Pauwels Consulting

HVAC Validation Analyst

Posted: just now

Job Description

Join a professional environment that aims for the highest degree of operational excellence in healthcare production. Here, your expertise will be essential in transforming raw materials into life-saving medications through a series of complex production steps.We are looking for a dedicated HVAC Validation Analyst Consultant to join our Utilities team. The ideal candidate will be involved in validating equipment, environments, and HVAC systems to ensure compliance and reliability.You independently plan, monitor, and execute routine validation programs for equipment, HAC filters, laboratory and production devices, and temperature-controlled areas.You prepare validation worksheets and manage approval and classification processes according to correct procedures.You input data and manage all completed validations in the specified software.You initiate and monitor quality deviations, reporting discrepancies in conducted validation studies.You collaborate and establish agreements with various departments (production, QA, laboratory…) during the execution of studies and while reviewing and approving results.You are responsible for ensuring complete availability of validation devices.You follow up and appropriately process validations conducted by external companies.You assist colleagues in conducting and processing validation studies.What are we looking for?You hold a Bachelor's degree in a scientific field or have equivalent experience.You have a strong understanding of English (written and spoken).You possess strong interpersonal skills and are a team player.You are an effective communicator.You are organized, accurate, and quality-conscious.You have analytical skills and problem-solving abilities.You have experience or knowledge of temperature mapping and/or validation.You have experience or knowledge in performing filter integrity tests.You have experience or knowledge of HVAC systems operation.You have experience in a similar role within a quality or production environment.You have experience within a GMP environment.You are familiar with cGMP and RFT.You are open to junior to senior levels, with corresponding experience levels ranging up to 575€.

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