QA Document Control Coordinator

Purpose

Supervise and coordinate all activities related to the document control system at Microtek Medical Holdings, Inc (Jacksonville) facility.

Equipment

• Tape Measures
• Force Gauge (Chatillon)
• Calipers

Position Responsibilities

• Responsible for typing, maintaining and distributing procedures.
• Responsible for making necessary changes to Quality System documents (WI, SOPs & Forms).
• Maintain and organize the document control area.
• Act as a liaison with Columbus’ Technical Service and Specification Department and Jacksonville Facility.
• Maintain accurate CAPA, Complaints, Internal Audits, Management Review Meeting, MRB and Finished Goods Scrap Authorization files.
• Perform verification tasks relating to product specifications.
• Perform disposition of Return Goods (RMA).
• Generate monthly RMA report.
• Conduct in-process inspections among all process performed within the Pack Out department.
• Maintain the equipment calibration list and assure all equipment used are within calibration date.
• Perform other duties in which employee has training and/or skills necessary to perform tasks successfully.

Qualifications / Competencies

• Associate’s degree (A.A.) or equivalent from a two year college or technical school or six months to one year related experience and/or training or equivalent combination of education and experience.
• Familiarity with FDA/ISO regulations.
• Basic computer knowledge including Word and Excel.
• Good communication and mathematical skills.
• Knowledge of the use of some measurement equipments.

Physical Demands

• Stand, sit, stoop, kneel, and crouch.
• Frequent lifting.
• Reference Physical Requirements Checklist.

Work Environment

• Regularly exposed to moving equipment.
• Regularly exposed to extreme cold and heat.
• Noise level is usually moderate.

Location

Jacksonville, FL

How to apply

If you are interested in applying for this position please visit our ONLINE JOB APPLICATION FORM.

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