Production Quality Expert (m/w/d) - Pharma at AqVida GmbH
berlin, Berlin, Germany -
Full Time


Start Date

Immediate

Expiry Date

21 Dec, 26

Salary

90000.0

Posted On

22 Sep, 26

Experience

4 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Pharmaceutical Manufacturing

Description

Your tasks include:

  • End-to-end project management for production facilities, from procurement and installation to qualification and transition to qualified routine operation.
  • Coordination, creation and revision of GMP documents (e.g. batch records, deviations, CAPAs, change control, logbooks, training and SOPs)
  • Support for routine processes (technology, warehousing, inspection, packaging and cleanroom)
  • Continuous improvement of systems to meet the latest standards and GMP requirements.
  • Support in complying with pharmaceutical regulations, manufacturing regulations, GMP guidelines, safety and environmental regulations in the production area (within the meaning of §22 AMWHV)

Your profile:

  • Completed studies in the field of chemistry, pharmacy, pharmaceutical technology, mechanical engineering or a comparable field.
  • Professional experience in a manufacturing company, preferably in the pharmaceutical or food industry
  • Very confident command of the German and English languages, both spoken and written.
  • Proficient use of common Office applications (Word, Excel, Outlook)
  • An open, independent, and communicative personality who approaches and motivates other people.
  • You possess excellent problem-solving skills and very good practical judgment, and you work in a structured, responsible, and timely manner.


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Responsibilities

Your tasks include:

  • End-to-end project management for production facilities, from procurement and installation to qualification and transition to qualified routine operation.
  • Coordination, creation and revision of GMP documents (e.g. batch records, deviations, CAPAs, change control, logbooks, training and SOPs)
  • Support for routine processes (technology, warehousing, inspection, packaging and cleanroom)
  • Continuous improvement of systems to meet the latest standards and GMP requirements.
  • Support in complying with pharmaceutical regulations, manufacturing regulations, GMP guidelines, safety and environmental regulations in the production area (within the meaning of §22 AMWHV)

Your profile:

  • Completed studies in the field of chemistry, pharmacy, pharmaceutical technology, mechanical engineering or a comparable field.
  • Professional experience in a manufacturing company, preferably in the pharmaceutical or food industry
  • Very confident command of the German and English languages, both spoken and written.
  • Proficient use of common Office applications (Word, Excel, Outlook)
  • An open, independent, and communicative personality who approaches and motivates other people.
  • You possess excellent problem-solving skills and very good practical judgment, and you work in a structured, responsible, and timely manner.


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