RealDuration: 12 Months (possible extension)
Are you an experienced Validation Engineer passionate about quality, compliance, and improving pharmaceutical manufacturing processes? We are looking for a driven professional to support and lead equipment qualifications and validation activities in a dynamic GMP environment.
Lead and execute IQ, OQ, and PQ qualification activities.
Support validation and requalification efforts for steam sterilizers/autoclaves, lyophilizers, depyrogenation tunnels, and airflow visualization/smoke studies.
Document, track, and close deviations and change controls.
Provide technical guidance to project teams and stakeholders on validation-related topics.
Ensure alignment of validation activities with production schedules and project timelines.
Perform risk assessments and impact analyses, proposing effective mitigation strategies.
Draft, review, and evaluate validation data, reports, deviations, and periodic reviews in line with GMP/GDP standards.
Act as a Subject Matter Expert (SME) during internal and external audits/inspections.
Mentor and train junior validation team members.
Bachelor's degree or higher in a relevant engineering or scientific field.
4-5 years of experience in validation or CQV within the pharmaceutical industry.
Strong understanding of GMP, V-Model, and SDLC methodologies.
Excellent analytical, problem-solving, and organizational skills.
Team-oriented mindset with a proactive "can-do" attitude.
Strong communication skills and the ability to work effectively with cross-functional teams.
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