The Production Supervisor oversees activities related to supporting the injectable manufacturing team, ensuring high-quality products are produced for patients. This role supervises and coordinates shift production operations, including staffing, scheduling, and overall planning in the manufacturing environment.
Key Responsibilities:
- Demonstrates strong values of integrity, initiative, reliability, and professionalism.
- Fosters a positive, respectful, and inclusive work environment, free from harassment.
- Achieves production goals in areas such as safety, scheduling, deviation reduction, and employee development, while ensuring strict adherence to quality standards.
- Conducts one-on-one performance evaluations and provides timely feedback to address both opportunities and issues.
- Champions a high-performance culture and ensures a safe workplace for all team members.
- Adheres to the company's Code of Conduct, regulatory requirements, and safety protocols.
- Provides leadership, clear direction, and objectives for team members, ensuring alignment with business goals.
- Conducts interviews and makes hiring decisions for hourly staff.
- Identifies and implements process improvements for greater efficiency and optimization in manufacturing.
- Oversees and approves timekeeping for direct reports.
- Supervises the Process Lead in conducting on-the-job training, including risk assessments and onboarding for new or transferring employees.
- Monitors the progress and qualifications of direct reports, ensuring they are properly trained before assuming their duties.
- Ensures batch records are reviewed promptly and any corrections are handled appropriately.
- Manages inventory transactions in the control system in a timely manner.
- Leads investigations and implements corrective actions to prevent recurring issues, in compliance with the company's quality management system.
- Pre-approves batch record expiration dates based on established procedures before production starts.
- Drives continuous improvement efforts in the department, focusing on operational excellence, team engagement, and productivity.
- Performs additional duties as assigned.
- Weekend Shift
Required:
- Bachelor's degree.
- 3+ years of experience in a regulated manufacturing environment, preferably in GMP settings.
- Strong presentation skills for facilitating team meetings and briefings with leadership.
- Excellent organizational and time management abilities.
- Strong interpersonal and communication skills.
- Self-motivated and able to manage multiple tasks in a dynamic and fast-paced environment.
- In-depth understanding of current Good Manufacturing Practices (cGMP).
- Ability to interpret technical documents like batch records and protocols.
- Proficient in Microsoft Office products, including Outlook, Excel, Word, and PowerPoint.
- Strong analytical skills for problem-solving, troubleshooting, and process improvement.
- Ability to stand for extended periods (up to 8 hours or more).
- Demonstrates excellence in attendance, dependability, and safety practices.
