QC Specialist

hace 2 días

Madrid, Madrid, España Project Delivery Partners A tiempo completo


Job Description:

PharmEng / Efor is a leading pharmaceutical and biopharmaceutical consulting company committed to providing innovative solutions to the challenges facing our industries. We pride ourselves on our dedication to quality, safety, and excellence in everything we do. As we continue to grow, we are looking for a highly qualified and motivated Automation Engineer to join our team.

Position: Quality Control Specialist

Experience Required: Minimum 5 years

Language Requirement: Fluent Spanish

Availability: Must be available to work on weekends, with uninterrupted commitment for at least 6 months.

Location: On-site

Overview

We are seeking a highly skilled QC Specialist
to support critical Quality Control operations within a regulated environment. The ideal candidate has extensive hands-on experience in deviation analysis, environmental monitoring, water system validation, microbiology, and gas analysis.

Key Responsibilities

  • Perform and review deviation investigations, CAPAs, and Out-of-Trend (OOT) analyses to ensure compliance and robust root-cause assessments.
  • Conduct on-site Quality Control activities, ensuring alignment with GMP and internal quality standards.
  • Execute and document Environmental Monitoring (EM) for classified and controlled areas.
  • Lead or support Water System Validation activities, including sampling, analysis, and performance qualification assessments.
  • Perform microbiological testing, method execution, data interpretation, and trend analysis.
  • Conduct gas analyses, ensuring accuracy and compliance with regulatory and internal specifications.
  • Collaborate with cross-functional teams to maintain quality oversight and support continuous improvement initiatives.
  • Ensure all QC operations are carried out according to SOPs, regulatory guidelines, and safety requirements.

Qualifications

  • Minimum 5 years of experience in Quality Control within pharmaceutical, biotechnology, or related regulated industries.
  • Fluent in Spanish (spoken and written).
  • Strong experience in deviation management, CAPA investigations, and OOT / OOS analysis.
  • Proven experience with Environmental Monitoring, microbiology, water system validation, and gas analysis.
  • Ability to work occasionally on weekends as required.
  • Strong analytical, organizational, and communication skills.

Join us: If you are a dedicated and highly motivated person with a passion for ensuring the highest standards of Quality Control in the Pharmaceutical Industry, we encourage you to apply. PharmEng / Efor offers a dynamic and inclusive work environment, competitive compensation, and opportunities for professional growth. Be part of our team and contribute to the success of our industry-leading solutions.

PharmEng/Efor is an equal opportunity employer and welcomes applicants from all backgrounds.

Thank you for your consideration and application We review all resumes and submissions, however, due to the high volume of applications we receive, only approved candidates will be contacted.


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