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Senior Validation Specialist

vor 1 Monat


Bern, Bern, Schweiz Agap2 Vollzeit

Overview of the Job

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We are seeking a skilled Senior Validation Specialist to join our team at Agap2. As a Senior Validation Specialist, you will be responsible for ensuring that our clients receive high-quality commissioning and qualification services.

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Job Description:

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The ideal candidate will have a strong background in life sciences or engineering and 2 years of experience in commissioning/qualification/validation activities in the pharmaceutical/biotech environment. You will be fluent in English and German and have a good knowledge of cGMP and regulatory requirements.

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Your main responsibilities will include designing and executing commissioning and qualification activities, including vendor supervision, installation, operational qualification, and support in execution of design qualification for other direct impact systems. You will also maintain control over activities and schedules with respect to relevant systems and actively participate in the development and delivery of deliverables.

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About Agap2

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Agap2 is a European engineering and operational consulting group founded in 2005. We specialize in various industries, including life science, energy, infrastructure, transportation, and chemicals. Our team is dynamic and committed to providing exceptional services to our clients.

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Why Choose This Job?

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This job offers a unique opportunity to work on challenging projects, collaborate with experienced professionals, and develop your skills. You will have access to training with accredited centers and enjoy a sustainable job with stability and real collaboration.

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What We Offer

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We offer a competitive salary of CHF 80,000 - 100,000 per year, depending on your experience. Additionally, you will have the opportunity to grow professionally and personally within our company.

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Requirements

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To be successful in this role, you must have a diploma in life sciences or engineering, a minimum of 2 years of experience in commissioning/qualification/validation activities, and excellent communication skills. You should also be fluent in English and German and have a good understanding of cGMP and regulatory requirements.

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How to Apply

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Only applications from Swiss and EU citizens will be considered. Please note that due to Brexit, we are no longer accepting applications from the UK. If you meet the requirements and are interested in this exciting opportunity, please submit your application.