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 c GMP compliance and safety protocols. Your leadership will be instrumental in driving operational excellence and ensuring the quality and efficiency of our manufacturing processes. Principal Accountabilities:
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 c GMP regulations and biotech 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!