Supervisor Manufacturing M/W

at  Recrutis

JOB SUMMARY:

Are you ready to play a pivotal role in our mission?
As a Supervisor Manufacturing, you’ll lead a dynamic team of Manufacturing Associates, ensuring the seamless execution of daily operations while upholding the highest standards of cGMP compliance and safety protocols. Your leadership will be instrumental in driving operational excellence and ensuring the quality and efficiency of our manufacturing processes.

MINIMUM EXPERIENCE REQUIREMENTS:

• Minimum 7 years of experience in pharmaceutical processing within biotech or pharmaceutical industries.
• Strong leadership skills and experience managing teams in a manufacturing environment.
• Good understanding of Delta V or Syncade or similar automated systems.
• Understanding of full Biotech process.
• Languages: English B1, German and/or French are assets.
  Ready to take the next step in your career and join a dynamic team dedicated to making a difference? Apply now and be part of our exciting journey at Biogen Solothurn

Minimum Education Requirements:

• Bachelor’s degree in biotech, pharmaceuticals, or related field.
• Solid understanding of cGMP regulations and biotech manufacturing processes

• Directing daily manufacturing activities, overseeing batch execution, and resolving issues to maintain operational efficiency.
• Documentation and Compliance: Coordinating and revising manufacturing documentation to ensure compliance with regulatory standards.
• Team Development: Hiring, training, and developing a high-performing team, fostering a culture of collaboration and continuous improvement.
• Training and Validation: Providing comprehensive training on process activities and overseeing validation activities to ensure regulatory compliance.
• Cross-Functional Collaboration: Collaborating with other departments and sites to coordinate manufacturing activities and drive operational success.

Minimum Education Requirements:

• Bachelor’s degree in biotech, pharmaceuticals, or related field.
• Solid understanding of cGMP regulations and biotech manufacturing processes.