Beschreibung
Process Engineer Solid Handling (m/f)Start: as soon as possible
Location: Canton Bern
Duration: 6 months
Remote: no
For one of my big Greenfield pharmaceutical clients I am looking for a Process Engineer (m/f).
Main responsibilities:
- The position holder acts as process engineer for the solid handling system
- He is responsible for reviewing and approving the technical specifications from the supplier and for coordinating with all internal and external points of contacts concerning this system. In addition the position holder will provide technical support for the installation, commissioning and qualification of the solid handling system
- The position holder reports to the Project Engineering Manager.
- The position holder is responsible for the on time delivery of the engineering documents (technical specifications) of the solid handling system.
- The position holder coordinates project activities within the organization as well as with external suppliers.
- The position holder is responsible that the requirements from production regarding processes are the base for the engineering of the equipment, layout, and rooms through Detailed Design, Construction, Commissioning, Qualification and Start Up within the building
- Coordinating/aligning closely with manufacturing personnel as well as plant engineering and services.
Key Interfaces
- Manager Warehouse and Logistics
- Manager Manufacturing Support (Dispensing)
- Project Engineer Media and Buffer Equipment
- Manager Qualification
- Plant Engineering and Services
Technical Responsibilities
- Review and approve engineering documents such as RS, Layouts, 3D Models, PID's and Functional Specifications
- Coordinate, schedule and control all design activities within his area and other stakeholders (Engineering, Manufacturing, ICQ, QM-Val & BOS). This also includes facilitation for problem solving and preparing technical solutions.
- Hand over and actively support construction third parties and ICQ to ensure that the mechanical completion, commissioning and IQ/OQ/PQ steps are achieved in line with the master schedule and support the startup of the equipment
- Coordinate and communicate with the external partners and suppliers to ensure overall coordination of the design, timelines and resources.
- Coordinate, schedule and control all design activities within his area and other stakeholders (Engineering, Manufacturing, ICQ, QM-Val & BOS). This also includes facilitation for problem solving and preparing technical solutions.
- Hand over and actively support construction third parties and ICQ to ensure that the mechanical completion, commissioning and IQ/OQ/PQ steps are achieved in line with the master schedule and support the startup of the equipment
- Ensure that the Facility design intent is reflected within quality driven design deliverables and in accordance with the Project Brief, User Requirements, Local Authority and Global Regulatory requirements as well as industry best practices.
- Is actively involved in / contributes actively to issue resolution, assisting cross-functional teams and attending coordination meetings between the various engineering disciplines leads to ensure smooth installation, construction and commissioning of the facility.
- Bears responsibility and accountability for working according to cGxP, health, safety and environmental requirements as laid out in the SOPs and procedures as well as all relevant external / governmental guidance.
- Contributes to the delivery of the company strategy as well as supports the financial CapEx budgeting process for the engineering and Project Management Organization.
Education:
- Degree (Bachelor, Masters or higher) in process, mechanical or chemical engineering, Dipl. lng. or M.Sc. or B.Sc. or equivalent
- Languages: English and German fluent in writing and spoken (B2)
Experience:
- Proven experience and knowledge in pharmaceutical plant engineering and construction.
- Several years (>5 years) of successful process technology support and leadership experience on mid-sized and major projects with high complexity in the chemical, biotech-or pharmaceutical industry.
- Project experience gained within the design, procurement, construction & qualification environment of a pharmaceutical plant
- Proven experience in cGMP & GDP and qualification.
Competencies:
- Technical expertise in pharmaceutical process engineering and logistics.
- Technical Project Management skills including priority setting, organizing and timely decision making
- Approachable Team player with advanced communication skills
- Proactive and solution oriented
If you are interested in this position please send me your updated CV to or give me a call on .
Looking forward to speaking to you
Kaja
Sthree Switzerland is acting as an Employment Business in relation to this vacancy.