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Manufacturing Supervisor - 2nd shift PDF

Medtronic
North Haven, CT 06473
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Manufacturing Supervisor - 2nd shift PDF

Location:

North Haven, Connecticut, United States

Requisition #:

20000AOS

Post Date:

Jul 15, 2020


**Careers that Change Lives**


Your dedication to quality is important to our customers and, most importantly, to their patients. As the Manufacturing Supervisor, you will directly supervise and lead 53 hourly employees while achieving quality and production objectives for the PDF Group in General Surgical Products.


Do meaningful work, make a difference, and improve lives starting with your own.


The Minimally Invasive Therapies Group strives to enable earlier diagnosis, better treatment, faster complication-free recovery, and enhanced patient outcomes through less invasive surgical solutions.


SURGICAL INNOVATIONS sets the standard for Minimally Invasive Surgery (MIS) by creating innovative surgical products and services that focus on obesity and diseases and conditions of the gastrointestinal tract, lung, abdominal wall, pelvic region, and the head and neck.


We value what makes you unique. Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.


**A Day in the Life**


Reporting to the Production Manager, the 2nd Manufacturing Supervisor will ensure compliance with Quality System Regulations (QSRs) and International Organization for Standardization (ISO) while promoting World-Class Manufacturing. You will lead and develop an environment which fosters teamwork and innovation performance management inclusive of administration of company policies and procedures, and safety and good housekeeping.


You will oversee your assigned Focus Factory which includes Assemblers, Manufacturing Employees, and Team Leaders. You will lead your team to successfully manage performance, develop talent, support and encourage engagement and inclusion, communicate business and operational developments while planning and prioritizing the teams output.


**You will:**


Drive a culture where Safety and Quality are the norm throughout the Manufacturing Department including compliance to all laws, regulations and standards. Ensure manufacturing practices are consistent with Medtronic Policies and Procedures and relevant Food and Drug Administration (FDA), ISO, and OSHA guidelines and regulations.


Manage, monitor, mentor, and support the activities of direct reports to ensure focus factory and personal development objectives are met.


Drive continuous improvement throughout the Manufacturing Department using training, Operational Excellence tools and other methods


Provide effective training, clear performance expectations, specific feedback on behaviors, effective coaching and mentoring, identifying and providing developmental opportunities, and accurate, timely performance appraisals.


Develop and prioritizes schedules and manpower requirement for assigned areas.


Strive to improve the skills of associates by providing clear performance expectations, specific feedback on behaviors, effective coaching and mentoring, identifying and providing developmental opportunities, and accurate, timely performance appraisals.


Provide appropriate responses and support when involved in NCRs or CAPAs; verifies solutions.


Control further processing, delivery or installation of non-conforming product until it is corrected.


**Must Have:**


Minimum Qualifications


Bachelor's Degree plus 1 year relevant supervisory experience.


**Nice to Have:**


3-5 years solid supervisory experience in a Manufacturing setting


Experience in a regulated manufacturing work environment.


Previous experience implementing Lean Manufacturing Projects.


Effective written and verbal communication skills, interpersonal skills, and demonstrated ability to interact and interface with production personnel as well as management.


Strong computer software capability and experience with manufacturing management systems


Knowledge and experience in Material Requirements Planning (MRP), Barcode labor tracking/material tracing, Statistical Process Control (SPC)/Defect tracking, FDA, ISO, and Device History Record (DHR) requirements and regulations, Just-In-Time (JIT) inventory practices, Good Manufacturing Practices, OSHA and basic Cost Accounting.
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

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Posted: 2020-07-17 Expires: 2020-09-25
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Manufacturing Supervisor - 2nd shift PDF

Medtronic
North Haven, CT 06473

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