QA Intern: Validation & Compliance Support

Thornton Tomasetti

Granada

On-site

EUR 10,000 - 15,000

Full time

14 days+
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Job summary

Abbott in Granada, Spain is offering a full-time internship focused on supporting the quality system at the Tech Center. The role involves assisting Validation activities, documenting protocols and reports, and supporting compliance and continuous improvement through internal audits.

The intern will collaborate with global cross-functional teams, gain exposure to GMP/GLP practices, and develop strong documentation and data-analysis skills in a dynamic health care environment.

Qualifications

  • Bachelor’s degree preferably BS or equivalent in Science, Engineering, Chemistry, Pharmacy, Biology or Microbiology.
  • Strong written and verbal communication skills.
  • Proficiency in Microsoft Office applications (Excel, Word, PowerPoint).
  • Ability to work effectively in a team environment and collaborate with cross-functional departments.
  • English: Advanced level (C1 or equivalent).

Responsibilities

  • Support to Validation area for: Validation documentation, protocols, final reports, Data collection and evaluation, Validation executions.
  • Support to compliance and continuous improvement: Participating in internal audits and periodic inspections to assure compliance with GMP/GLP.
  • Provide assistance to RD QA projects as assigned.

Skills

Attention to detail
Analytical skills
Organizational skills
Task management
Microsoft Office
Teamwork
Communication (written & spoken)
English (C1)

Education

Bachelor’s degree in Science, Engineering, Chemistry, Pharmacy, Biology or Microbiology

Tools

Microsoft Office

Job description

Abbott in Granada, Spain is offering a full-time internship focused on supporting the quality system at the Tech Center. The role involves assisting Validation activities, documenting protocols and reports, and supporting compliance and continuous improvement through internal audits.

The intern will collaborate with global cross-functional teams, gain exposure to GMP/GLP practices, and develop strong documentation and data-analysis skills in a dynamic health care environment.

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