Senior Pharma Process Engineer — cGMP & Leadership

polytek

Beringen, Tienen

On-site

EUR 90,000 - 120,000

Full time

4 days ago
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Job summary

Polytek in Belgium (Tienen and Beringen) is seeking an experienced Process Engineer to design, optimise and safeguard pharmaceutical and biotech processes, ensuring compliance, safety and cost efficiency. You will lead technical workstreams, mentor junior engineers, coordinate with QA, suppliers and BIM modelers, and ensure cGMP adherence across projects.

Applicants have a Master in relevant field and 8–10 years' experience, fluent in English and Dutch, and a drive to deliver high-quality

Qualifications

  • Master's degree in (Bio)Chemical, Process, Pharmaceutical or Industrial Engineering.
  • 8–10 years of relevant process engineering experience.
  • Proven track record in pharmaceutical/biotech industries.
  • Experience in senior or lead engineering roles.
  • Knowledge of cGMP and EU/FDA regulatory standards.
  • Familiar with IQ/OQ/PQ lifecycle and ISO cleanroom standards.
  • Proficiency with MS 365 and process simulation tools.
  • Strong English and Dutch language skills.

Responsibilities

  • Analyse stakeholder and client requirements into technical process solutions.
  • Design and optimise pharmaceutical processes focusing on efficiency, safety and regulatory compliance.
  • Coordinate with project teams, suppliers and BIM Modelers to integrate process designs.
  • Coach and mentor junior engineers and provide technical leadership.
  • Act as technical point of contact for key pharmaceutical clients.
  • Identify opportunities and contribute to proposals and tenders.

Skills

Process engineering
Leadership
Regulatory compliance
Client coordination

Education

Master's in chemical/biomedical/industrial engineering

Tools

MS 365
FluidFlow

Job description

Polytek in Belgium (Tienen and Beringen) is seeking an experienced Process Engineer to design, optimise and safeguard pharmaceutical and biotech processes, ensuring compliance, safety and cost efficiency. You will lead technical workstreams, mentor junior engineers, coordinate with QA, suppliers and BIM modelers, and ensure cGMP adherence across projects.

Applicants have a Master in relevant field and 8–10 years' experience, fluent in English and Dutch, and a drive to deliver high-quality

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