C&Q Engineer
Il y a 4 heures
Beerse, Flanders, Belgique
Panda International
Temps plein
Gratuit avec email ou Google
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Gratuit avec email ou Google
C&Q Engineer – Pharmaceutical Manufacturing – Belgium
Job Description
A leading global pharmaceutical organization is looking for an experienced Commissioning & Qualification (C&Q) Engineer to join their engineering team in Beerse, Belgium. The role is part of a large-scale pharmaceutical manufacturing environment focused on ensuring that critical equipment and systems remain compliant, qualified, and ready to support the production of life-saving medicines. As a C&Q Engineer, you will act as a subject matter expert for Equipment Commissioning & Qualification, working closely with Engineering, Operations, Quality, and Maintenance teams. You will play a key role in maintaining the qualified state of equipment throughout its lifecycle and supporting continuous improvement initiatives.
Key Responsibilities
- Act as a C&Q subject matter expert for equipment qualification activities
- Develop, execute, and maintain commissioning and qualification strategies
- Ensure equipment remains in a validated and compliant state throughout its lifecycle
- Collaborate with Engineering, Operations, Quality, and Maintenance departments
- Represent C&Q during regulatory and client quality audits
- Communicate qualification strategies, progress, and status to stakeholders
- Drive improvements in QMS, C&Q processes, methodologies, and tools
- Provide guidance and mentorship to external C&Q engineers Required Experience & Skills
- Extensive experience in Commissioning & Qualification (C&Q) within a GMP environment
- Strong knowledge of GMP regulations, including Annex 1 and 21 CFR Part 11
- Proven experience with qualification of:
- Equipment
- Production systems
- Utilities
- Facilities
- Ability to work both strategically and hands-on in a complex pharmaceutical environment
- Strong understanding of compliance, quality systems, and risk-based qualification approaches
- Excellent communication skills with the ability to engage stakeholders at different organizational levels Ideal Candidate Profile
- Strong hands-on mentality with a passion for C&Q engineering and compliance
- Team player who enjoys collaboration and sharing expertise
- Quality and safety-focused mindset
- Strong interpersonal and communication skills
- Master’s degree in Engineering, Science, or equivalent experience
- Professional English language skills required
- Dutch language skills are highly preferred Project Context The site is currently undergoing a major equipment revamp and requalification program, with significant investment planned to support future manufacturing capabilities. This is an excellent opportunity for an experienced C&Q Engineer to contribute to a high-impact pharmaceutical project within an international environment.
Job Description
A leading global pharmaceutical organization is looking for an experienced Commissioning & Qualification (C&Q) Engineer to join their engineering team in Beerse, Belgium. The role is part of a large-scale pharmaceutical manufacturing environment focused on ensuring that critical equipment and systems remain compliant, qualified, and ready to support the production of life-saving medicines. As a C&Q Engineer, you will act as a subject matter expert for Equipment Commissioning & Qualification, working closely with Engineering, Operations, Quality, and Maintenance teams. You will play a key role in maintaining the qualified state of equipment throughout its lifecycle and supporting continuous improvement initiatives.
Key Responsibilities
- Act as a C&Q subject matter expert for equipment qualification activities
- Develop, execute, and maintain commissioning and qualification strategies
- Ensure equipment remains in a validated and compliant state throughout its lifecycle
- Collaborate with Engineering, Operations, Quality, and Maintenance departments
- Represent C&Q during regulatory and client quality audits
- Communicate qualification strategies, progress, and status to stakeholders
- Drive improvements in QMS, C&Q processes, methodologies, and tools
- Provide guidance and mentorship to external C&Q engineers Required Experience & Skills
- Extensive experience in Commissioning & Qualification (C&Q) within a GMP environment
- Strong knowledge of GMP regulations, including Annex 1 and 21 CFR Part 11
- Proven experience with qualification of:
- Equipment
- Production systems
- Utilities
- Facilities
- Ability to work both strategically and hands-on in a complex pharmaceutical environment
- Strong understanding of compliance, quality systems, and risk-based qualification approaches
- Excellent communication skills with the ability to engage stakeholders at different organizational levels Ideal Candidate Profile
- Strong hands-on mentality with a passion for C&Q engineering and compliance
- Team player who enjoys collaboration and sharing expertise
- Quality and safety-focused mindset
- Strong interpersonal and communication skills
- Master’s degree in Engineering, Science, or equivalent experience
- Professional English language skills required
- Dutch language skills are highly preferred Project Context The site is currently undergoing a major equipment revamp and requalification program, with significant investment planned to support future manufacturing capabilities. This is an excellent opportunity for an experienced C&Q Engineer to contribute to a high-impact pharmaceutical project within an international environment.