Quality Engineer Vast Contract – Regio Gent #QualityAssurance #ContinuousImprovement #SupplierManagement
Ben jij een kwaliteitsgedreven professional met oog voor detail en passie voor verbetering? Werk je graag in een technische omgeving waar kwaliteit en innovatie hand in hand gaan? Dan hebben wij een uitdagend project dat perfect bij jou past!
Voor een sterke en internationale speler zijn we op zoek naar een Quality Engineer (m/v/x) die mee wil bouwen aan de kwaliteitscultuur binnen complexe (nucleaire) projecten. Klaar om samen met Jefferson Wells aan de slag te gaan? Lees dan zeker verder!
Jouw verantwoordelijkheden? Als Quality Engineer ben je verantwoordelijk voor het waarborgen van de kwaliteitsnormen binnen de volledige supply chain en ondersteun je diverse afdelingen in hun streven naar continue verbetering. Je takenpakket omvat:
De kwaliteitsopvolging bij leveranciers en ondersteuning van het aankoopteam bij de validatie van nieuwe leveranciers
Het opvolgen van kritische activiteiten binnen nucleaire projecten en deelnemen aan kwaliteitsaudits
Actieve probleemoplossing bij kwaliteitsissues en het opstarten van verbetertrajecten
Beheer van non-conformiteiten, inclusief root cause analyses, actieplannen en borging van verbeteringen
De opvolging en controle van certificaten en kwaliteitsdocumenten
Ondersteuning bij externe audits (ISO 9001, klantaudits, nucleaire audits) en kwaliteitsprojecten
Wie ben je? Je bent een communicatief sterke teamplayer die vlot samenwerkt en graag initiatief neemt. Met een bachelorsdiploma en een eerste ervaring binnen een technische of projectomgeving beschik je over de nodige basis om kwaliteitsverbeteringen te realiseren. Je werkt vlot met MS Office en hebt een sterke interesse in techniek – affiniteit met motoren versterkt je kandidatuur.
Wat kan je verwachten? Jefferson Wells biedt jou een dynamische werkomgeving waar kwaliteit en innovatie centraal staan. Je mag rekenen op een grondig opleidingstraject, een competitief loonpakket met extra legale voordelen, en de kans om te groeien binnen een onderneming waar samenwerking en expertise centraal staan. Voldoe jij aan dit profiel en ben je klaar voor de volgende stap in je carrière?
Solliciteer dan rechtstreeks via de website of contacteer Sara Van den Bossche op het nummer +32 (0)472 79 10 42 of via [email protected].
Uitvoeren van validatiestudies en testen in het kader van routine herkwalificaties en kwalificaties van nieuwe sterilisatiesystemen.
Testen uitvoeren volgens testscripts opgesteld door de betrokken projectingenieur.
Verwerken, evalueren en rapporteren van testresultaten volgens GMP-richtlijnen.
Coördineren of zelf uitvoeren van onderzoeken bij afwijkende of niet-conforme resultaten.
Actualiseren van GMP-documentatie (protocollen, rapporten, procedures) na uitvoering van de studies.
Opleiden en ondersteunen van nieuwe teamleden binnen het validatieteam.
Waken over veiligheid, kwaliteit en naleving tijdens alle validatieactiviteiten.
Profiel
Bachelor in een wetenschappelijke richting (chemie, biotechnologie, farmaceutische technologie, …) of gelijkwaardig door ervaring.
Ervaring binnen een GMP-omgeving en/of met validatieprocessen is een pluspunt.
Perfecte kennis van het Nederlands en een goede kennis van het Engels (schriftelijk en mondeling).
Analytisch en probleemoplossend vermogen met oog voor detail.
Sterke communicatieve vaardigheden en een echte teamspeler.
Technisch inzicht en interesse in technologie (meetapparatuur, software, automatisering, …).
Goede technische schrijfstijl en nauwkeurige manier van werken.
In staat om prioriteiten te stellen en zelfstandig te werken.
Veiligheids- en kwaliteitsbewust.
Bereid om te werken in een tweeploegenstelsel (6u–14u en 14u–22u).
Our offer? Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. You’re interested in this job? We kindly invite you to apply or send me your CV, [email protected]
Construction Manager Brabant Walloon – contracting Our partner is looking for a Construction Manager to join its team. This international company is well-known for its pharmaceuticals. Your responsibilities?
Coordinate construction activities and liaise with the Host Site EHS team
Review safe methods of working ahead of work starting
Lead daily safe work planning sessions e.g. SPA, RAMS, PTW
Participate in daily prestart workforce safety briefings
Participate in safety meetings and lead daily safety walks of the site
Participate in toolbox talks
Assist in incident investigation
Induct / orientate the workers
Identify and control new workers
Identify general and specific safety hazards to the workers
Inspect and conduct safety audits of tasks and safe systems / processes
Ensure that all incidents are reported
Participate in incident investigations
Ensure workers only carry out tasks for which they are trained and qualified
Ensure risk assessments and method statements are in place and in use
Encourage and participate in the behavioral safety system
Intervene and correct any unsafe conditions
Participate in safety meetings
Ensure good housekeeping and organised tidiness (5S) at all times
Your profile?
Experience in construction management of medium and large capital projects
EHS experience
Project and people management skills with thorough knowledge of construction
Communication and collaboration skills
Our offer? Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to training in technical matters and soft skills. We will be your career partner for each step along the way.
Validation Engineer Brabant Walloon – contracting Our partner is looking for a Validation Engineer to join its team. This international company is well-known for its pharmaceuticals. Your responsibilities? The department is, amongst other expertise, in charge of the implementation of health authorities Facility Design requirement for all manufacturing building in the Belgium sites. A new task is required : implementing internal standards of the company (Engineering Standard) You will be responsible for leading the implementation of this new standard in several steps :
Gap analysis between Engineering Standard and Belgium SOP’s
Support and lead risk assessment issuing for each unit with local SMEs
Follow up and track progress on assessment issuing as per milestone.
Participating in the assessment to standardize inter manufacturing units evidences and assessment (same answer for requirement, adding and suggest control or mitigations, identifying gaps).
Possibly, support the Unit to edit remediation plans for gaps identified.
Furthermore, the candidate leads the reporting to Engineering Standard Duty holder and sponsor.
Your profile?
Scientific university degree (Engineer in Chemistry, biochemistry, or Pharmacist,…)
Experience in Product & Process
Experience in project management
Risk assessment
Successful experience in stakeholders management
Excellent organization skills and ability to operate effectively in a multicultural, matrix organization where the workload requires balancing multiple responsibilities simultaneously
Fluent in French et English
Our offer? Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to training in technical matters and soft skills. We will be your career partner for each step along the way. You’re interested in this job? We kindly invite you to apply. Do you have any questions? You can contact Anaïs Malikian, [email protected]
Are you a detail-oriented communicator with a love for strategy and collaboration? And want to make a difference in a fast-paced, purpose-driven industry? Join us as our Tender Specialist and help shape the future of healthcare.
Key Responsibilities: As our Quote and Tender Specialist, you will support the tendering process by preparing tender answers based on the financial, technical and administrative response, internally collected in accordance with the public procurement code. You are a strategic connector, guiding our responses from the first inquiry to final submission. What you will do:
Identifying, reviewing and analyzing tender documents and requirements.
Coordinating bids with cross-functional teams (Sales, Legal, Service, Project Managers, etc.).
Ensuring strong, close and on time collaboration.
Keeping everyone aligned and informed—you’re the go-to hub for info sharing.
Spotting risks early and help ensure compliance and quality check of all documents before submission.
Maintaining organized records of all tenders.
Liaising with customers, suppliers, and partners to gather the right info.
Reporting regularly on tender progress and win strategies.
Your Profile:
You are fluent in Dutch, French, and English (written + spoken).
You have a bachelor’s degree in business, Economics, Law, or related field.
You have experience in tenders, procurement, or sales support, this is essential.
Proficient in use of Microsoft Office tools (Word, Excel, Outlook, Teams, PowerPoint) with speed and accuracy.
You are an excellent multitasker & time manager, who meets tight deadlines with ability to work under pressure.
What we offer:
You will receive an ongoing contract with Manpower Talent Based Outsourcing.
You will get a competitive salary with various additional benefits:
Meal vouchers per worked day;
Group and hospitalization insurance;
Home office expense reimbursement;
Commuting allowance;
Option for flexible working hours and remote work;
32 vacation days
39h workweek
You will receive ongoing support and coaching from your personal consultant at Manpower Talent Based Outsourcing.
You will have the opportunity to attend training sessions to continue your professional growth.
Who are we: At Manpower Talent Based Outsourcing (TBO), we offer outsourcing and contracting opportunities with various international and national companies. As our associate, you will work on a project at one of our clients. These projects range from short-term (at least 3 months) to very long-term (several years). We specialize in the fields of Administration, Healthcare Support, Logistics & Automotive, and Sales & Marketing.
Business Consultant / Account Manager – Talent Based Outsourcing
(Logistiek & Automotive)
Ben jij een commerciële en gedreven professional die het verschil kan maken voor klanten én consultants? Wil je werken in een dynamische omgeving waar initiatief en flexibiliteit gewaardeerd worden? Dan is deze functie bij ManpowerGroup – Talent Based Outsourcing iets voor jou!
Wat ga je doen?
Als Business Consultant / Account Manager ben je een belangrijke schakel in ons kleine, maar hechte team. Je takenpakket omvat:
Actief klantenbeheer: onderhouden en uitbouwen van relaties met logistieke en automotive klanten.
Projectopvolging van consultants: begeleiden van consultants en freelancers via 1:1 gesprekken, evaluaties en praktische ondersteuning op projecten.
Prospectie & acquisitie: identificeren van nieuwe businesskansen en werven van zowel klanten als geschikte kandidaten.
Werving & selectie: zoeken, aantrekken en matchen van talent voor projecten bij klanten.
Contract- en projectmanagement: bewaken van contracten, budgetten en projectresultaten, in samenwerking met interne teams.
Wie ben jij?
Je hebt een commerciële en resultaatgerichte mindset.
Je voelt je comfortabel in gesprekken met klanten én consultants.
Je hebt ervaring met accountmanagement, projectmatig werken en/of werving & selectie.
Je bent flexibel en ondernemend, en vindt het leuk om initiatief te nemen binnen een klein team.
Kennis van de logistieke of automotive sector is een pluspunt, maar geen vereiste.
Wat bieden wij?
Contract onbepaalde duur met ManpowerGroup Solutions (Talent Based Outsourcing)
Your responsibilities: Commissioning and Qualification: Review IQOQ protocols and reports to ensure the qualification of CPP, support the team for risk analysis creation (SRA), review equivalence certificate, write validation plans…
Validation: According to the client’s standards and procedures, design the validation strategy through PQ protocol redaction, ensure the readiness for PQ validation, coordinate validation (on the floor job expected), manage unplanned events associated with validation, be the contact with QC.
Product validation: Understand the product validation lifecycle and ensure that the validation strategy is in line with the product validation strategy, support the product steward in product related topic (E&L, holding time, …).
Change Control: Assessment of the validation impact through eCC assessment (Stakeholder role expected), Coordinate eCC, and be responsible of eCC tasks.
Project management: Plan and manage PQ activities (material, documentation, people…), support the project planner, animation of meetings/workshops, help the production representative in the understanding of validation requirements.
Your profile:
University degree (Biotechnology, Agronomy, Chemistry or Pharmacy).
At least 5 years’ professional experience in pharmaceutical environment, in quality and validation environment.
Good oral and written communication skills in French & English (for efficient communication with engineering office and suppliers).
Good Knowledge of GMP Regulated environment related to validation activities.
Good interpersonal relationship skills – To be a good team player to success in each validation.
Problem solving and achievement oriented.
Be organized.
Nice to have:
Knowledge of freezer dryers, filling lines and isolators would be an asset.
To maintain and keep up to date its knowledge and experience necessary to the function.
Ability to take decisions in stressful conditions.
Proactive and ready to take the lead to make things happen.
Ability to work under pressure on multiple deliverables within project timelines.
Our offer? Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. Are you interested in this job? I kindly invite you to apply or send me your CV, [email protected]
Your responsibilities: The Manufacturing Science, Analytical and Technology department (MSAT) represents the scientific backbone of the company that provides commercial manufacturing support, process/method optimization (lifecycle management), technology transfer of new products and processes/methods and innovative, robust, and cost-effective next-generation processes/methods. To accommodate these complex scientific roles, the MSAT has extensive state-of-the-art laboratory capacity on site to develop and implement lab-scale models and analytical methods.
The company has engaged in a company-wide digitalization program that aims to integrate all (non-GMP) MSAT laboratory-related activities into iLab, a software package that is completely transforming the daily lab activities from paper-based to digital (including raw material inventory, notebooks, task management, data management) and allow for data collection and analysis on a global scale. This digital transformation entails the development of electronic notebook methods and the connectivity of laboratory equipment to ensure an efficient way of working.
Your profile:
You are familiar with laboratory informatics e.g. laboratory and data management systems and digital lab solutions
You have a PhD or master in Life Sciences, with relevant experience of minimum 3 years in biotech process/analytical development or MSAT-like functions.
Since all writing is in English and given the international context, you are fluent in writing and talking in English.
You are used to work in a lab environment and have specific experience in growing mammalian cells in bioreactors and/or protein purification and/or analytical assays.
You are flexible to adapt to changing priorities and willing to learn at a rapid pace.
You have affinity with IT systems and have an exploratory mindset to search for digital solutions in a laboratory environment.
You are a strong and spontaneous communicator who is eager to resonate with people across an organization, discuss and find compromises with people from different MSAT sub-teams.
You have an excellent analytical and problem-solving mindset, are accurate with the necessary eye for detail.
Our offer ? Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. You’re interested in this job? We kindly invite you to apply or send me your CV, [email protected]
Product Quality as the independent quality authority for product-related qualifications and validations of the assigned products.
Compliant and right first-time product launches within Quality Operations (QO)
Regulatory CMC (= Chemistry, Manufacturing & Controls) compliance of the plant processes with the regulatory filings
Validation Act as quality authority in a consistent way, in compliance with cGMPs and current regulatory expectations, for the following qualification and validation documents:
Process qualification/validation
Method validation
Filter validation
Component qualification
Raw material evaluation
DHF
Registration The composition, production processes, specifications, analytical methods of the drug products are described in the registration dossiers of the different markets. The QPA is responsible for pursuing regulatory CMC compliance of the site practice versus the registration dossiers. This is achieved by participating in the following processes:
Data verification and QA review of initial marketing authorization filings and variations, responses to health authority queries, briefing documents for scientific advice meetings;
Performing compliance checks of the registration dossiers of the different markets versus the site practice.
Implementation Ensure correct and timely implementation of approved regulatory changes in the site: follow-up on approvals and commitments in the different markets.
Your profile:
Master’s degree in scientific discipline
2 years of relevant experience in the pharmaceutical sector and/or medical device industry with specific experience or interest in Quality Assurance or Compliance and in regulatory affairs (CMC) for pharmaceutical products.
Quality mindset
Pragmatic
Excellent analytical and problem-solving skills
Excellent oral and written communication skills and social skills
Scientific knowledge and skills
Languages: fluent in Dutch and English
Excellent knowledge of cGMP, regulatory guidances and relevant medical device and combination product regulations.
Our offer: Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. Are you interested in this job? We kindly invite you to apply or send me your CV, [email protected]
Heb jij een passie voor techniek en leiderschap en wil je een tastbare impact maken op het eindresultaat van prefab-projecten? Dan is deze job iets voor jou!
Voor onze klant regio Aalter zijn we op zoek naar een Atelierverantwoordelijke. Zin om deze uitdaging aan te gaan via Jefferson Wells? Lees dan alvast onderstaande functie-inhoud!
Jouw verantwoordelijkheden? Als Atelierverantwoordelijke Prefab combineer je jouw technische expertise met leidinggevende capaciteiten, begeleid je jonge collega’s en optimaliseer je processen in het atelier. Jouw takenpakket:
Lezen, controleren en meten van isometrieën.
Beheersen van verschillende lasprocessen en materiaalsoorten.
Opstellen van het plan van aanpak in de prefab, inclusief selectie van spoolstukken, lasproces en lasplan, in overleg met het team.
Meewerken tijdens de opstartfase of drukke momenten in het atelier.
Toezicht houden op veiligheid, kwaliteit van het laswerk, maatvoering en haaksheid.
Bewaken van correct gebruik van machines (zaagmachine, pendelaar, kolomboor, …) en stimuleren van zorgzaam gebruik.
Monitoren rendement van de prefabactiviteiten in samenspraak Project Manager.
Invullen van alle noodzakelijke documenten ter ondersteuning van het prefabproces
Wie ben je? Je beschikt over een technisch diploma en hebt ruime technische kennis op het vlak van lassen, montage en prefab. Je bent een geboren leider en coach, bij voorkeur met ervaring in een technische of industriële omgeving. Je kan werkzaamheden efficiënt plannen, coördineren en monitoren, met oog voor kwaliteit en veiligheid. Daarnaast deel je graag je kennis met jonge collega’s en geef je constructieve feedback.
Wat kan je verwachten? Je komt terecht in een dynamische en innovatieve organisatie waar teamwork, vakmanschap en persoonlijke ontwikkeling centraal staan. De rol biedt een aantrekkelijk loonpakket, inclusief extralegale voordelen en de mogelijkheid tot een bedrijfswagen.
Voldoet deze functie aan jouw verwachtingen of wil je meer informatie? Solliciteer dan rechtstreeks via deze website of contacteer Sara Van den Bossche op het nummer +32 (0)472 79 10 42 of via mail [email protected].
