Manufacturing Supervisor (Biopharmaceutical, On-site)

Job summary

This role involves leading daily bioprocess operations in a manufacturing environment, ensuring production runs efficiently while adhering to safety, quality, and compliance standards. The supervisor will work closely with operators and technicians, directly impacting production performance and the delivery of biologic medicines.

Qualifications

• Experience in biopharmaceutical or GMP-regulated manufacturing
• Bachelor’s degree in biotechnology, chemical engineering, life sciences, or equivalent practical experience
• 4–6 years of experience in production environments with team leadership or coordination responsibilities
• Strong understanding of GMP standards, EHS requirements, and manufacturing documentation
• Basic knowledge of Upstream processes and equipment
• Experience in shift-based production, Lean principles, or continuous improvement is advantageous

Responsibilities

• Oversee manufacturing activities on assigned shifts, ensuring alignment with approved procedures and regulatory requirements
• Coordinate daily tasks and monitor process performance
• Resolve operational challenges in real time
• Facilitate communication across shifts
• Collaborate with Quality, Engineering, and Supply Chain teams to maintain smooth operations
• Contribute to deviation handling, investigations, and continuous improvement initiatives
• Support onboarding, training, and qualification of employees
• Conduct performance conversations and provide constructive feedback

Skills

• Strong leadership presence and ability to guide teams
• Clear communication skills and composure under pressure
• Problem-solving ownership alongside team members

Education

• Bachelor’s degree in a relevant field or equivalent practical experience

Tools

• Familiarity with manufacturing documentation and GMP compliance tools