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Production Supervisor
2 months ago
Job Summary
The Production Supervisor plays a critical role in ensuring the efficient and effective operation of Baxter's manufacturing facilities. This position is responsible for coordinating the final inspection and packing of the Viaflex product using highly sophisticated automated equipment.
Key Responsibilities
- Coordinate the final inspection and packing of the Viaflex product using automated equipment.
- Monitor the activities of team members and machinery to ensure quality standards and specifications are met.
- Clean and sanitize equipment and facilities to maintain a safe and healthy work environment.
- Utilize Baxter's Shared Commitment framework to lead the team and drive a high-performing culture.
- Responsible for Overpouch operations in addition to Afternoon & Midnight Shift Supervision.
Essential Duties and Responsibilities
- Set up, adjust, troubleshoot, and maintain automated equipment to ensure optimal performance.
- Provide technical support to employees to resolve quality and equipment issues.
- Schedule daily activities to ensure a constant supply of empty sterilizer trucks to the filling department while maximizing departmental efficiencies.
- Improve team effectiveness by providing documented training, coaching employees during feedback reviews, and daily activities to improve skills.
- Identify and implement Value Improvement Projects to reduce product cost or improve quality by monitoring scrap and efficiencies.
- Ensure all activities and products are in compliance with specifications and GMPs by reviewing batch records and taking corrective actions as needed.
- Maintain the facility and equipment to meet all GMP and 6S requirements.
- Meet financial commitments by ensuring budgeted labor standards are met and assisting in establishing budget, production standards, and manufacturing expenses for the department.
Requirements
- High School diploma or equivalent required; post-secondary education preferred.
- Experience within a manufacturing operation, preferably in a pharmaceutical manufacturing environment.
- Strong mechanical aptitude and equipment trouble-shooting ability.
- Practical experience using Lean tools, such as 6S, LSW, VM, DA, Kaizen, and Value Stream Mapping.
- Knowledge of GMP, ISO standards, and regulatory/corporate requirements.
- Previous supervisory experience in a GMP regulated manufacturing facility.
- People management experience, including coaching and team development skills.
- Strong communication skills and ability to work with all levels of the organization.
- Ability to balance multiple priorities in a fast-paced, high-pressure environment.
- Self-motivated with a strong ability to take a leading role in the continuous improvement cycle.
- Strong analytical and problem-solving skills, with critical thinking abilities.
- Intermediate proficiency in Microsoft Office, including Word, Excel, and PowerPoint, as well as EBR and AS400/Kronos.
- Good working knowledge of SOPs/specs, blueprints, PCSs, and BOMs.
- Carton Forming equipment, case sealer, Pack line Robot(s) knowledge.
- Afternoon/Midnights – Overpouch, Altairs, Amplass, PPB Fill and Pack equipment knowledge.
