Sr. Supervisor Production

Intuitive•Peachtree Corners, GA

1d•$99,700 - $168,700•Onsite

About The Position

The primary objective for this role is to lead and supervise the technicians on assembly line(s) which build a variety of products. The primary focus is on achieving safety and quality goals while simultaneously meeting team performance goals for production. These goals will include: efficiency, FPY, hours accuracy, scrap, time lost accuracy, DHR accuracy/PL accuracy, and first pass cycle yield. The senior supervisor works closely with Assembly Technicians, Engineers, Group Leads, Trainers, and manufacturing management to achieve team performance goals.

Requirements

Experience in the medical device industry is preferred.
Strong working knowledge of Lean Manufacturing, and 6-sigma. Demonstrated experience in leading various Lean Manufacturing initiatives or projects.
Experience in leading new product transfers into Manufacturing.
Expert in SAP and Agile.
Expert in the use of personal computers to perform daily work. Familiar with the Microsoft Office suite of programs and MRP systems.
Superb communication skills, including written and verbal instruction.
Ability to work in a fast-paced and multi-focused work environment.
Ability to lift 50lbs.
Able to use office and test equipment in a typical office/light manufacturing environment.
Repetitive motion. Keyboard and computer motion.
Vision abilities required include close, distance, color, depth and ability to adjust focus.
Typical production & repairs environment.
High urgency and occasional stress associated with customer deadlines.
Some risk of exposure commonly used chemical compounds such as epoxy, denatured alcohol and acetone.
Willing and able to work extended hours when necessary.

Nice To Haves

The ideal candidate will have a love for a fast-paced and multi-focused work environment.
Extensive knowledge of the PDCA cycle and other advanced lean tools.
Ability to implement visual displays, 5s, TPM, Kanban, CI, and COMMWIP with minimal guidance.
Proven experience with people management, conflict resolution and risk management.
Experience with non-conformance investigations and ECO's.
Experience in the medical device industry is preferred, specifically in the area of high volume instrument manufacturing.

Responsibilities

Conduct root cause analysis autonomously.
Participate in lean initiatives and implement changes with guidance.
Review/approve ECOs, assess manufacturing impact, and use Microsoft Office and MRP systems for data reporting.
Understand quality systems and ensure compliance during internal/external audits.
Participate in cross-functional projects, coordinating tasks with some oversight.
Plan individual tasks, use project management tools, and create task implementation plans with direction.
Review and present manufacturing and quality metrics, escalating when necessary.
Set and communicate goals with some mentorship, aligning team goals with corporate priorities, and recognize outstanding performance.
Identify and escalate conflicts with mentorship, learning to spot early indicators.
Identify team stars, create development plans with mentorship, and set effective personal goals.
Make efficient recommendations with minimal oversight, understanding the reasons and priorities behind projects.
Mitigate risks by reviewing lessons learned and similar projects.
Advise peers and drive project teams, execute improvements, and present effectively to management.