Requirements: English
Company: WhatJobs
Region: switzerland, schweiz ,
Our client is a global biopharmaceutical company located near Neuchatel, Switzerland.
Focused on R&D and delivery of innovative medicines across several therapeutic areas, including oncology, hematology, immunology, and CVD.
The Role
This position is responsible for managing engineering projects regarding the implementation of equipment and process systems in GMP Facilities. The candidate will ensure the development and review of engineering guidelines and standards for GMP utilities and OSD process technology.
Responsibilities
- Responsible for preliminary designs for manufacturing process equipment, including P&ID development and HAZOP facilitation.
- Selection and review of suppliers.
- Review and approve design, PFD preparation, equipment, and utilities sizing.
- Provide technical guidance during project implementation, ensuring viability of the technology and adherence to company standards.
- Share best practices and promote harmonization while optimizing costs.
- Establish and keep engineering standards current and compliant through periodic reviews and integration with third-party designers/integrators.
- Manage external engineering contractors and companies working on site.
- Interface effectively with manufacturing, maintenance teams, project managers, and engineering professionals.
- Lead project execution, including equipment installation, commissioning, FAT, and SAT.
- Manage investment projects and participate in strategy and budget planning.
- Coordinate teams as Project Manager on new projects.
- Support commissioning and qualification activities.
- Participate in selecting new contractors.
- Assist in troubleshooting existing pharmaceutical equipment.
- Perform technology surveys in areas of expertise.
- Promote a safety culture and ensure a safe work environment.
EHS
Line managers shall provide a safe and healthy work environment, ensuring compliance with relevant rules and legislation.
Work closely with EHS to evaluate hazards and perform risk analyses.
Ensure staff is informed and trained on hazards and safety procedures.
Promote safe practices, verify rule compliance, and report incidents and near-misses.
Participate in investigations and implement preventive measures.
You
Our client seeks someone with:
- 3-5 years of experience in a pharmaceutical or related industry.
- Good knowledge of GMP and FDA regulatory requirements.
- Strong technical and project management skills.
- Knowledge of process technologies (solid dosage forms, packaging, etc.).
- Understanding of technical infrastructures (HVAC, utilities, etc.).
- Experience with validation of procedures and systems.
- Familiarity with risk analysis tools.
- Fluency in English and French.
- Excellent written and communication skills.
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