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Qa validation engineer

Lonay
Merz Aesthetics
EUR 95’000 pro Jahr
Inserat online seit: 13 Juli
Beschreibung

Join to apply for the QA Validation Engineer role at Merz Aesthetics

Join to apply for the QA Validation Engineer role at Merz Aesthetics

About Merz Aesthetics

Merz Aesthetics is a medical aesthetics business with a long history of empowering health care professionals, patients and employees to live every day with confidence. We aim to help people around the world look, feel and live like the best versions of themselves — however they define it. Clinically proven, its product portfolio includes injectables, devices and skin care treatments designed to meet each patient’s needs with high standards of safety and efficacy. Being family owned for more than 115 years, Merz Aesthetics is known for building unique connections with customers who feel like family. Merz Aesthetics’ global headquarters is in Raleigh, N.C., USA, with a commercial presence in 90 countries worldwide. It is also a part of Merz Group, which was founded in 1908 and is based in Frankfurt, Germany. Learn more at merzaesthetics.com.

About Merz Aesthetics

Merz Aesthetics is a medical aesthetics business with a long history of empowering health care professionals, patients and employees to live every day with confidence. We aim to help people around the world look, feel and live like the best versions of themselves — however they define it. Clinically proven, its product portfolio includes injectables, devices and skin care treatments designed to meet each patient’s needs with high standards of safety and efficacy. Being family owned for more than 115 years, Merz Aesthetics is known for building unique connections with customers who feel like family. Merz Aesthetics’ global headquarters is in Raleigh, N.C., USA, with a commercial presence in 90 countries worldwide. It is also a part of Merz Group, which was founded in 1908 and is based in Frankfurt, Germany. Learn more at merzaesthetics.com.

Position Snapshot


* Location: Lonay (Vaud, Switzerland)
* Activity rate: Full-Time
* Type of contract: Unlimited contract (CDI)


Key Responsibilities

As a QA Validation Engineer, you will be responsible for executing, drafting, and approving validation activities related to manufacturing, sterilization, cleaning, transport, and packaging processes, in compliance with FDA, GMP, and ISO 13485 requirements. You will also contribute to maintaining the validated state of processes, manage deviations and risk analyses, and support qualification activities for equipment, facilities, and computerized systems.

What Will Make You Successful

Knowledge & Skills

* Strong technical knowledge/expertise in production sites operating in a controlled environment
* Familiarity with equipment and BFU qualification
* Knowledge of sterilization and cleaning validation
* Strong interpersonal skills, ability to communicate with various internal and external stakeholders
* French / English proficiency
* Mastery of standard IT tools
* Strong writing skills and ability to summarize information effectively


Education & Qualifications

* University degree - Master's level or equivalent


Professional Experience

* Minimum of 3 years of confirmed experience in Quality or qualification/validation in the life sciences field (ideally medical devices)
* Knowledge of 21CFR Part 820 and ISO 13485 requirements


What We Offer

* Work-life balance: Our time is precious; to promote a good work-life integration, we allow flexible working hours and home office work, depending on the position requirements. Our employees also benefit from generous annual leave arrangements.
* Ongoing training: Your personal and professional development is key to our success. You will have access to multiple training programs (e.g., LinkedIn Learning, FranklinCovey, Harvard online) and development opportunities.
* Benefits: We offer various benefits, such as premium accident insurance, attractive Pension Fund, discounts programs, Employee Assistance Program, and regular fun team activities.
* Sustainable development: The Merz Group is investing at every site to achieve carbon neutrality by 2035.


Seniority level

* Seniority level

Mid-Senior level


Employment type

* Employment type

Full-time


Job function

* Job function

Engineering and Information Technology
* Industries

Pharmaceutical Manufacturing

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