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Quality Assurance Manager

Quality Assurance Manager

EndogenexPlymouth, MN, United States
6 days ago
Job type
  • Full-time
Job description

PRIMARY FUNCTION

Responsible for implementing and performing quality system processes that ensure Endogenex meets requirements of internal procedures and applicable external standards / regulations (including but not limited to ISO 13485, 21 CFR 820,806 and 803, EU MDR, MDSAP).

PREFERRED QUALIFICATIONS

  • Bachelor's degree with 7+ years of quality experience in medical device and / or comparable regulated environment
  • Familiarity with applicable external standards / regulations (ISO 13485, USA, EU MDR, MDSAP, UK and Australian)
  • Strong interpersonal, organizational, and technical writing skills
  • Strong communication and leadership skills, with the ability to work effectively in a fast-paced, collaborative environment.
  • Ability to manage multiple priorities with commitment and performance to deadlines
  • Experience with implementing and completing activities that maintain compliance with document control requirementsand quality system management software systems (experience with Grand Avenue preferred)
  • Experience implementing and completing activities related to Post Market Surveillance, Complaints, CAPAs, andNonconformances along with corresponding risk management determinations
  • Strong computer skills and statistical trending techniques

RESPONSIBILITIES :

  • Implement and maintain document control and assigned portions of the quality system in compliance with applicable regulations and standards.
  • Processing document change requests, including reviewing for completeness, managing approvals, releasing documents, and managing document control assigned tasks following document release.
  • Responsible for all manufacturing and quality system trending and post-market surveillance activities.
  • Responsible for generating and managing all NCM and Servicing files .
  • Performs all quality system metric recording and report records.
  • Tracking and trending CAPAs, nonconformances, complaints and other quality system monitoring.
  • Implements complaint investigation process, including but not limited to complaint file documentation, departmental coordination, proper escalation, and initial reporting assessments.
  • Appropriately identifies outputs from work processes which drive additional efforts within the product lifecycle including but not limited to risk management updates, management review recommendations and quality system alert / alarm levels.
  • Manage calibrated equipment, including tracking when calibration is due, coordinating completion of calibration, and reviewing calibration certificates for accuracy without impacting production or R&D programs.
  • Manage employee training files and training program, ensuring employees stay up to date with required training. Lead efforts in streamlining and incorporating training material updates as required.
  • Manage creation, implementation, and ongoing monitoring of supplier and part approvals
  • Manage return material authorization (RMA) process.
  • Assist in preparation of management review presentations.
  • Tracking release of and coordination with affected department for implementation of new standards. Provide gap analysis assessment reports to affected departments.
  • Performs product dispositioning documentation on behalf of quality and execute quality assurance in return / service / rework programs - This includes responsibility for certificates of conformance approvals and finished goods inspection and lot release.
  • Performs all device related inspection procedures requiring quality oversight and approval
  • Supports production quality documentation retention for finished goods
  • Perform other duties and responsibilities as assigned.
  • Special Physical Demands and Working Conditions

    1)  Physical demands : While performing the duties of this job, the employee is occasionally required to walk; sit; use hands to finger, handle or feel objects, tools, or controls; reach with hands and arms; balance; stoop; talk and hear. Specific vision abilities required by the job include close vision and distance vision. Ability to occasionally lift and / or move up to 35 pounds.

    2)  Work environment : Fast paced work environment. While performing the duties of this job, the employee will experience in / out of the office noise at a minimal level. Must be capable of transporting self to various business locations. If using your own motor vehicle, must have a current, valid state driver’s license and proof of insurance coverage that at least meets current residence’s state minimum requirements. US and OUS travel may be required.

    Job Type : Full-time

    Benefits :
  • 401(k)
  • Dental insurance
  • Health insurance
  • Paid time off
  • Application Question(s) :

  • Do you live within driving distance of Plymouth, MN, zipcode 55441?
  • Education :

  • Bachelor's (Required)
  • Experience :

  • Quality systems : 5 years (Required)
  • Work Location : In person
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    Quality Assurance Manager • Plymouth, MN, United States

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