Supervisor I, Production
CONFLUENT MEDICAL TECHNOLOGIES INC.

Salary Range:
$72,000.00 - $120,000.00Job Description:
Confluent Medical Technologies is 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, balloon expandable stents and balloon catheters, delivery systems, biomedical textiles, access kits, and guidewires. 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.
We are looking for a Supervisor I, Production to join our team. As a uniquely qualified candidate, you will be responsible for production planning and inventory control for multiple products while prioritizing operations to ensure maximum performance and minimum delay. This individual will take a lead role in continuous improvement, product flow and capacity improvement to improve the overall efficiency of manufacturing while service level targets.
As a uniquely qualified candidate, you will:
Create new productivity tools (e.g. training programs) to increase output quality and assist with CIP projects.
Drive all daily tactical actions to ensure weekly commits are met.
Work closely with planning and purchasing to communicate manufacturing/staffing resources available for projects and any non-conforming/out of stock materials issues arising.
Monitor production schedules and other requirements to assure personnel with proper training and resources are available and priorities have been established correctly.
Oversee all action of lead involvement to problem projects (i.e. Week in Review)
Effectively communicates with management, peers and staff.
Responsible performance appraisals and disciplinary action as required.
Attend meetings to contribute and communicate information Know company policies and procedures and assist as needed in the communication and upholding.
Promote a positive and safe work climate.
Must be able to articulate verbally and in writing reports, directions and problems and solutions.
Conduct internal audits, expedites production output and control workflow.
Ensure manufacturing staff is completing work that meets and/or exceeds customer quality specifications and timelines.
Advise Manufacturing Manager of staffing needs for group and assist in applicant screening, testing, and final selection.
Oversees all training and management of Operators and Leads.
Responsible for coaching and developing employees and resolving staff issues.
Responsible for all production activates and staff and is accountable for the efficient use of time and quality.
Utilize computer-based tracking, reporting and material planning and other management tools to effectively monitor and report on key performance objectives.
Education & Experience:BS preferred, AS OR over five years in the technical disciplines and must have direct application of management techniquesISO 13485 and GMP experience; internal audit training preferred
Develop staff by providing effective training.
Drives all aspects of a safe and healthy work environment.
Lead and work with staff and resolve operational problems on all products and processes.
Lead and encourage all staff members to think forward and anticipate problematic areas of a project and use problem solving skills to accurately define and resolve root cause issues.
Take a leadership role in problems or critical issues that may prevent the success of the company.
Able to work independently (without direct supervision) 100% on all tactical activities of the department
Able to motivate others and drive results
Flexible and have strong aptitude for planning and prioritizingComputer proficient and able to read and interpret engineering designs
We regret that we are unable to sponsor employment visas or consider individuals on time-limited visa status for this position.
OTHER SKILLS and ABILITIES: Ability to use PCs, and associated software, including databases. General knowledge of GMPs. Ability to work with associates at all levels of the organization. Good written and oral English communication skills.
How to apply
To apply for this job you need to authorize on our website. If you don't have an account yet, please register.
Post a resume