Supervisor II, Production (Morning Shift)

Confluent Medical Technologies is a financially healthy and rapidly growing medical device company dedicated to working collaboratively with our customers, taking their projects from rapid prototype into high volume production. Our unparalleled technical expertise, proven experience and partnership with our clients has allowed us to perfect the process necessary to deliver world-class medical devices through innovative material science, engineering, and manufacturing. Our primary capabilities include: Nitinol components and tubing, balloon expandable stents and catheters, complex catheters, biomedical textiles, and high precision polymer tubing. We take pride in our position as the leader in the medical technology space and are driven by a passion to create products that our clients have envisioned for their customers.

At Confluent, we are committed to our values of teamwork, innovation, accountability, integrity, leadership, and customer focus, and we invest in a team who represents these values. Every member of our team plays a critical role in delivering life-saving medical devices through innovative materials science, engineering, and manufacturing. We are the medical device industry's most trusted partner, and we accomplish this with an organization focused on safety, efficiency, and customer satisfaction.

We are looking for a Supervisor II, Production (Morning Shift) to join our team. If you enjoy working in a fast-paced environment and making an impact on our life-saving work, this may be a good fit for you!

Summary:

Responsible for supervising production operations, ensuring compliance with company policies, labor laws, and quality, health, and safety regulations. Manages workflow, personnel, and production efficiency while driving continuous improvement.

Key Responsibilities:

Oversee daily production activities, training, and performance reviews.

Interview, hire, discipline, and resolve employee issues.

Ensure compliance with company guidelines, quality systems, and safety standards.

Plan, schedule, and monitor production to meet goals and report results.

Lead process improvements and corrective actions (Lean, Six Sigma).

Maintain a safe, clean, and efficient work environment.

Supervises: Production Associates I–III, Manufacturing Leads, and Production Clerks.

Requirements:

Bachelor’s in business, engineering, or related field (2+ years in medical industry) OR high school diploma with 6+ years’ related experience.

Strong PC and process improvement skills (e.g., Six Sigma).

Knowledge of labor law, production planning, quality control (CFM, JIT).

Strong leadership, problem-solving, and communication skills.

English (B1/B2) preferred.

This position is an outline of the major recurring responsibilities of the job. It is not intended to be all-inclusive of the work to be performed. The incumbents(s) will typically perform other related job objectives, special assignments and less significant responsibilities.

R-105732