• Contract
  • Valais
  • Recruiter: TargetRecruit Admin

Providing Flexible Resourcing Solutions

Founded in 1997 and headquartered in Basel, Switzerland, CTC is a specialist life-sciences recruitment organisation. We place specialist talent into contract and permanent positions in the pharmaceutical, biotech, medical devices and CRO industries.

 

Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a

 

CQV Lead USP or DSP

 

LONCAP_240214_PB1

 

Our client is a leading pharmaceutical company focused on biopharmaceuticals, is currently recruiting for a CQV Lead UPS or DSP to be responsible for the preparation and the execution of the CQV activities relating to Upstream or Downstream Process Equipment.

 

 

This role is an initial 12 months contract with extension, to be based in Visp, Switzerland.

 

 

Main Responsibilities:

  • Self-manage CQ development and execution activities with respect to the relevant systems.
  • Function as a key member of the CQ Team, and provide guidance regarding Upstream Process Equipment
  • Maintain control over the activities and schedule with respect to the relevant systems.
  • Participate in sessions to define/agree work breakdown structure with respect to the relevant systems
  • Assist in assessing project risk and evaluating the effectiveness of mitigation strategies applied.
  • Coordination and communication with other resources for Upstream Systems-related matters.
  • Adherence to project procedures/requirements with respect to Health/Safety/Environmental, Quality (including GDP/GMP), CQ (including MCP, MQP, DQ, IQ, OQ, Commissioning).
  • Liaise closely with the relevant vendors/providers/contractors, project Automation representatives and Construction-phase representatives to ensure integration of activities and schedules with respect to the relevant systems.
  • Actively participate in the development and delivery of deliverables with respect to the relevant systems.
  • Report on key deliverable and dates and align with key milestones within the project’s critical path.
  • Report and aid in the resolution of project issues, including maintaining the non-conformance records.
  • Assist in assessing project risk and evaluating the effectiveness of mitigation strategies applied.
  • Prioritize and execute tasks in a fast-paced environment.

   

Qualifications and Experience:

  • Relevant working/residency permit or Swiss/EU-Citizenship required
  • Minimum Bachelor’s degree in Life Sciences or Engineering
  • Minimum of 6+ years of experience in commissioning / qualification / validation (DQ, IQ, OQ, Commissioning) activities in the pharmaceutical/biotech industry.
  • Proven Upstream / Dowstream system and CIP / SIP knowledge.
  • Minimum 6+ years of experience in commissioning / qualification / validation of Downstream systems.
  • Experience with DeltaV (Emerson).
  • Fluent English language written and verbal communication skills
  • Fluent German is a distinct preference
  • cGMP knowledge and knowledge of regulatory requirements.
  • Able to work with minimum oversight fulfilling deliverables within target dates.
  • Experience with Lonza Commissioning / Qualification Approach.
  • Experience with COMOS/KNEAT platforms.

 

Would you like to learn more about CTC and the opportunity outlined? Please, get in contact with us: you may either use the 'apply now' button, or write an email to us, or reach out to us on the phone.

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