Indrotec - Staffing and Workforce Management

Production Supervisor

7 days left

Location
Maple Grove, MN, United States
Salary
Contact For Rate
Posted
Jun 22, 2017
Closes
Jul 01, 2017
Ref
814651-03
Job Type
Temporary
Employment Status
Full Time
Job Description:

Indrotec Staffing and Workforce Management is seeking qualified candidates to work as a Production Supervisor for a Medical Device Company. This position is located in Maple Grove.

This position is responsible for supervising associates on assigned shifts to ensure quality, production results and safety. Monitors work flow, schedules and works cooperatively across all shifts and departments.

This is a great contract to hire opportunity.
Qualified candidates will have the following skills and abilities:
Formulate partnerships across shifts/departments to initiate and foster a spirit of cooperation and deliver value added work that reflects the business objectives of the organization

Accomplish production results by communicating job expectations; planning, monitoring and appraising job results; coaching, counseling and disciplining associates; recommending, assisting in developing and consistently enforcing policies and procedures

Provide production information to business partners when requested by compiling, sorting, analyzing and presenting production performance records and data

Maintain work flow by monitoring the steps of the process; evaluating job cycle times; observing control points and equipment and facilitating corrections to malfunctions as required; monitoring associates and resources; studying methods; recommending cost reductions; developing reporting procedures and systems

Work in cooperation with EHS and Engineering to identify significant environmental impacts of plant operations and to establish goals and targets to improve safety, minimize impact on OSHA logs and reduce lost work day cases

Coordinate with other shift supervisors to achieve consistency and best practice production results

Conduct performance management discussions and effective, thorough and objective investigations; properly document and resolve issue

Develop Leads by providing them with new opportunities to grow in their positions and by challenging them while holding them accountable for results.

Conduct performance reviews on all assigned associates

? Other responsibilities may be assigned & not all responsibilities listed may be assigned


Requirements:
• Bachelor degree or equivalent experience

• 1 year of current or past lead experience

• Prior experience in the medical device industry is preferred

• Proficient in Microsoft Office

• Good team relationship and interpersonal skills

• Experience working in quality-driven process environment, ISO knowledge preferred

• Excellent written and oral communication skills
Schedule:
2nd Shift

2:15pm - 10:15pm, must be available for overtime as required

Compensation is dependent on experience $50,000-65,000/year

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