Commissioning & Qualification Equipment Engineer | Pharma | Beers

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.

Considering making an application for this job Check all the details in this job description, and then click on Apply.

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. xlxgzvr 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