Cleaning Validation Scientist/Engineer

Switzerland  ‐ Onsite
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Description

Cleaning Validation Scientist/Engineer

Our client, one of the largest pharmaceutical companies in the world, is currently seeking a Cleaning Validation Scientist/Engineer to be part of their Drug Substance Cleaning Validation Team.
  • contract
  • 6 months
  • Central Switzerland


As a Cleaning Validation Engineer you will be required to generate and execute documentation in relation to the Process and Cleaning Validation programmes including Master Validation Plans, Protocols, and Reports in line with cGMP, EU, FDA and Risk MaPP guidelines. To coordinate the Process and Cleaning Validation programmes in the Laboratories. In addition, to aid and participate in technical investigations in support of the various groups on site in particular the Manufacturing department. Complete document preparation and execution of these activities. Work with Project Manager to develop cleaning validation strategies / grouping documents. Schedule protocol generation & execution to meet indicated due dates. You will work with team members to facilitate protocol preparation, execution, troubleshooting and sample submission/results- including Manufacturing, Engineering, Facilities, QC Chemistry, QC Microbiology.

Requirements:
  • A minimum of three years experience in a similar role.
  • Specific experience in Cleaning Validation (Solid Dosage preferable) is required.
  • Good knowledge of manufacturing processes
  • Knowledge of process validation would be a distinct advantage.
  • Good verbal and written communication skills in English, German desirable
  • Excellent trouble shooting and problem solving skills
  • Good computer skills (MS Word, Excel and PowerPoint)
  • Good attention to detail
  • Ability to think logically and be proactive.
  • Ability to work as part of a team and on own initiative in a constructive manner
  • Flexible and self-motivated

  • Proven track record in cleaning validation in bulk bio industry
  • Experienced in Document preparation and Execution
  • Experience in developing and implementing grouping strategy documents for cleaning studies
  • 3rd level qualification in a science related discipline.


For more information on this or other opportunities, please send me your CV or please contact Sabina Keel at Real Staffing on or

Keywords: Cleanline Validation, Cleanline Engineer, Pharmaceutical, Sterile,
Start date
07/0001
Duration
6 months
From
Real Staffing
Published at
25.06.2015
Project ID:
931661
Contract type
Freelance
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