Quality Senior Engineer (Johnson & Johnson)
Randstad
- Courcelles, Hainaut
- CDD
- Temps-plein
Within the role, you will be responsible for the following processes:
o QA Zone Owner: VAS area ...The "VAS area," where VAS stands for Value Added Services, is the dedicated space within the Distribution Center where all the repack and relabel activities take place. This is the hub of transformative actions where products undergo packaging modifications, labeling updates, or other value-enhancing processes to meet specific customer requirements, regulatory compliance, or marketing needs. In the VAS area, highly skilled and meticulous professionals work diligently to ensure precise execution of repackaging and relabeling tasks, guaranteeing the integrity, safety, and marketability of the medical devices. This dynamic space operates as a critical link between the manufacturing process and the final delivery to customers, adding value by customizing products and
aligning them with unique market demands.
o QMS SME: Change controlAs a member of our team, you will be accountable:
o Deliver for Patients and Customer
o Change control process
o Drive a culture of continuous improvement
o Audit readiness and certification
o Strengthen the compliance of the site by effective change control management and assuring new changes are optimally, timely and compliantly implemented. Evaluate and ensure accurate documentation of applicable quality records and approve accordingly.
o Get encouraged and activated by supporting project team activities and guiding them towards compliant project execution.
o Broaden your network by the involvement in all Med Tech portfolio. Collaborate with peers in other parts of the EMEA commercial quality organization to improve process excellence, simplification, and standardization across distribution sites.
toon meerJ&J Med Tech is recruiting for a Quality Senior Engineer to be located in Courcelles, Belgium.Key Responsibilities:
Within the role, you will be responsible for the following processes:
o QA Zone Owner: VAS area
The "VAS area," where VAS stands for Value Added Services, is the dedicated space within the Distribution Center where all the repack and relabel activities take place. This is the hub of transformative actions where products undergo packaging modifications, labeling updates, or other value-enhancing processes to meet specific customer requirements, regulatory compliance, or marketing needs. In the VAS area, highly skilled and meticulous professionals work diligently to ensure precise execution of repackaging and relabeling tasks, guaranteeing the integrity, safety, and marketability of the medical devices. This dynamic space operates as a critical link between the manufacturing process and the final delivery to customers, adding value by customizing products and
aligning them with unique market demands.
o QMS SME: Change controlAs a member of our team, you will be accountable:
o Deliver for Patients and Customer
o Change control process ...o Drive a culture of continuous improvement
o Audit readiness and certification
o Strengthen the compliance of the site by effective change control management and assuring new changes are optimally, timely and compliantly implemented. Evaluate and ensure accurate documentation of applicable quality records and approve accordingly.
o Get encouraged and activated by supporting project team activities and guiding them towards compliant project execution.
o Broaden your network by the involvement in all Med Tech portfolio. Collaborate with peers in other parts of the EMEA commercial quality organization to improve process excellence, simplification, and standardization across distribution sites.
toon meerervaringjouw aanbodQualifications:
A minimum of a Bachelor's degree in Science, Engineering or other technical field is required. A Master of Science or in Engineer degree is preferred.Experience and Skills required:
o 4-7 years QA related experience within an operational pharmaceutical or Medical Devices environment
o Good knowledge in QMS system process (document management, change control, non-conformance, CAPA, standards assessments)
o Knowledge of GMP/GDP/ISO 13485 regulations
o Fluent in French & English
o Ability to prioritize tasks and work independently
o Embedded in shopfloor activities
o Pragmatic
o Problem-solving skills
o Good communication
o Agility invested in good collaborations with multiple partners, focus to details
o Experience with digital solutions such as EtQ, Trackwise, Qlik, SAP for the management of Quality Systems against on the basis of disabilityopleiding
- Professionele bachelor
- Academische bachelor
- Master
The position is based within European Distribution Center at Courcelles, allowing to be exposed to the operational environment and responsible for QA operational activities such as shop-floor investigation & inspections and continuous improvement. Every team member acts as a single point of contact for an operational area (QA Zone owner) and supports the area for all quality related topics (eg. Gemba-walk, CAPA, auditing, ..). As Quality team, we develop and deploy effective and efficient quality processes that meet customer needs and applicable J&J & Health Authority compliance requirements to support our growth.werken bij gmed healthcareGMED HEALTHCAREwerklocatieRue du Luxembourg, 5 6180 Courcelles, HenegouwenJohnson & Johnson is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related products for the consumer, pharmaceutical and professional markets.Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age,...national origin, or protected veteran status and will not be discriminated against on the basis of disability.toon mindertoon meerJohnson & Johnson is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related products for the consumer, pharmaceutical and professional markets.Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.sollicitatieprocedure.Benieuwd hoe het sollicitatieproces loopt? Ontdek hier hoe wij je helpen om de job binnen te halen.1 van 5solliciteren is heel eenvoudig.Klik op de 'solliciteer nu'-knop, maak je profiel aan en motiveer waarom jij de beste kandidaat bent voor deze job. Tip: hou je profiel up-to-date, zodat je altijd snel kan solliciteren.2 van 5je ontvangt een bevestigingsmail.Zo weet je dat wij met je sollicitatie aan de slag gaan. Heel concreet bekijken we of jouw profiel beantwoordt aan de eisen van de job.3 van 5je komt in aanmerking!Dan nemen we contact op. We overlopen samen je cv en de verdere stappen van je sollicitatie (gesprek, testing, referenties, rondleiding, ...).4 van 5we bespreken je cv met onze klant.We maken hem duidelijk waarom jij de geknipte kandidaat bent. Zodra hij zijn feedback geeft - dat kan soms enkele dagen duren - brengen we je op de hoogte.5 van 5is het bedrijf enthousiast?…en ben jij dat ook nog altijd? Dan kan je het contract tekenen en is het tijd voor een feestje!contacteer ons.voor al je vragen neem contact op met.IOisabeau ostvacatures in je mailbox.Makkelijk gepaste jobs ontvangen in jouw mailbox? Wanneer jij wilt? Dat kan met de Randstad jobagent!e-mailadres*frequentieIk ga akkoord met het gebruik van mijn gegevens voor het versturen van jobagents. verzendenJob alert succesvol aangemaakt.je motivatiesolliciteercontracttypecontracttypejobs per sectorjobs per sectorcontacteer onscontacteer onsmy Randstadmy Randstadvoor werkgeversvoor werkgeversRandstad Belgium nv (BE0402.725.291), Randstad Construct nv (BE0438.801.472), allen gevestigd in Access Building, Keizer Karellaan, 586 bus 8 te 1082 Brussel