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.