Beschreibung
The primary objective of this role is to ensure the correct application of Technical Standards and engineering principles throughout various project phases. This involves close collaboration with the technical team from design to commissioning, as well as the sharing of technical standards and auditing for compliance. Strong technical knowledge is essential for tasks such as reviewing P&IDs.Responsibilities:
* Communicate and enforce relevant standards and practices with the project team and Work Package Owners.
* Proactively align and maintain alignment with various Lonza Project Team members and stakeholders regarding technical standards.
* Participate in technical meetings between Work Package Owners and suppliers. * Review and approve technical documentation, including P&IDs.
* Coordinate declaration of conformity according to PED.
* Organize internal and external workshops and assist team members in establishing agendas, meeting minutes, and action lists.
* Assist in project reporting preparation, including KPI charts and information collection.
* Participate in approval workflows in Unifier and CQV.
* Participate in FATs / SATs as an observing auditor.
* Lead discussions on technical change management, determining whether proposed changes are mandatory or optional, and coordinate Technical Change Requests (TCRs) in SAP.
* Prepare for the handover of technical information from EPCMQ to Plant Engineering and execute it during the initial handover.
Candidate profile:
- Education: Bachelor or Master degree in Engineering (process, pharmaceutical, biochemical or equivalent)
- Experience
- 2+ years in project engineering or project management for (bio)chemical, or pharmaceutical industries with international experience.
- Technical knowledge of the various engineering disciplines in the Pharmaceutical environment, both on clean and black utilities, process, automation, Instrumentation and Civil Engineering
- Task orientated person who is very comfortable working towards set objectives and has a track record of achieving results in this regard.
- Knowledge
- Excellent knowledge of computer systems (i.e. Microsoft Word, Excel, PowerPoint, and Visio).
- Experience at working both independently and in a team-oriented, collaborative environment is essential.
- Skills
- A good memory and organization is required to keep the overview of the technical standards.
- Strong verbal and written communication skills (English and German).
- Effective influencing skills. Ability to communicate to varying levels and functions of the organization.
- Strong collaborative mindset.
- Strong organizational skills, ability to balance multiple priorities simultaneously.
- Can conform to shifting priorities, demands and timelines through analytical and problem-solving capabilities.
- Strong project management skills.
- Experience in Engineering and cGMP Manufacturing
Sthree Switzerland is acting as an Employment Business in relation to this vacancy.