling
  • CAD
  • CNC
  • Assembly Experience
  • SolidWorks
  • Kaizen
  • Manufacturing

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