Project Manager Capital Engineering (m/f/d)
Mehr als 30 Tage altAngaben zum Job
| Firma | Aristo Group Personalvermittler |
| Kategorie | Ingenieurswesen | Pensum | 100% |
| Lohn (geschätzt) | CHF 88'000 – 112'000 / Jahr |
| Einsatzort | Boudry |
Job-Inhalt
Skills: Solid Dosage,Design,CAPEX (Engineering)
Start of project: 18.12.2023
Duration of the project : 8 Months
Project volume: 1344 Hour(s)
Location: Boudry, Schweiz
Tasks:
- Responsible for preliminary designs for manufacturing process equipments, including P&ID development and HAZOP facilitation.
- Selection and review of suppliers.
- Responsible to review and approve design, PFD preparation, equipments and utilities sizing.
- Provides technical guidance during project implementation, assures viability of technology in proposed configuration, adherence to company standards and practices.
- Share best practices and promote harmonization while optimizing cost.
- Establish engineering standards and keep content current and compliant through periodic review and successful integration with third party designers/integrators.
- Management of external engineering contractors and companies working on site.
- Successfully interface with manufacturing team, maintenance team, project managers and engineering professionals.
- Lead project execution, equipments installation including commissioning, Factory Acceptance Test (FAT) and Site Acceptance Test (SAT).
- Manages investment projects, participate to the investment strategy and budget definitions.
- Coordinates different teams as Project Manager working on new projects.
- Leads or supports commissioning and qualification activities.
- Participates to the selection of new contractors.
- Support troubleshooting of existing pharmaceutical equipment.
- Perform Technology Survey in his areas of expertise.
- Promotes a company culture centred around Health & Safety to all employees and encourages them to maintain a safe and secure work environment at all times.
- EHS
Qualifications:
- 3-5 years experience in a pharmaceutical company or other related industry.
- Good knowledge of GMP and FDA regulatory requirements.
- Good technical knowledge and experience in project management.
- Good knowledge in process technologies (solid dosage forms, packaging…)
- Good knowledge in technical infrastructures (HVAC, utilities...)
- Good knowledge in the validation of procedures and systems.
- Good knowledge of risk analysis tools required
- Fluent in English and French.
- Excellent written and communication skills.
- Excellent organizational skills.
- Excellent team spirit.
- Ability to take decision.