Updated: Aug 19, 2024
The Company
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 related to the implementation of equipment and process systems in GMP Facilities. The successful 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 technology and adherence to company standards.
Share best practices and promote harmonization while optimizing costs.
Establish and maintain engineering standards, ensuring content is 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, project management, and engineering teams.
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.
Assist in selecting new contractors.
Support troubleshooting of existing pharmaceutical equipment.
Perform technology surveys in relevant areas.
Promote a culture of health and safety, ensuring a safe work environment.
Collaborate with EHS to evaluate hazards, perform risk analyses, and ensure safety training and compliance.
You
Our client is seeking candidates 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.
Proficiency in risk analysis tools.
Fluency in English and French.
Excellent communication, organizational, and team skills.
Decision-making abilities.
Note
This position has been filled. Please contact recruitment@consultantsinscience.com to be informed of future similar positions.
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