Data Integrity&Validation Consultant (GxP), Breda
Data Integrity&Validation Consultant (GxP), Breda
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4800 Breda, Nederland
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Gewijzigd op: 1 week geleden
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Onthouden
Advertentietekst
Data Integrity&Validation Consultant (GxP) Location : Hybrid Type : Full-time
Are you passionate about
automation, analytical equipment, and data integrity in a regulated (GxP) environment ? Do you enjoy working where
quality, compliance, and technology
meet— and making sure systems and processes are not only working, but
audit-ready and future-proof ?
We are looking for a
Data Integrity&Validation Consultant (GxP)
who’s ready to support life sciences companies in building strong, compliant, and reliable processes across QC and production environments. In this role, you’ll apply
ALCOA+ principles , strengthen
data integrity governance , and support clients during
implementations, validations, audits, and inspections .
This position is ideal for someone who takes ownership, enjoys working across teams, and gets energy from solving complex quality and compliance challenges— while helping others grow along the way. If you’re ready to make an impact in the Life Sciences industry (and grow while doing it), we’d love to hear from you.
What’s in it for you? Make a real impact:
Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devices
Grow within a community of experts:
Benefit from knowledge-sharing, mentoring, and exposure to diverse assignments that broaden your expertise in automation, data integrity, and compliance.
Build a meaningful career: As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences.
A fair, competitive package:
We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations— because your contribution deserves to be valued.
What you bring
Act as a
Data Integrity (DI) specialist , monitoring and supporting compliance across QC and operational environments
Ensure
data integrity compliance during implementation of analytical equipment and automated systems
Apply and embed
ALCOA+ principles
across processes, systems, and ways of working
Bring advanced expertise on
data integrity expectations, standards, and best practices
within regulated environments
Identify DI risks and issues, create and own
Quality Risk Assessments , and ensure they lead to clear actions
Review outcomes of
quality audits and inspections
and support the development and execution of
corrective and preventive action plans (CAPA)
Support or lead
deviation management
related to data integrity and compliance topics
Consult on
new testing procedures and procedural changes , ensuring DI is built in from the start
Provide DI support during
equipment validations
(e.g., audit trail reviews/validation, system integrity checks)
Support DI guidance during
change control , ensuring validated and compliant status is maintained
Deploy and own
DI Gemba walks
and translate observations into sustainable improvements
Lead or support
data integrity governance processes
and help strengthen standard ways of working
Support
inspection readiness
and collaborate in internal and external audits
Coach, train, and guide colleagues and stakeholders to raise awareness and maturity around DI
Work according to
compliance best practices, EHSS requirements and lean principles
Perform other work-related activities assigned by your supervisor
Who you are Our culture is driven by values If this sounds like you, you’ll fit right in:
You’re
resilient
and tackle challenges with a positive mindset
You’re
curious
and always up for learning something new
You have a
no non-sense approach
honest, clear, respectful
You’re
innovative
and bring ideas, not just opinions
And above all, you’re
serious about your work, but not too serious about yourself
#J-18808-Ljbffr
Are you passionate about
automation, analytical equipment, and data integrity in a regulated (GxP) environment ? Do you enjoy working where
quality, compliance, and technology
meet— and making sure systems and processes are not only working, but
audit-ready and future-proof ?
We are looking for a
Data Integrity&Validation Consultant (GxP)
who’s ready to support life sciences companies in building strong, compliant, and reliable processes across QC and production environments. In this role, you’ll apply
ALCOA+ principles , strengthen
data integrity governance , and support clients during
implementations, validations, audits, and inspections .
This position is ideal for someone who takes ownership, enjoys working across teams, and gets energy from solving complex quality and compliance challenges— while helping others grow along the way. If you’re ready to make an impact in the Life Sciences industry (and grow while doing it), we’d love to hear from you.
What’s in it for you? Make a real impact:
Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devices
Grow within a community of experts:
Benefit from knowledge-sharing, mentoring, and exposure to diverse assignments that broaden your expertise in automation, data integrity, and compliance.
Build a meaningful career: As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences.
A fair, competitive package:
We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations— because your contribution deserves to be valued.
What you bring
Act as a
Data Integrity (DI) specialist , monitoring and supporting compliance across QC and operational environments
Ensure
data integrity compliance during implementation of analytical equipment and automated systems
Apply and embed
ALCOA+ principles
across processes, systems, and ways of working
Bring advanced expertise on
data integrity expectations, standards, and best practices
within regulated environments
Identify DI risks and issues, create and own
Quality Risk Assessments , and ensure they lead to clear actions
Review outcomes of
quality audits and inspections
and support the development and execution of
corrective and preventive action plans (CAPA)
Support or lead
deviation management
related to data integrity and compliance topics
Consult on
new testing procedures and procedural changes , ensuring DI is built in from the start
Provide DI support during
equipment validations
(e.g., audit trail reviews/validation, system integrity checks)
Support DI guidance during
change control , ensuring validated and compliant status is maintained
Deploy and own
DI Gemba walks
and translate observations into sustainable improvements
Lead or support
data integrity governance processes
and help strengthen standard ways of working
Support
inspection readiness
and collaborate in internal and external audits
Coach, train, and guide colleagues and stakeholders to raise awareness and maturity around DI
Work according to
compliance best practices, EHSS requirements and lean principles
Perform other work-related activities assigned by your supervisor
Who you are Our culture is driven by values If this sounds like you, you’ll fit right in:
You’re
resilient
and tackle challenges with a positive mindset
You’re
curious
and always up for learning something new
You have a
no non-sense approach
honest, clear, respectful
You’re
innovative
and bring ideas, not just opinions
And above all, you’re
serious about your work, but not too serious about yourself
#J-18808-Ljbffr
Belangrijke informatie
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BedrijfsnaamTRIUM Clinical Consulting NV
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PositieData Integrity&Validation Consultant (GxP)
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Meer informatie over deze advertentie
Data Integrity&Validation Consultant (GxP) is geplaatst in de Breda juridisch, consutancy rubriek op Locanto.
Op dit moment is dit de enige advertentie in deze rubriek onder Breda.
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