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Jobs at Noven Pharmaceuticals

Showing 9 JobsSort by:

Quality Specialist

  • Noven Pharmaceuticals

    • On-site
    • Jersey City, NJ

Director Clinical Pharmacology

  • Noven Pharmaceuticals

    • Hybrid
    • Jersey City, NJ

Technician II

  • Noven Pharmaceuticals

    • On-site
    • Miami, FL

Manufacturing Operator BC

  • Noven Pharmaceuticals

    • On-site
    • Miami, FL

QA Inspector

  • Noven Pharmaceuticals

    • On-site
    • Miami, FL

Service Desk Analyst

  • Noven Pharmaceuticals

    • On-site
    • Miami, FL

Associate Director Regulatory Affairs

  • Noven Pharmaceuticals

    • On-site
    • Jersey City, NJ

Laboratory Technician III

  • Noven Pharmaceuticals

    • On-site
    • Miami, FL

QA Inspector

  • Noven Pharmaceuticals

    • On-site
    • Miami, FL

1–9 of 9 jobs

Quality Specialist

  • Noven Pharmaceuticals

  • Jersey City, NJ 07097
Open in New Tab

On-site

Not Disclosed

Pharma

Quality

  • Posted on:
  • No. of Vacancies:

Job Description

Summary

Perform all activities related to investigation of customer complaints, process return samples for credit and reconcile call center complaints. Ensure on-time closure of complaint records and tasks associated with data requests from other departments. Identify critical complaints and prioritize these investigations to meet reporting requirements. Monitor complaint activity for trends and conduct trend investigations as appropriate. Generate and report metrics for monthly Council meetings, quarterly status meetings and annual product reviews. Participate and support in all team activities and projects as assigned.

Responsibilities
  • Initiate, investigate, summarize and close complaint records for Noven products using the TrackWise System.
  • Interact with individuals internally and externally to obtain information required for completion of complaint investigations.
  • Drive on-time closure of all complaint records and related tasks.
  • Identify critical complaints and complete investigations within required time period.
  • Generate and report complaint metrics in weekly progress reports and meetings.
  • Summarize complaint data for APR reports
  • Update and draft SOPs as deemed necessary.
  • Comply with all training requirements.
  • Comply with all Company policies and procedures, including safety rules and regulations including cGMPs, FDA regulations and other regulatory requirements.
  • Perform other duties and projects as assigned by the Director.
Qualifications

Education / Experience:

  • Candidate must have a Science degree, a background in the Pharmaceutical Industry and 3-5 years' experience in the processing customer complaints.
  • Must be computer literate and have good written and verbal communication skills; data entry experience and familiarity with TrackWise software or comparable system is a plus.
  • Must be detail-oriented to assure accuracy of completed tasks, and have the ability to work independently or in a team setting. Must be able to manage multiple tasks at a time and shift focus from one priority to another seamlessly.


Judgment / Decision Making:

Strong sense of ownership and accountability.


Work Environment:

Office environment.


Physical Demands:

Light lifting of file boxes.

Education

Degree

Bachelor

Specialization

Science
Experience:

3-5 yrs

  • Skills:
  • Complaint Investigation
  • TrackWise
  • CGMP
  • FDA regulations
  • Data Entry
  • SOP writing
  • Trend analysis
  • Written Communication
  • Verbal Communication
  • Attention to detail
  • Multitasking
  • Job Type:
  • Full-time
  • Shift Type:
  • Day shift

Compensation

  • Benefits:
  • 401K
  • 401K Match
  • Medical, Dental, Vision
  • Additional:
  • Base Salary

Job ID:

CGXP_26_29127

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