Commissioning & Qualification Equipment Engineer | Pharma | Beers

Belgie Vacature; Beerse; On-site; EUR 70,000 - 100,000; Full time

Benefits offered by this job

Electric company car

Meal vouchers

Eco vouchers

Expense allowance

Group insurance

Hospitalization insurance

12 extra leave days (ADV)

Job summary

Select Projects in Belgium is seeking a Commissioning & Qualification Equipment Engineer to prepare, maintain and execute qualification documentation for GMP-critical equipment, utilities and systems. You’ll ensure documentation meets GMP and internal quality standards while collaborating with C&Q leads and project teams.

You’ll participate in qualification testing, support audits, and help keep systems validated and compliant.

Qualifications

• Bachelor's or Master's degree in a scientific or technical field.
• Strong interest in GMP-regulated environments.
• Excellent technical writing and documentation skills.
• Experience with engineering systems, utilities or manufacturing equipment is an asset.
• Fluent in Dutch and English, both written and spoken.

Responsibilities

• Write qualification documentation including URS, SRS, IA, DQ, IQ, OQ, PQ, QSR and Validation Master Plans.
• Execute and document qualification tests for equipment, utilities and systems.
• Assess the impact of changes, deviations and discrepancies on qualification activities.
• Coordinate document reviews, approval flows and signature processes.
• Follow up punch list items and qualification actions until closure.
• Supporting internal and external audits and inspections.
• Managing document archiving in accordance with GMP and GDP requirements.

Skills

Dutch fluency

English fluency

Technical writing

Education

Bachelor's or Master's degree in a scientific/technical field (Industrial Engineering, Biochemistry, Biotechnology or Pharmaceutical Sciences)

Job description

Taken en verantwoordelijkheden

At Select Projects, the experience our clients have with our consultants is what matters most. Our consultants create that experience by delivering the highest quality in everything they do. Your expertise is central to this, and at Select Projects you will have the opportunity to keep growing so you can become and deliver the best version of yourself.

As a consultant, you bring knowledge, skills and the drive to succeed. What do you get in return?

Select Projects offers technically challenging projects, career growth opportunities, autonomy, trust, training and knowledgeable colleagues who are happy to share their expertise. This allows you to continuously develop both professionally and personally.

At Select Projects, you are not only part of the client's team. Together with your fellow consultants in the field, you are also part of our team. We value a family-oriented culture where people genuinely help and support each other. This enables you to become and deliver the best version of yourself. Working at Select Projects means continuously developing your craftsmanship and becoming a true specialist in your field.

As a Commissioning & Qualification Equipment Engineer, you are responsible for preparing, maintaining and executing qualification documentation for GMP-critical equipment, utilities and systems. You ensure that all documentation complies with applicable GMP requirements and internal quality standards. You work closely with C&Q Leads, Subject Matter Experts and project teams to support qualification projects from initiation through completion. Besides document preparation, you also participate in qualification testing and follow-up activities. Your work plays an important role in ensuring that systems remain in a validated and compliant state.

Fortunately, We Can Count On You For

• Writing qualification documentation including URS, SRS, IA, DQ, IQ, OQ, PQ, QSR and Validation Master Plans
• Executing and documenting qualification tests for equipment, utilities and systems
• Assessing the impact of changes, deviations and discrepancies on qualification activities
• Coordinating document reviews, approval flows and signature processes
• Following up punch list items and qualification actions until closure
• Supporting internal and external audits and inspections
• Managing document archiving in accordance with GMP and GDP requirements

Profiel kandidaat

You are structured, quality-minded and eager to learn. You communicate effectively with different stakeholders and enjoy working in a team-oriented GMP environment. At the same time, you are capable of independently managing documentation and qualification activities.

What you bring

• Bachelor's or Master's degree in a scientific or technical field such as Industrial Engineering, Biochemistry, Biotechnology or Pharmaceutical Sciences
• Strong interest in the pharmaceutical industry and GMP-regulated environments
• Excellent technical writing and documentation skills
• Experience with engineering systems, utilities or manufacturing equipment is an asset
• Fluent in Dutch and English, both written and spoken

Geboden wordt

At Select Projects, we make sure you join a pleasant working environment where great colleagues and team spirit are at the heart of everything we do. We regularly organize after-work events, company parties, sports activities and team-building initiatives.

We also offer plenty of opportunities for you to grow and develop. Together, we create a personalized training plan tailored to your ambitions, future goals and development needs. At Select Projects, you can become and deliver the best version of yourself.

In addition, Select Projects offers you a permanent contract with an attractive salary package, including the following benefits:

• Electric company car with charging card
• Meal vouchers & eco vouchers
• Expense allowance
• Group insurance & hospitalization insurance
• 12 additional leave days (ADV) per year
• End-of-year bonus
• Single and double holiday pay
• Bonus system including both collective and individual bonuses
• Opportunity to participate in the Flex Income Plan program