Join a leading organization where your expertise in
Project Engineering
will play a crucial role in the successful execution of capital projects. You will be part of a dynamic environment that advances high-quality standards and compliance in the pharmaceutical industry.
As the ideal candidate, you are a skilled
Project Engineer
adept at coordinating and managing intricate validation and planning activities. If you are passionate about ensuring quality standards and enjoy collaborating with cross-functional teams, this opportunity is tailored for you.
* You coordinate the validation and planning activities for capital projects.
* You manage project scheduling and execution to ensure alignment with business objectives.
* You interpret and apply GMP regulations and international standards effectively.
* You act as the main contact for Engineering and Quality Assurance regarding validation and change control.
* You facilitate Quality Risk Assessments and provide expertise in verification and validation.
* You conduct urgent quality investigations and implement necessary changes.
* You contribute to the qualification and validation of method improvements within laboratory contexts.
What are we looking for?
* You hold a
Master's degree
in civil, industrial, bio-engineering, industrial pharmacy, or related scientific fields.
* You have
3-5 years of experience
in production environments, preferably within the pharmaceutical industry.
* You are experienced in aseptic processes, cleaning, disinfection, and sterilization.
* You have strong communication and stakeholder management skills.
* You are detail-oriented and exhibit strong organizational abilities.
* You have technical writing skills that enable you to draft and review validation documents with precision.
* You are proficient in
Dutch
and
English
.