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Quality Assurance/Complaints - Senior Associate

ApTask

Thousand Oaks (CA)

On-site

USD 65,000 - 85,000

Full time

23 days ago

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Job summary

A leading company in IT Services and Consulting is seeking a Senior Quality Assurance Associate to join their team. The ideal candidate will have a Bachelor's degree in life sciences and 2+ years of experience in quality assurance within the GMP pharmaceutical or medical device industry. Responsibilities include evaluating product complaints and authoring technical reports. This entry-level contract position offers a dynamic work environment focused on quality and compliance.

Qualifications

  • Typically 2+ years of related quality assurance or manufacturing experience.
  • Basic statistical skills including data trending.

Responsibilities

  • Receive, clean, and evaluate product complaint return samples.
  • Author technical assessment reports.
  • Interface with various sites and business partners.

Skills

Self-motivated
Attention to details
Strong communication
Collaboration

Education

Bachelor’s degree in life sciences

Job description

Quality Assurance/Complaints - Senior Associate

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Recruitment Executive at Omiz Staffing Solutions/ApTask

Bachelor's degree. Nice to have: documentation practices, GMP, previous lab experience.

Hiring Manager Intake Notes

  • What qualities/characteristics are you looking for in candidates? Self-motivated individuals interested in gaining expertise in a fast-paced environment
  • When reviewing resumes, what stands out? GDP experience, complaints experience are a plus
  • What is the minimum education and experience? Bachelor’s degree in life sciences
Responsibilities:
  1. Receive, clean, and evaluate product complaint return samples
  2. Interface with various sites and business partners
  3. Author technical assessment reports
Requirements:

Bachelor's Degree in Life Sciences or related field or the equivalent combination of education and/or experience. Typically 2+ years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Evaluate documentation and operations according to company guidelines. Be self-motivated, attentive to details, and able to prioritize and meet deadlines. Basic statistical skills including data trending. Basic project management skills. Ability to understand, follow, and implement instructions independently. Strong communication, collaboration, word processing, database, and spreadsheet skills. Good organizational skills to manage multiple projects. Role may involve prolonged sitting, standing, lifting up to 50 lbs, and transporting samples across campus.

Additional Details:
  • Seniority level: Entry level
  • Employment type: Contract
  • Job function: Quality Assurance
  • Industries: IT Services and IT Consulting

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