For our international pharma client we are looking for a
Project Engineer (m/f/d).
Duration: 12 months (extension possible)
Location: Visp
Workload: 100%
5 days per week onsite
Key Duties & Responsibilities:
* Direct, coordinate, and lead planning, organization, control, integration, and completion of engineering projects within assigned responsibility
* Plan and formulate engineering programs; organize project staff according to project requirements
* Assign project personnel to specific phases or aspects of projects (technical studies, product design, preparation of specifications and technical plans, product testing) in line with engineering disciplines
* Ensure compliance with GMP and ISO standards throughout project lifecycle
* Oversee qualification and validation activities (Quali/Vali), including GC/IQ phases and documentation
* Manage facility design projects, including production lines, warehousing, fill & finish lines, and clean rooms
* Collaborate with cross-functional teams in a varied group environment to deliver projects on time and within scope
* Drive engineering compliance and CQV (Commissioning, Qualification, and Validation) processes for pharmaceutical manufacturing facilities
Experience and Qualification:
* Degree in Engineering or related field
* Previous roles such as Process Engineer, Qualification Engineer, or Compliance Engineer.
* Minimum 10 years in pharmaceutical engineering/manufacturing
* Technical Expertise must include GMP compliance and ISO standards
* Qualification and validation (Quali/Vali), including GC/IQ phases
* Experience in any of the following: Facility design, clean room projects, fill & finish lines, production lines, warehousing, etc.
* ENC/CQV processes
* Project Management qualification would be nice to have
* Must have pharmaceutical and manufacturing
* Fluent in German (mandatory)