QA Validation Engineer - Life Sciences (Flanders)

ALTEN Belgium is a leading consultancy company in the fields of Engineering, Life Sciences and IT in which our people and clients are central.

In our open and adaptable organization, we get the best out of our ambitious employees enabling them to perform optimally. We do this by offering them the most challenging projects, but also to continuously acquire new expertise to boost their careers. This can be done with the help of our ALTEN Academy, but also through our knowledge sharing events.

All employees together form a large network of expertise, even at an international level. In this way we offer optimal growth to our consultants and the best solutions for our customers.

Do you want to work in exciting projects at renowned clients? At ALTEN we believe that knowing and meeting the expectations of our consultants is a key factor in our success. Our consultants make the difference. Do you want to make the difference too?

We are currently looking for a QA Validation Engineer to join our team.

As a QA Validation Engineer, you'll support the QA Engineering department in assuring that all Qualification/Validation-related regulatory and procedural requirements are fulfilled during the complete life cycle (concept, project, operational and retirement phase).

Multiple profiles are required and, based on the provided profile, a match will be made with one or more of the following specific sub-topics:

• Manufacturing Systems Qualification
• Laboratory Systems Qualification
• Facility and Utility Systems Qualification
• IT / Automation Systems
• Computer System Validation

Main responsibilities:

Review and approve qualification/validation documents and quality records such as: SOPs, User Requirements, Impact / Risk Analyses, Test Plans, Test Scripts, Change Controls, CAPAs, Maintain compliance with regulations, guidelines, and the company's policies and standards.

• Be part of engineering teams and interact with other groups for the introduction of new or upgraded systems and processes.
• Provide advice and support for the preparation of qualification/validation-related activities and safeguard cGMP aspects.
• Address and follow up on deviations occurring during the execution of qualification/validation activities.
• Communicate status (quality & compliance, planning, etc.) to QA qualification/validation team members.

Your profile:

Knowledge & Experience:

• Experience in the chemical and/or pharmaceutical industry with respect to qualification/validation.
• Knowledge of cGMP regulations and guidelines.

Skills & Competencies:

• Ability to translate technical information into content understandable at all levels of the organization.
• Ability to correctly estimate urgency, criticality, and impact of decisions related to the function.
• Ability to multi-task and work on a variety of projects simultaneously.
• Ability to work independently and in a cross-functional team environment.
• Strong communication skills.

Languages:

• Fluent in English and Dutch (written and spoken).

Specific Know-How:

• Systems: Manufacturing, Laboratory, Building, Utility, IT, Automation systems used within the pharmaceutical or chemical industry
• Problem reporting and change request systems (e.g. TrackWise, Comet)
• Document Management Systems (e.g. TruVault)
• Test tools (e.g. Kneat)

What ALTEN has to offer

• A permanent contract
• A salary package in line with your experience and extra benefits (company car, meal vouchers, recovery days, insurances)
• The possibility to join a great team and be part of the success story of an international group

We are also open to work with freelancers!

Apply now and be a part of our amazing journey. We believe in growing together!

We are looking forward to getting to know you and your ambitions!