CQ Manager


Basel
Contract
Negotiable
Quality
CR/546342_1748858007
CQ Manager

We have a current opportunity for a CQ Manager on a contract basis. The position will be based in Basel. For further information about this position please apply.

Key Responsibilities:

  • Filling and semi-stoppering (filling, dose control, closing (stoppering), sampling and rejection of vials) using Peristaltic and Piston pump dosing systems for Lyophilized vials.
  • Filling Isolator (Internal environment Grade A (Iso 5), HVAC system, H2O2 decontamination process and Glove integrity tester, Rapid transfer ports for transfer of materials).
  • Lyophilizers with mass spectrometer and dedicated loading and unloading isolator each.
  • ATEC Stopper treatment station and loading arm into the isolator
  • The tasks pertaining to this area are;
  • Ensure that CQV activities are executed in accordance with the C&Q Plan and supporting Validation Plans.
  • Overall planning and execution of the commissioning activities related to allocated areas or systems.
  • Leading and coordinating the C&Q execution effort supported by C&Q EPC teams, Engineering, Operations, and external vendors and contractors
  • Planning and scheduling the commissioning activities according to the C&Q strategy and supporting Validation Plans.
  • Support the updates of Master C&Q Plan and supporting plans during project execution lifecycle.
  • Support development of C&Q schedule by including the activities relevant for the preparation of commissioning test plans and test specifications
  • Coordinating the planning and scheduling of commissioning activities with the construction interface and with other disciplines (HSE, Automation, Electrical, Instrumentation, Operation and Engineering, etc.)

Key Requirements:

  • Minimum of 10 Years extensive experience in CQ for Fill and Finish and related utilities.
  • Preferably Diploma level degree in Mechanical or Chemical Engineering.
  • Extensive experience with Liquid and Lyophilized vial filling lines.
  • Comprehensive understanding of Pharmaceutical/Bio Science "Contract Manufacturing" business and experienced in cGMP.
  • Experienced in calculating project-related resource needs, time, and costs.
  • Experienced as CQV-Lead and/or Project Manager.
  • Field CQV execution experience.
  • Considerable experience with cGMP
  • Strong interpersonal and communication skills.
  • Good Level in English, written and spoken / German a plus.
  • Experience in use of Kneat for documentation development and execution (not mandatory

For further information about this position, please apply with your CV

*Please note, only those with the right to work in Switzerland can apply!

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