Senior CQV 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

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Qualification & Validation, Sterile Injectable Manufacturing, HVAC Qualification, Environmental Monitoring, GMP Compliance, Annex 1 Guidelines, Risk Assessment, CAPA Management, Change Control, Aseptic Processing, Cleaning Validation, Sterilization Validation, URS/DQ/IQ/OQ/PQ, Technical Leadership, Cross-functional Collaboration, Audit Support

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 Senior CQV Consultant to join our team. Position Title: CQV Expert Location: Madrid Type of Contract: Full-Time / On site Position Summary: The Senior Consultant in Qualifications & Validations is responsible for leading and executing validation activities across sterile injectable pharmaceutical operations. This includes equipment, utilities, facilities, and process qualifications, with a strong focus on environmental monitoring and HVAC systems. The role supports multiple sites and projects, ensuring compliance with GMP and global regulatory standards, while providing strategic guidance and technical leadership. Key Responsibilities: Lead qualification protocols (URS, DQ, IQ, OQ, PQ) for sterile manufacturing equipment, cleanrooms, HVAC systems, autoclaves, and utilities. Develop and review validation master plans, risk assessments, and lifecycle documentation for injectable processes. Oversee process validation, cleaning validation, and sterilization validation in aseptic environments. Design and implement environmental monitoring programs, including viable and non-viable particle control, alert/action levels, and trending. Qualify HVAC systems including airflow visualization, pressure differentials, filter integrity testing, and temperature/humidity mapping. Ensure compliance with global regulatory requirements (FDA, EMA, WHO, PIC/S) and Annex 1 guidelines. Collaborate with cross-functional teams (Engineering, QA, QC, Manufacturing, Regulatory Affairs) to align validation strategies. Support audits and inspections by providing validation documentation and expert responses. Manage and resolve deviations, CAPAs, and Change Controls related to qualification and validation activities. Provide technical training and mentoring to client teams on validation and environmental control best practices. Prepare detailed reports and executive summaries for internal and external stakeholders. Travel to client sites for project execution, troubleshooting, and validation support. Qualifications: Bachelors or masters degree in Pharmacy, Biotechnology, Engineering, or related scientific discipline. Minimum 8 years of experience in pharmaceutical validation, with a strong focus on sterile injectable products. Deep understanding of aseptic processing, cleanroom classification, HVAC qualification, and contamination control. Proven experience in environmental monitoring program design and execution. Strong knowledge of GMP, Annex 1, ICH Q8-Q10, and validation lifecycle principles. Hands-on experience with CAPA management and Change Control systems. Demonstrated ability to lead cross-functional teams and mentor junior staff. Excellent communication and documentation skills. Fluent in Spanish and English (advanced or native level required). Willingness to travel. Preferred Experience: Experience with injectables. Strong understanding of aseptic processing, terminal sterilization, and cleanroom operations. Proven track record managing injectable products, and QA-related activities. Hands-on experience with CAPA systems, Change Control management, and quality documentation workflows. What We Offer: Competitive compensation based on experience and project scope Exposure to international pharmaceutical operations and regulatory environments Opportunity to lead high-impact injectable validation programs Flexible work arrangements and travel support Collaborative and technically driven work culture Join us: If you are a dedicated and highly motivated individual with a passion for ensuring the highest standards of Engineering and Quality 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

Lead and execute validation activities for sterile injectable pharmaceutical operations, including equipment, utilities, and HVAC systems. Ensure global regulatory compliance while providing strategic technical leadership and mentoring to client teams.