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Engineer - Biotechnology (m / f / d)

Engineer - Biotechnology (m / f / d)

GULP – experts unitedPenzberg
Vor 30+ Tagen
Stellenbeschreibung

Time for change - time for a new job! Are you a scientist looking for a new professional challenge in the field of ITOT Compliance in Penzberg ? Randstad Professional has what you are looking for : A secure job, attractive benefits and a job with exciting tasks in the pharmaceutical sector .

Here's what we offer

  • Attractive salary and long-term job security through group affiliation
  • Up to 30 days vacation per year
  • Contribution to company pension scheme after end of probationary period
  • Extensive social benefits, including Christmas and vacation bonuses
  • Reimbursement of travel expenses
  • Generally an open-ended employment contract
  • Good chances of being taken on by our business partners
  • Tailored further training opportunities and free language courses
  • A wide range of employee benefits

Your tasks

  • Creation, processing, follow-up and closure of changes, deviations, corrections and preventive measures
  • Performing quality assurance tasks for the unit's QA, IT and automation systems, including associated processes (e.g. archiving, maintenance of master data and maintenance contracts, data integrity)
  • Creation and processing of risk analyses in the quality risk management environment
  • Ensuring operational GMP-relevant documentation (e.g. records management) or the creation and processing of regulations (e.g. content management) in the automation environment
  • Preparation, support and follow-up of audits and inspections
  • Representation of the unit with regard to QA and training topics, as well as the implementation and organization of training courses in the unit
  • Supporting validation and qualification projects and participating in the establishment of new IT & automation systems
  • Your profile

  • Bachelor, Master, Diploma, e.g. chemical engineer, biotechnology engineer, university degree in the field of computer science, chemistry, biology, biotechnology, process engineering or an equivalent technical education with experience from practical activities
  • 4-6 years of professional experience after graduation (no graduates without non-university professional experience, internships or similar during the course of studies do not count)
  • Experience in quality assurance
  • Experience in the GMP environment is an advantage
  • Experience as a (partial) project manager or in-depth knowledge of automation technology or complex IT systems
  • Knowledge of pharmaceutical manufacturing and software development processes
  • Specialized knowledge and limited management tasks or responsibility for sub-areas, ongoing activities, targets and product portfolios
  • Meticulous way of working
  • Fluent German and good English skills