QC Specialist - Madrid, Spain at Project Delivery Partners

Madrid, Community of Madrid, Spain -

Full Time

Start Date

Immediate

Expiry Date

26 Sep, 26

Salary

0.0

Posted On

28 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Deviation Analysis, Environmental Monitoring, Water System Validation, Microbiology, Gas Analysis, CAPA Investigations, OOT/OOS Analysis, GMP Compliance, Root-Cause Assessment, Spanish Fluency, SOP Adherence, Data Interpretation

Industry

Pharmaceutical Manufacturing

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.

Responsibilities

The QC Specialist will perform and review deviation investigations, CAPAs, and Out-of-Trend analyses to ensure regulatory compliance. They will also execute environmental monitoring, water system validation, and microbiological testing within a regulated environment.