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QC Supervisor (Nights) at Medline Industries, Inc.

Posted in General Business 30+ days ago.

Type: Full-Time
Location: Waukegan, Illinois





Job Description:

Medline Industries, Inc. has an immediate opening for an QC Supervisor (6:00PM - 6:30AM, 4 Day working rotation) at our manufacturing facility in Waukegan, IL. The QC Supervisor will oversee and manage the Quality Control functions and personnel. The QC Supervisor's responsibilities include: inspection, product disposition, holding and releasing of product, defect investigation, segregation of defective product and/or raw materials, staffing and employee issues. Update policies and procedures as appropriate. In addition to exceptional leadership and analytical skills, you must have a "roll-up your sleeves" attitude.


  • Supervise and direct department employees so that work is accurate, timely and in accordance with company policies and procedures; monitor and evaluate subordinate performance and recommendations for merit increases.

  • Develop and mentor staff through on-boarding, open communication, training and development opportunities, performance processes; build and maintain employee morale and motivation; ensure the team is appropriately staffed with required competencies.

  • Prioritize work schedules. Schedule overtime as needed.

  • Maintain a good working relationship and open communications with Vice President of Operations.

  • Maintain open communications with each Branch Director and management team.

  • Train branch inspectors on Quality System Regulation (QSR)

  • Perform Line Audits to ensure acceptable product is being manufactured to specifications.

  • Conduct routine and non-routine analysis of in-process materials, raw materials, and finished goods.

  • Develop continuous improvements and/or cost/waste savings of existing process and products.

  • Investigate and resolve ongoing quality problems, such as defective raw materials and finished goods.

Medline offers a business casual, entrepreneurial work environment with strong growth potential, a competitive compensation package, and a complete benefits package including medical/dental/vision/life insurance; 401(k) with company match. And much more!Education


  • High school diploma or equivalent.
Relevant Work Experience

  • At least 3 years QC or similar experience.
  • Prior experience in medical device and/or drug manufacturing setting.
Additional

  • Intermediate level understanding of FDA/ QSR/ ISO14551 guidelines.
  • Intermediate level knowledge of ANSI/ ASQCZ1.4-current revision.
  • Intermediate Auditing Skills.
  • Intermediate level skill in Microsoft Excel (for example: using SUM function, setting borders, setting column width, inserting charts, using text wrap, sorting, setting headers and footers and/or print scaling).
  • Intermediate level skill in Microsoft Word (for example: inserting headers, page breaks, page numbers and tables and/or adjusting table columns).
Physical Requirements


  • Lift up to 60 pounds. Sit, walk or stand for prolong periods of time. Display specific vision abilities including, close vision, distance vision, depth perception and ability to adjust focus. Ability to work in hot and cold environments, (32F - 95F). Ability to encompass heights. Frequent bending and kneeling.
Preferred Qualifications

Education


  • Bachelor's degree.
Relevant Work Experience

  • Basic knowledge of Quality Systems Regulations and Medical Devices.
Certification / Licensure

  • Operating Material Handling Equipment.





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