Complaint/Adverse Event Coordinator

New York  ‐ Onsite
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Keywords

Description

DESCRIPTION

The Complaint/Adverse Event Coordinator will investigate international and domestic complaints/adverse events in accordance with cGMP requirements.

Responsibilities
  • Generate appropriate reports.
  • Perform QA investigations for clinical and non-clinical complaints/adverse events by reviewing batch records, examining retention samples, inspecting returned product, and obtaining laboratory analysis or forensic testing, as necessary.
  • Prepare complaint reports and submit to Product Quality by assigned due dates.
  • Review packaging, manufacturing, and shipping processes/records and request investigation reports when necessary.
  • Interact with manufacturing/packaging areas (Pearl River, Montreal, or other applicable sites) on product investigations.
  • Maintain investigation records by creating and maintaining a paper file system and entering data into the WATSIN/PCOM 3.0 database systems, as required. This includes lot identification, manufacturing/batch record review, retention examination, returned sample evaluation, correspondences, phone conversations, and investigation reports.
  • Review and revise complaint/adverse event/departmental Standard Operating Procedures.
  • Prepare complaint investigation section for annual product reviews.
  • Assist in preparation of monthly reports when necessary and perform trend analysis and data searches, when necessary.
  • Work closely with manufacturing/packaging operations, and forensic testing laboratories, as applicable, to provide Quality oversight and support to complaint investigations.
  • Participate in meetings and project teams and assist in issue resolution.

Qualifications

  • Pharmaceutical experience a must
  • BS preferably in Pharmacy (BS in Chemistry or Biology acceptable) with 3 years of experience in complaint/adverse event investigations or MS with 2 years of Quality experience as listed above.
  • Investigation background, complaints processing, and excellent writing skills preferred.
  • Experience with WATSIN complaint database, in particular the use of trending and tracking tools.
  • Experience in managing/coordinating the complaint process from receipt of complaint to completion.
  • MS Word expertise.

SKILLS
Pharmaceutical experience, BS preferably in Pharmacy, Experience with WATSIN complaint database, MS Word

Synectics offers competitive salaries and a full suite of benefits. EOE.

Start date
n.a
From
Generic Network
Published at
29.10.2011
Project ID:
261012
Contract type
Freelance
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