Quality Assurance Engineer - M/F/X

Neuchâtel

Key information

Publication date:24 January 2026
Workload:100%
Place of work:Neuchâtel

Job summary

Amaris Consulting is an independent consulting firm offering tech solutions. Join our global team of 7,600 talents and thrive!

Tasks

Ensure compliance and quality of operations and documentation.
Review deviations during production events for regulatory compliance.
Conduct investigations and define appropriate CAPA measures.

Skills

2-5 years of cGMP experience in pharmaceutical quality assurance.
Strong writing skills in French and English.
Ability to work collaboratively and autonomously.

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Who are we?

Amaris Consulting is an independent consulting and technology company serving businesses. With over 1000 clients worldwide, we have been deploying solutions for major projects for more than a decade - all made possible by an international team of 7,600 talents spread across 5 continents and more than 60 countries. Our solutions focus on four different business areas: Information systems and digital, telecommunications, life sciences, and engineering. We aim to create and develop a community of talents where all team members can reach their full potential. Amaris is your "stepping stone" to cross the rivers of change, to face challenges, and to successfully complete all your projects.

At Amaris, we are committed to offering our candidates the best possible recruitment experience. We seek to better know and understand our candidates, challenge them, and share our impressions as quickly as possible. Here is what our recruitment process looks like:

First contact: Our process usually starts with a brief virtual/phone conversation to learn more about you! The goal? To get to know you, understand your motivations, and ensure we offer you the position that best suits you!

Interviews (on average, the number of interviews is 3 – but it may vary depending on the seniority level required for the position). During the interviews, you will meet members of our team: your future manager of course, but also other people you will work with. These interviews will allow us to learn more about you, your experience and skills, but also about the position and what will be expected of you. Of course, you will also get to know Amaris: our culture, our history, our teams, and your career opportunities!

Case study: Depending on the position, you may be asked to take a test. This could be a role play, a technical evaluation, a problem-solving scenario, etc.

As you know, every person is different and the same goes for every role in a company. That is why we must adapt accordingly, so the process can sometimes be somewhat different for each person. That said, we always put ourselves in the candidate's shoes to offer the best possible experience. We look forward to meeting you!

Job description

We are currently looking for a Quality Assurance Engineer - M/F/X to ensure the compliance and quality of operations and information reported in various systems and documents, in accordance with the applicable standards.

🔥 Your responsibilities

Prepare, evaluate and approve controlled documentation (creation/revision)
Review deviations within production events in quality systems to verify their acceptability and compliance with procedures and regulatory requirements
Conduct or approve investigations, impact assessments (equipment/product/material) and define appropriate CAPAs
Participate in all meetings necessary to carry out the above tasks
Approve aseptic interventions performed during aseptic process simulations on site
Respect the escalation process
Ensure the completion of required training and management of software access according to internal policies
Occasionally contribute to other quality supervision activities (continuous improvement initiatives, GMP tours in classified areas, etc.)

🎯 Your profile

You have 2 to 5 years of operational cGMP experience in a Quality department on a pharmaceutical sterile product manufacturing site
You hold a master’s degree in engineering, science, technology or equivalent
You master all production processes (cell culture, aseptic filling, equipment, environmental controls, physicochemical and biological tests, etc.)
You have proven knowledge of Quality standards (cGMP) and quality systems (Deviations, CAPA, Change Control, Training, Documentation, etc.)
You have strong writing skills for documents in French and English
You are fluent in French and English
You demonstrate a strong ability to work in a team
You show agility and autonomy

💡 Our company culture:

Agility: Work in a flexible, dynamic, and stimulating environment.
International: Benefit from international collaborations and many mobility opportunities.
Intrapreneurship: Get involved in parallel initiatives or develop your own Business Unit.
Listening management: Receive personalized support throughout your professional journey.

Amaris Consulting is committed to diversity and inclusion. We encourage applications from all qualified individuals regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or any other characteristic.

Apply now and join our team for a rewarding and stimulating career!