Quality Control Supervisor

Medline; Tinton Falls (NJ); On-site; USD 60,000 - 85,000; Full time

Job summary

Medline in Tinton Falls, NJ seeks a Quality Control supervisor to oversee QC functions at the distribution center. You will manage performance, attendance, and reviews; schedule overtime; and train staff on QSR/ISO requirements.

The role requires strong FDA/QSR/ISO-13485 knowledge, experience in medical device/drug manufacturing, and ability to lift up to 50 pounds. Travel may be needed.

Qualifications

• Education: High school diploma or equivalent.
• At least 3 years QC or similar experience.
• Prior experience in medical device and/or drug manufacturing setting.
• Intermediate knowledge of FDA/QSR/ISO-13485 guidelines.
• Intermediate knowledge of ANSI/ASQC Z1.4-current revision.
• Ability to lift up to 50 pounds; sit/stand; capable of travel.

Responsibilities

• Manage performance, attendance, monthly bonus and reviews for direct reports.
• Prioritize work schedules and schedule overtime as needed.
• Maintain open communications with Branch Management.
• Train inspectors on QSR and Board of Pharmacy rules.
• Support Quality, Regulatory and Operations to ensure regulatory compliance.
• Lead day-to-day activities and provide input into hiring decisions.
• Operate material handling equipment as necessary.

Skills

Quality Control

Team leadership

Regulatory knowledge

Microsoft Excel

Microsoft Word

Physical stamina

Education

High school diploma or equivalent

Associates degree or technical certification preferred

Tools

Microsoft Excel

Microsoft Word

Job description

Oversee and manage the Quality Control functions and personnel at designated distribution center. Responsibilities Include inspection, product disposition, holding and releasing of product and personnel matters.

Hours: 5:30pm-5:30am

Job Description

MAJOR RESPONSIBILITIES

• Manage all performance, attendance, monthly bonus and employee reviews for direct reports at designated distribution center.
• Prioritize work schedules. Schedule overtime as needed.
• Maintain a good working relationship and open communications with Branch Management.
• Train branch inspectors on Quality System Regulation (QSR), Department of Health/ Board of Pharmacy rules and regulations.
• Support Quality, Regulatory and Operations to ensure branch compliance with all applicable regulations.
• Lead day-to-day activities of employees. Assign, monitor and review progress and accuracy of work, directs efforts and provides technical guidance on more complex issues. Provide input into hiring, firing and performance reviews.
• Operate material handling equipment as necessary to support workload and overall projects.

MINIMUM QUALIFICATIONS

• Education High school diploma or equivalent.

Work Experience

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

Knowledge / Skills / Abilities

• Intermediate level understanding of FDA/ QSR/ ISO-13485 guidelines.
• Intermediate level knowledge of ANSI/ ASQCZ1.4-current revision.
• 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).
• Ability to lift up to 50 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, (32F95F). Ability to encompass heights. Frequent bending and kneeling. Must be available to travel from state to state on occasion.

PREFERRED QUALIFICATIONS

• Education Associates degree or technical certification preferred.