In this role, you will lead and coordinate technical investment projects within a GMP-regulated biopharmaceutical manufacturing environment. You will act as a key interface between engineering, operations, and quality teams to ensure the successful implementation of mechanical modifications and process improvements. The position combines technical expertise, operational support, and project execution in a highly regulated production setting.

Start Date: ASAP

Duration: approx. 6 Months

Place of Work: Visp

Key Responsibilities

  • Define project requirements, timelines, and technical objectives in alignment with operational and compliance standards
  • Support the development and execution of capital investment projects from design phase through qualification activities
  • Serve as the main technical contact for mechanical modifications and process optimization initiatives
  • Coordinate closely with production, engineering, maintenance, and quality departments to ensure smooth project execution
  • Ensure all activities are performed according to GMP requirements and internal quality procedures
  • Support change control activities including preparation and review of technical documentation and change records
  • Monitor project progress, budget, timelines, and key deliverables
  • Identify project risks and implement mitigation strategies to minimize operational impact
  • Provide technical guidance and hands-on support during implementation and operational improvement activities
  • Lead commissioning and qualification activities including IQ, OQ, and PQ phases
  • Collaborate with validation teams to ensure systems and processes meet operational and compliance expectations
  • Prepare technical reports, project updates, and stakeholder presentations

 

Candidate Profile

 

  • Bachelor’s or Master’s degree in Engineering, Life Sciences, Biotechnology, or a related technical discipline

  • Several years of experience within biopharmaceutical or GMP-regulated manufacturing environments

  • Strong background in technical project management, operational excellence, or engineering projects

  • Hands-on experience with commissioning, qualification, and validation activities within GMP operations

  • Solid understanding of GMP regulations, change management, and quality standards

  • Experience coordinating cross-functional teams and external partners

  • Strong organizational and problem-solving skills with the ability to manage multiple priorities simultaneously

  • Excellent communication skills and stakeholder management capabilities

  • Structured, detail-oriented, and proactive working style

  • Fluent German language skills are highly preferred

  • Professional English skills are required

     

Job ID 19041