13 beste vacatures voor de functie van qa in lokeren eksaarde (nieuwe medewerkers gezocht)

Quality Lead (Turnover)
PM Group —Gent
- Master
- Bouw
- Ter plaatse
OT Quality Associate
Novartis —Puurs
- € 61.300 - € 113.900 per jaar
- Voltijds
- Engels
- Master
- Projectmanagement
- Pensioensparen
3 dagen
Quality Specialist
ALDI —Erpe-Mere
- Microsoft Excel
- Engels
- Bachelor
- Thuiswerkopties
- Pensioensparen
Specialist, Quality Control I
Novartis —Puurs
- € 42.700 - € 79.300 per jaar
- Voltijds
- Analytisch vermogen
- Bachelor
- Ter plaatse
- Verhuiskostenvergoeding
3 dagen
Teammanager QA Food (Oost-Vlaanderen)
Normec Foodcare BE —Gent
- Weekendbeschikbaarheid
- Hybride werken
- Engels
- Bachelor
- Organisatorische vaardigheden
Snel solliciteren
QA Engineer- Puurs, BE
Purna Pharmaceuticals nv —Puurs
- Voltijds
- Engels
- Master
- Bachelor
Snel solliciteren
Quality Technician
AMETEK, Inc. —Zele
- € 20.000 - € 25.000 per jaar
- Voltijds
- Productie
- Pensioensparen
QA Engineer Logistics
Alcon —Bornem
- Voltijds
- Communicatieve vaardigheden
AD Lab technician (dagploeg)
Ajinomoto Bio-Pharma Services —Wetteren
- Analytisch vermogen
- Bachelor
Quality Control Analyst- Puurs, BE
Purna Pharmaceuticals nv —Puurs
- Voltijds
- Analytisch vermogen
- Bachelor
Snel solliciteren
CPK QA Controller
Alcon —Puurs
- Voltijds
QA Lead Upstream
Barry Callebaut —Lebbeke Wieze
2 dagen
QUALITY ENGINEER
Anglo Belgian Corporation —Gent
- Bachelor

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Quality Lead (Turnover)

PM Group -
Gent

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Vacaturegegevens

Vaste Jobs

Kwalificaties

Frans
Master
Kwaliteitsborging
Cleanroom
Bouw

Volledige vacaturetekst

PM Group are seeking an experienced Quality Lead (Turnover) to oversee all site quality matters, with primary focus on Turnover activities for a major pharmaceutical construction project in Ghent, Belgium. This critical role requires a seasoned professional to establish and maintain the highest quality standards throughout the construction and commissioning phases of a state-of-the-art pharmaceutical manufacturing facility.

The successful candidate will be responsible for implementing comprehensive quality management systems, ensuring GMP compliance, and managing all quality-related activities from construction through to facility handover and validation.

Managing Project Completions for multiple systems
Approval of Vendor Turnover Packages (VTOPs)
Approval of Trade Turnover Packages (TTOPs)
Coordination of Trade Walkdowns
Punchlist Management and closeout
Managing Engineering Document Control
Transfer of VTOPs & TTOPs to Operations
Receipt, review and acceptance of As Built Drawings
Management of Non GMP Change Controls
Auditing of the following groups to ISO and project standards:
- Construction Management Team
- Construction Contractors
- Suppliers and Vendors
Metrics tracking and reporting in relation to Completions, Turnover and Quality
Provide expertise and guidance in relation to construction QA for all construction activities onsite
Establish a ‘Right First Time’ culture onsite.
Ensure all construction activities comply with Good Manufacturing Practice requirements and regulatory standards
Direct daily quality activities across all construction disciplines and contractors
Oversee quality documentation, IQ/OQ protocols, and validation master plans
Coordinate internal and external quality audits, regulatory inspections, and client assessments
Lead investigation and resolution of quality issues and deviations
Monitor subcontractor quality performance and compliance with project specifications
Deliver quality training programs for project teams and contractors

Degree in Engineering, Science, Quality Management, or related discipline
Minimum 8+ years in quality management roles on major construction / engineering projects
Proven experience in pharma facility construction quality management
Deep understanding of GMP, and Belgian/EU pharmaceutical regulations
Extensive experience with ISO 9001, quality management systems, and validation processes
Fluent English essential; Dutch/French advantageous
Qualified internal auditor with experience managing regulatory inspections
Professional quality qualification advantageous
Experience with cleanroom construction and controlled environment validation advantageous
Understanding of pharmaceutical engineering standards

D&I

Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future.

PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know.

For more company information visit our company website > Meet Our Team - careers | PM Group

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qa vacatures in lokeren eksaarde

Quality Lead (Turnover)

OT Quality Associate

Quality Specialist

Specialist, Quality Control I

Teammanager QA Food (Oost-Vlaanderen)

QA Engineer- Puurs, BE

Quality Technician

QA Engineer Logistics

AD Lab technician (dagploeg)

Quality Control Analyst- Puurs, BE

CPK QA Controller

QA Lead Upstream

QUALITY ENGINEER

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