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Open nowFirst seen 16 hours ago

Post Market Surveillance Coordinator II

Phantom Staffing73 open roles

Where
Chelmsford, Massachusetts, United States
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Your applicationOpen nowPost Market Surveillance Coordinator IIPhantom Staffing · Chelmsford, Massachusetts, United States

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on Phantom Staffing's own form.

The reply lands in your private mailbox

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The clock on this job

Early applications get read.

11.3% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 2.0%1 day
  2. 4.2%3 days
  3. 11.3%7 days
  4. 17.6%14 days
  5. 34.3%30 days
  6. 43.5%60 days
This job: first seen 16 hours ago

The posting

Essential Functions:

  • Maintain Post Market Surveillance documentation in accordance with procedures and Regulatory requirements to stand on its own in the event of an audit.
  • Complete and submit documentation for reportable events to Competent Authorities within required timelines, including but not limited to FDA-3500A MedWatch Reports, Manufacturing Incident Reports for EMEA Vigilance (both MDD and EU MDR), MDPR for Health Canada, etc.
  • Coordinate and maintain closure of complaint records in our Post Market Surveillance system.
  • Maintain the storage and retrieval of active and inactive complaint records.
  • Provide support for Post Market Surveillance activities.
  • Support the review and evaluation of customer communications for complaint reporting obligations.
  • Communicate and correspond with customers.

Required/Preferred Education and Experience:

  • High School required
  • 1-3+ years Healthcare or Medical Device Industry preferred
  • Regulatory certification exposure to Post Market Surveillance Preferred
  • Knowledge, Skills and Abilities
  • Has Knowledge of FDA QSR, 803, MDD, MDR, ISO13458 and MDSAP is preferred. 2-5 years experience in an FDA and ISO regulated environment preferred.
  • Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
  • Ability to work in collaborative and independent work situations and environments with minimal supervision.
  • Attention to detail/Quality work.
  • Ability to manage Time effectively.
  • Positive attitude/Forward thinker.
  • Analytical/ability to take initiative to correct problems.
  • Quality or Regulatory experience in Medical Device Experience preferred.
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