Job Description
Job DescriptionConsultys is a global engineering and services consulting company dedicated exclusively to the Life Sciences industry.Since 2005, Consultys has been working on technical projects with some of the most sophisticated, innovative, and successful Life Sciences companies.
Do not wait to apply after reading this description a high application volume is expected for this opportunity.
Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada.Thanks to our excellent team, we support manufacturers in all stages of drug development.Respect, transparency, and gratitude.
These are the values that made Consultys one of the most high-performing Life Sciences consulting companies.Do you want to be part of a human-sized company that values every individual? Do you want to work on long-term innovative projects, working closely with global Life Sciences product companies in the world? Join us!We offer an attractive salary and benefits.
You will work in a stimulating environment, with a lot of opportunities for your professional and personal development.Job SummaryWe are seeking an experienced Commissioning, Qualification, and Validation (CQV) Engineer to join our team.
The CQV Engineer will play a crucial role in ensuring that all systems and equipment are properly commissioned, qualified, and validated according to industry standards and regulatory requirements.ResponsibilitiesLead CQV activities for pharmaceutical manufacturing projects.Develop and execute commissioning, qualification, and validation protocols.Ensure compliance with industry regulations and standards, such as cGMP and FDA guidelines.Collaborate with cross-functional teams to ensure the successful implementation of CQV activities.Conduct risk assessments and develop mitigation strategies.Document and report on CQV activities, findings, and corrective actions.Support continuous improvement initiatives related to CQV processes.QualificationsBachelor's or Master's degree in Engineering or a related field.Minimum of 5 years of industrial experience in CQV roles.At least 2 years of experience in the pharmaceutical industry.Strong understanding of industry regulations and standards.Excellent analytical and problem-solving skills.Effective communication and interpersonal skills.Ability to work effectively within cross-functional teams.
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