Project Engineer - (GxP Environment)

Project Engineer - (GxP Environment); Diegem; On-site; EUR 60,000 - 90,000; Full time

Benefits offered by this job

Mobility options (incl. company car)

Insurance coverage

Meal vouchers

Eco-cheques

Sopra Steria Academy

Team events

Job summary

Sopra Steria is seeking a Project Engineer to ensure GxP systems meet regulatory requirements throughout the lifecycle. You will drive specification, procurement, installation, validation and handover, while coordinating with multidisciplinary teams and suppliers.

A strong focus on quality, compliance and continuous improvement is required. Ideal candidates hold a Master’s degree in engineering or science and have GMP experience, with excellent organizational and communication skills.

Qualifications

• Master’s degree in a technical or scientific field.
• Experience in pharmaceutical and/or GMP environment is a strong asset.
• Knowledge of validation processes and sterile production is a plus.
• Strong organizational and communication skills.
• Ability to work independently and take initiative.
• Team player with analytical thinking skills.
• Flexibility and resilience in dynamic projects.
• Experience in project coordination and contractor management is a plus.
• Proficiency in English; Dutch is a plus.

Responsibilities

• Oversee the full project lifecycle: from specification and procurement to installation, validation and handover to operations.
• Collaborate in multidisciplinary teams and monitor planning and budget.
• Ensure safe, compliant and efficient execution and quality throughout.
• Provide technical follow-up with suppliers and communicate with stakeholders.

Skills

Organizational skills

Communication skills

Initiative

Team player

Analytical thinking

Education

Master’s degree in engineering or science

Job description

Company Description

Sopra Steria offers tailored, end-to-end corporate technology and software solutions to help clients make bold choices and deliver results. Successfully so! With more than51.000 colleagues in 30 countries, we rank as Europe’s leading digital solutions provider. Some of the most successful companies in Europe rely on our technology due to our commitment to innovation, collaboration, and value in business development.

The world is how we shape it. Let’s shape it together.

Job Description

As a quality and compliance expert, you will be responsible for ensuring that GxP systems and processes adhere to the applicable regulatory requirements throughout the entire system lifecycle. Therefore, you stay up to date about evolving regulations from authorities such as the EMA and FDA and industry standards like GAMP and ISO. Depending on your role and expertise, you may be asked to provide Quality & Compliance support during audits and inspections, or to join a Sopra Steria validation service team.

Are you a technically skilled engineer with a passion for pharmaceutical processes? As a Project Engineer, you will contribute to various engineering projects. You’ll be responsible for the full project lifecycle of specific installations or equipment: from specification and procurement to installation, validation, and handover to operations. You’ll work in multidisciplinary teams, monitor planning and budget, and ensure safe, compliant, and efficient execution. You’ll also be part of creating technical solutions and be included in the technical follow-up with suppliers. You take ownership of your scope, communicate proactively with stakeholders, and contribute to continuous improvement.

Qualifications

We’re seeking passionate colleagues who are eager to push the boundaries in digital transformation and technology consulting. At Sopra Steria, you’ll have the opportunity to grow your skills in a constructive, collaborative team environment, working on impactful projects that drive change for our clients. If you thrive on challenge and meet (most of) the qualifications below, we look forward to your application!

• Master’s degree in a technical or scientific field (industrial, civil, or bio-engineering)
• Experience in a pharmaceutical and/or GMP environment is a strong asset
• Knowledge of validation processes and sterile production is a plus
• Strong organizational and communication skills
• Ability to work independently and take initiative
• Team player with analytical thinking skills
• Affinity with technical, technological, and process-related aspects
• Flexible and resilient in a dynamic project environment
• Experience in project coordination and contractor management is a plus
• Good command of English is required and Dutch is a plus

Additional Information

Are you ready to further develop your career? Then we'd love to point you in the right direction. With offices in more than 30 countries, that direction might lead you to places you've never been to before. Would you prefer to grow internally? That's possible, too. We challenge you to keep pushing yourself to become the best you can be.

We offer a generous employee benefits package that includes:

• A variety of perks, such as mobility options (including a company car), insurance coverage, meal vouchers, eco-cheques, and more.
• Continuous learning opportunities through the Sopra Steria Academy to support your career development.
• The opportunity to connect with fellow Sopra Steria colleagues at various team events.

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Sopra Steria is an equal opportunity employer. All qualified applicants will be considered for employment without regard to age, ancestry, nationality, color, family or medical leave, gender identity or expression, genetic information, immigration status, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran or military status, race, ethnicity, religion, gender (including pregnancy), sexual orientation or any other characteristic protected by applicable local laws, regulations and ordinances. We foster a work environment that is inclusive and respectful of all differences.