Downstream Purification & Filtration Specialist

Location
Poland
Salary
On Application
Posted
19 Nov 2018
Closes
19 Dec 2018
Ref
CWi
Discipline
Quality, QA / QC
Contract Type
Contract

Role and Responsibilities:

  • Carry-out and monitoring of biotechnological production processes according to technological documentation, GMP rules and internal quality requirements
  • Analysis of achieved process data according to compliance with technological documentation and internal requirements
  • Participation in technology transfer and process validation in cooperation with Research and Development Department
  • Preparation of documentation according to GMP rules and company internal requirements
  • Preparation of Standard Operational Procedures and instructions and trainings for its implementation
  • Ensuring effective production activities preparation and carry out, responsibility for production process continuity, reporting of performed actions statuses
  • Supervision of proper raw materials expenditure during technology transfer and production processes
  • Shift work

Required Qualifications:

  • Higher education (at least Bachelor) in biotechnology, pharmacy or similar
  • Minimum two year experience in biotechnological or pharmaceutical industry
  • Good knowledge of cGMP requirements
  • Good work organization and individual problem solving skills
  • Chromatography technics as affinity chromatography and ion exchange chromatography (CEX and AEX)
  • Good communication, team cooperation skills and being open for new tasks
  • Very good command of English, both written and spoken 

Additional Assets:

  • Experience in keeping records of production documentation according to GMP requirements
  • Knowledge of filtration techniques (like tangential flow filtration - TFF) and aseptic techniques
  • Experience in work with recombinant proteins
  • Experience in single use materials usage for biopharmaceutical production

 

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