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Post Market Surveillance Engineer II

Job in Plymouth, Hennepin County, Minnesota, USA
Listing for: Integer Holdings
Full Time position
Listed on 2026-07-13
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 85000 - 110000 USD Yearly USD 85000.00 110000.00 YEAR
Job Description & How to Apply Below

By living according to a common set of values, we create a culture that unifies, embraces the uniqueness we all bring to the company, and positions Integer for long‑term success.

At Integer, our values are embedded in everything we do.

Values
  • Customer
    :
    We focus on our customers' success
  • Innovation
    :
    We create better solutions
  • Collaboration
    :
    We create success together
  • Inclusion
    :
    We always interact with others respectfully
  • Candor
    :
    We are open and honest with one another
  • Integrity
    :
    We do the right things and do things right
What you’ll do in this role
  • The primary purpose of this job is to execute and support the Complaint Handling, Regulatory Reporting, and Post Market Surveillance processes for Integer under the direction, instruction and guidance from more experienced associates and managers in your organization. This position will be responsible for executing and providing support in the analysis, evaluation and product investigation of complaints received from external customers in a timely manner to comply with FDA 21 CFR (QSR) requirements and requirements of other regulatory bodies and countries with some instruction and guidance from more experienced associates and managers.
  • You adhere to Integer’s Values and all safety, environmental, security and quality requirements including, but not limited to:
    Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements.
  • Provide support of Integer’s Manufacturing Excellence and Market Focused Innovation Strategies.
  • Participation or Leadership in Site Hoshin Planning, Quality Planning, Validation master plans and associated quality improvement imperatives.
  • Support the standardisation of workplace organization & visual controls (5S), Manufacturing Standard Work, and robust training & certification programs where applicable.
  • Lead implementation of sustainability and continuous improvement initiatives.
  • Perform other duties as needed and as directed by your line of supervision.
Post Market Complaint Handling Activities
  • You will be responsible for accurately capturing and documenting all complaints in the complaint handling database according to internal policies and procedures.
  • You will be responsible for sending complaint acknowledgements to customers.
  • You will be responsible for tracking customer return products.
  • You will be responsible for performing complaint investigation activities with cross‑functional team members.
  • You will be responsible for reviewing device history records for nonconformities related to the alleged complaint.
  • You will interface with internal and external customers to gather additional information required for complaint investigations and prepare customer communication, complaint investigation reports and Customer Facing Reports, as applicable.
  • You will execute data collection, root cause investigations and resolution in support of a thorough complaint investigation related to product quality and patient safety.
  • You will play an active role in ensuring timely closure of complaint investigations to comply with requirements of FDA and other regulatory bodies and countries.
  • You may be required to handle, decontaminate, and analyze products used in the field by hospitals/end users per internal procedures and safety requirements, which will require you to have relevant vaccinations.
  • You will be responsible for performing risk assessments for products that are Integer owned designs.
  • You will be responsible for performing CAPA assessments and supporting CAPA investigations.
  • You will be responsible for assessing Adverse Event Reportability decisions in accordance with US and International regulations.
  • You will be responsible for assisting in the completion of applicable forms for submission of reportable complaints to applicable agencies.
  • You will assist in gathering complaint and ship data to support Post Market Trending, PMSRs, and PSURs.
  • You are expected to collaborate with others in the exchange of information, ask questions and regularly check for understanding in support of your development as a Post…
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