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Quality Complaints, Senior Associate, GMP​/Medical Device; JP

Job in Thousand Oaks, Ventura County, California, 91362, USA
Listing for: 3key Consulting, Inc.
Full Time position
Listed on 2025-12-01
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
    Data Scientist, Medical Science
Job Description & How to Apply Below
Position: Quality Complaints, Senior Associate, GMP/Medical Device (JP10246)
Job Title:Quality Complaints, Senior Associate, GMP/Medical Device(JP10246)
Location:Thousand Oaks, CA.
Employment Type:Contract
Business Unit:Product Complaints & Surveillance
Duration:1+ years with likely extensions or conversion to FTE
Notes:100% onsite
Posting Date:05/11/2022

3 Key Consulting is hiring
Quality Complaint Senior Associate
for a consulting engagement with our direct client, a leading global biopharmaceutical company.

Job Description:
Requirements:
  • Bachelor's Degree in Life Sciences or related field or the equivalent combination of education and/or experience.
  • Typically 2 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry.
  • Evaluate documentation and operation according to company guidelines.
  • Be self-motivated, attentive to details and able to prioritize and meet deadlines. Basic statistical mathematical skills including the ability to trend data.
  • Basic project management skills. Independently understand, follow and implement instructions. Written and verbal communication & collaboration skills.
  • Strong word processing, database and spreadsheet application
Skills:
Strong organizational skills with the ability to manage multiple projects or assignments. Role may involve periods of prolonged sitting and standing. Role may involve lifting boxes and storage containers of up to 50lbs. Role may involve transporting samples to different buildings across campus.

Top Must-Have Skill Sets:
  • Attention to detail in lab environment
  • Proficient in MS office
  • Strong written and verbal communication skills
  • Understanding GMP
  • Background in quality inspection high plus
Day to Day Responsibilities:
  • Receive, clean, evaluate, and file/store returned samples
  • Operate equipment such as cameras, biosafety cabinets, xrays
  • Manage inventory of consumables
  • Interface with complaint owners and cross functional team members
  • Prepare samples for shipment to other locations
Employee Value Proposition:
Career growth/ opportunity

Red Flags:
Candidate needs to have strong attention to details

Interview process:
2 Web Ex interviews & 1 Onsite interview

We invite qualified candidates to sendyour resume to. Ifyou decide that you’re not interested in pursuing this position, please feel free to take a look at the other positions on our  You are welcome to also sharethis opportunity with anyone you think might be interested in applying for this role.
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Position Requirements
10+ Years work experience
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