Critères de l'offre

• Métiers :

  • Manufacturing process engineer

• Diplômes :

  • BA (Bachelor of Arts) / BSc (Bachelor of Science)
  • + 1 diplôme

• Compétences :

  • Process
  • Regulatory requirements

• Lieux :

  • Lausanne

• Conditions :

  • Permanent contract
  • Full Time

Critères de l'offre

• Métiers :

  • Manufacturing process engineer

• Diplômes :

  • BA (Bachelor of Arts) / BSc (Bachelor of Science)
  • + 1 diplôme

• Compétences :

  • Process
  • Regulatory requirements

• Lieux :

  • Lausanne

• Conditions :

  • Permanent contract
  • Full Time

L'entreprise : LHH

The Adecco Group Switzerland

Plus d'infos sur LHH

Description du poste

For one of our clients, a global leader in biotechnology based between Geneva and Lausanne, we are looking for a Process Manufacturing Engineer (M/F).

As part of a 9-month project and the launch of a product in the biotechnology market, we are looking for a candidate available immediately (within 1 month maximum). There are possibilities to continue on a permanent contract.

Your Responsibilities:

• Develop and optimize manufacturing processes to improve efficiency, quality, and cost-effectiveness.
• Provide technical support to the production team to troubleshoot and resolve process-related issues.
• Ensure that manufacturing processes comply with regulatory standards (GMP, ISO) and company quality policies.
• Identify opportunities for process improvements and implement changes to enhance productivity and reduce waste.
• Create and maintain detailed documentation of manufacturing processes, including standard operating procedures (SOPs), process flow diagrams, and validation protocols.
• Oversee the installation, qualification, and maintenance of manufacturing equipment to ensure optimal performance.
• Train production staff on new processes and equipment to ensure proper implementation and adherence to procedures.
• Work closely with R&D, quality assurance, and maintenance teams to ensure seamless integration of new processes and technologies.
• Analyze production data to monitor process performance and identify areas for improvement.
• Ensure all processes and documentation meet regulatory requirements and participate in internal and external audits.

Your Profile:

• Bachelor's degree in engineering/ chemical engineering, Biotechnology, or a related field.
• Previous experience in a manufacturing environment, preferably in the biotechnology or pharmaceutical industry.
• Knowledge of bioprocessing techniques, process validation, and regulatory requirements (GMP, ISO). Proficiency in process simulation software and data analysis tools.
• Strong analytical and problem-solving skills to identify and address process inefficiencies.
• Ability to manage multiple projects simultaneously and meet deadlines.
• Behavioral and Soft Skills
• Ability to work effectively in a team-oriented environment and collaborate with cross-functional teams.
• Excellent verbal and written communication skills to convey technical information clearly.
• High level of attention to detail to ensure accuracy and compliance in all processes.
• Ability to adapt to changing priorities and work in a fast-paced environment.
• Proactive approach to identifying and implementing process improvements.
• Available now or within 1 month.

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