Csv Engineer

Oltera PG; Geel; On-site; EUR 36,000 - 43,000; Full time

Benefits offered by this job

Company car

Meal vouchers

Eco vouchers

Home-working allowance

Mobile phone allowance

Hospitalisation insurance

Group insurance

Job summary

Oltera PG is looking for a CSV Engineer to join a Geel-based project supporting a pharmaceutical company. Juniors are encouraged to apply, with hybrid options depending on project phase. The role welcomes employees and freelancers/contractors and includes a broad benefits package.

The position emphasizes clear validation planning, regulatory alignment, and hands-on testing to ensure data integrity and audit readiness. Strong English is required; Dutch is a plus.

Qualifications

• Bachelor’s or Master’s degree in (Bio)Engineering, Computer Science, Chemistry, or similar.
• Curious, thorough, and ready to take ownership of validation tasks.
• Interest in software validation and pharmaceutical regulations (basic knowledge of GMP, GAMP 5, 21 CFR Part 11 is a plus).
• Strong English communication skills; Dutch is an advantage but not required.

Responsibilities

• Prepare clear, usable validation plans and IQ / OQ / PQ protocols.
• Execute tests to verify system functionality, data integrity, and regulatory compliance.
• Translate client needs into documented validation requirements and validation reports.
• Collaborate with project teams and the client in Geel to keep validation on-time and audit-ready.
• Support audits and regulatory inspections with calm, evidence-backed answers.

Skills

Curious

Ownership

Junior-friendly

Education

Bachelor’s or Master’s degree in (Bio)Engineering, Computer Science, Chemistry, or similar

Job description

Do you enjoy turning rules into reliable results? Join our client as a CSV Engineer for a client project in Geel supporting a pharmaceutical company. We’re serious about qualityand fully committed to helping you grow — juniors encouraged. Freelancers welcome.

What you’ll actually do

• Prepare clear, usable validation plans and IQ / OQ / PQ protocols.
• Execute tests to verify system functionality, data integrity, and regulatory compliance.
• Translate client needs into documented validation requirements and validation reports.
• Collaborate with project teams and the client in Geel to keep validation on-time and audit-ready.
• Support audits and regulatory inspections with calm, evidence-backed answers.

Who we’re looking for

• Bachelor’s or Master’s degree in (Bio)Engineering, Computer Science, Chemistry, or similar.
• Curious, thorough, and ready to take ownership of validation tasks. Junior profiles encouraged to apply.
• Interest in software validation and pharmaceutical regulations (basic knowledge of GMP, GAMP 5, 21 CFR Part 11 is a plus).
• Strong English communication skills; Dutch is an advantage but not required.
• Availability to work on-site in Geel as required (hybrid options may apply depending on project phase).
• Open to applications from employees and freelancers/contractors — please state your preferred engagement type and availability.
• Starting gross monthly salary of at least €3,500 for junior employees (actual offer for mid/senior hires will be competitive and commensurate with experience).
• Company car and fuel card (employee roles, eligibility per policy).
• Meal vouchers and eco vouchers.
• Home-working allowance and mobile phone allowance.
• Hospitalisation insurance and group insurance (employee benefits).
• Hybrid working options depending on project needs; this vacancy supports an on-site project in Geel.
• Freelancers: competitive day rates and flexible contracting arrangements.

HR & legal

• Right to work: Offers are subject to verification of the legal right to work in the relevant country; candidates must provide documentation upon request.
• Background checks: Final offers may be conditional on satisfactory background checks, references, and other pre-employment screening as permitted by local law.
• Data privacy: Applicant personal data will be processed for recruitment purposes in accordance with our privacy policy. By applying, you consent to recruitment-related processing of your personal data.
• Reasonable accommodations: If you require adjustments to participate in the recruitment process, please contact us — we will make reasonable accommodations consistent with applicable law.