Deviations Management Expert
Solliciteren
Plaats
Brussel1000
Brussel
België
Contract
Vooltijds, Onbepaalde duurDatum gepubliceerd
2026-02-18Online to:
2026-04-19EUR 20.00 HOUR
Deviations Management Expert
Deviations Management Expert
Brussels Area, Belgium
About Nalys
Nalys is a fast-growing consultancy company dedicated to delivering high‑value expertise across the life sciences and high‑tech engineering sectors. Our mission is to empower our consultants and partners by combining deep technical knowledge with a human‑centric approach. Joining Nalys means becoming part of a dynamic, supportive, and innovation‑driven community where your impact truly matters.
We are currently looking for a Deviations Management Expert to support one of our pharmaceutical partners located near Brussels. This role is an excellent opportunity for a quality professional eager to drive continuous improvement and strengthen deviation governance within a highly regulated environment.
Your Responsibilities
As a Deviations Management Expert, you will play a key role in ensuring robust deviation governance and enhancing process performance. Your main responsibilities include:
Deviation Process Governance & Performance
Oversee and continuously improve the site's deviation management process (from A to Z)
Monitor key performance indicators to reduce overdue deviations and improve closure timelines
Strengthen the overall quality of deviation reports, including investigations, root cause analysis and CAPA robustness
Identify recurring deviations and drive initiatives to minimize reoccurrence and human‑error‑related causes
Operational Quality Leadership
Facilitate daily triage meetings to ensure proper deviation classification and efficient investigation launch
Lead or participate in boards/committees dedicated to deviation trends, CAPA review, and continuous improvement
Review and approve deviations of various criticality levels, ensuring compliance with quality and regulatory expectations
Provide coaching and guidance to investigators to help elevate investigation quality and consistency
Cross‑Functional Collaboration
Work closely with different internal teams to gather facts, support investigations, and align on process improvements
Ensure strong communication flows with internal quality stakeholders, fostering a culture of transparency and right‑first‑time execution.
Your Profile
To thrive in this role, you bring:
A Master's degree in Life Sciences, Engineering, Pharmacy, or an equivalent field
Proven experience in deviation management, quality assurance, or investigations within the pharmaceutical industry
Strong analytical mindset and excellent ability to drive Root Cause Analysis and CAPA processes
Solid organizational and leadership skills, with the ability to coach and challenge stakeholders constructively
Working knowledge of aseptic or controlled environments is a plus
Fluency in both English and French.
Our Recruitment Process
By applying for this position, you will go through the following steps:
Initial Screening – A first discussion with Olivia Braszko, Talent Acquisition Specialist
Technical Interview – A conversation with one of our technical experts to go trough technical aspects of the position and your background
Final Interview – A meeting with our Business Unit Director, Jimmy Rousseaux.
Interested? Apply Now
If you're driven by quality excellence and want to contribute to strengthening key pharmaceutical processes, we would be happy to meet you.
Send your CV to Olivia Braszko – Talent Acquisition Specialist at Nalys.
Let's build the future of life sciences together.
Brussels Area, Belgium
About Nalys
Nalys is a fast-growing consultancy company dedicated to delivering high‑value expertise across the life sciences and high‑tech engineering sectors. Our mission is to empower our consultants and partners by combining deep technical knowledge with a human‑centric approach. Joining Nalys means becoming part of a dynamic, supportive, and innovation‑driven community where your impact truly matters.
We are currently looking for a Deviations Management Expert to support one of our pharmaceutical partners located near Brussels. This role is an excellent opportunity for a quality professional eager to drive continuous improvement and strengthen deviation governance within a highly regulated environment.
Your Responsibilities
As a Deviations Management Expert, you will play a key role in ensuring robust deviation governance and enhancing process performance. Your main responsibilities include:
Deviation Process Governance & Performance
Oversee and continuously improve the site's deviation management process (from A to Z)
Monitor key performance indicators to reduce overdue deviations and improve closure timelines
Strengthen the overall quality of deviation reports, including investigations, root cause analysis and CAPA robustness
Identify recurring deviations and drive initiatives to minimize reoccurrence and human‑error‑related causes
Operational Quality Leadership
Facilitate daily triage meetings to ensure proper deviation classification and efficient investigation launch
Lead or participate in boards/committees dedicated to deviation trends, CAPA review, and continuous improvement
Review and approve deviations of various criticality levels, ensuring compliance with quality and regulatory expectations
Provide coaching and guidance to investigators to help elevate investigation quality and consistency
Cross‑Functional Collaboration
Work closely with different internal teams to gather facts, support investigations, and align on process improvements
Ensure strong communication flows with internal quality stakeholders, fostering a culture of transparency and right‑first‑time execution.
Your Profile
To thrive in this role, you bring:
A Master's degree in Life Sciences, Engineering, Pharmacy, or an equivalent field
Proven experience in deviation management, quality assurance, or investigations within the pharmaceutical industry
Strong analytical mindset and excellent ability to drive Root Cause Analysis and CAPA processes
Solid organizational and leadership skills, with the ability to coach and challenge stakeholders constructively
Working knowledge of aseptic or controlled environments is a plus
Fluency in both English and French.
Our Recruitment Process
By applying for this position, you will go through the following steps:
Initial Screening – A first discussion with Olivia Braszko, Talent Acquisition Specialist
Technical Interview – A conversation with one of our technical experts to go trough technical aspects of the position and your background
Final Interview – A meeting with our Business Unit Director, Jimmy Rousseaux.
Interested? Apply Now
If you're driven by quality excellence and want to contribute to strengthening key pharmaceutical processes, we would be happy to meet you.
Send your CV to Olivia Braszko – Talent Acquisition Specialist at Nalys.
Let's build the future of life sciences together.
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