QC NCE Technician Senior Contracting – Brabant Wallon Your Responsibilities:
Plan and conduct laboratory work, focusing on preparing documentation and analyzing experimental results.
Spend most of your time in the laboratory conducting experiments, while ensuring accurate and detailed documentation.
Focus on the administrative aspects of analyses, including report writing and reviewing protocol reports.
Take immediate action when problems arise, ensuring a smooth workflow and maintaining high productivity.
Collaborate closely with the team, sharing insights and consulting on methods as needed.
Your Profile:
Experience: A minimum of 4-5 years of experience, with expertise in the administrative aspects of analyses, such as report writing and protocol review.
Pharma Experience: Experience in the pharmaceutical industry is essential.
Team Spirit: Ability to work effectively within a collaborative and dynamic team environment.
Critical Thinking: Strong analytical skills, with the ability to make informed decisions based on existing knowledge and analyses.
Language Skills: Good understanding of both French and English. You should be able to write and comprehend methods in English, with the ability to work in English essential.
Energetic & Positive: A proactive, positive attitude is crucial to thrive in a fast-paced, team-oriented environment.
Knowledge of analytical techniques such as RM (Risk Management) is a plus.
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] QC NCE Technician Senior Contracting – Brabant Wallon Your Responsibilities:
Plan and conduct laboratory work, focusing on preparing documentation and analyzing experimental results.
Spend most of your time in the laboratory conducting experiments, while ensuring accurate and detailed documentation.
Focus on the administrative aspects of analyses, including report writing and reviewing protocol reports.
Take immediate action when problems arise, ensuring a smooth workflow and maintaining high productivity.
Collaborate closely with the team, sharing insights and consulting on methods as needed.
Your Profile:
Experience: A minimum of 4-5 years of experience, with expertise in the administrative aspects of analyses, such as report writing and protocol review.
Pharma Experience: Experience in the pharmaceutical industry is essential.
Team Spirit: Ability to work effectively within a collaborative and dynamic team environment.
Critical Thinking: Strong analytical skills, with the ability to make informed decisions based on existing knowledge and analyses.
Language Skills: Good understanding of both French and English. You should be able to write and comprehend methods in English, with the ability to work in English essential.
Energetic & Positive: A proactive, positive attitude is crucial to thrive in a fast-paced, team-oriented environment.
Nice to Have: Knowledge of analytical techniques such as RM (Risk Management) is a plus.
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]
Validation Engineer – Computerized Systems Vast Contract of Freelance – Regio Wommelgem #Validatie #GAMP5 #Automatisering
Beschik jij over een hoger technisch diploma, heb je ervaring met geautomatiseerde controlesystemen en een passie voor validatie binnen een GMP-omgeving? Op zoek naar een uitdagend project waar je deze expertise kan inzetten? Dan is deze job zeker iets voor jou!
Voor een grote, internationale speler in de farmaceutische industrie zijn we op zoek naar een enthousiaste Validation Engineer – Computerized Systems. Voel jij je klaar voor deze uitdaging? Wil je samen met Jefferson Wells deze opdracht aangaan? Lees dan zeker verder!
Jouw verantwoordelijkheden? Als Validation Engineer maak je deel uit van een multidisciplinair projectteam. Je zal verantwoordelijk zijn voor:
Schrijven van commissioning- en kwalificatietesten op basis van gebruikersvereisten en functionele specificaties
Uitvoeren van validatietesten op een nauwkeurige en GMP-conforme manier
Uitvoeren van risicoanalyses
Fungeren als aanspreekpunt voor alle validatiegerelateerde vragen, zowel intern als extern
Opvolgen van projectplanningen en milestones
Wie ben je? Om de rol van Validation Engineer succesvol in te vullen, beschik je over een Bachelor- of hogere technische opleiding en heb je minstens twee jaar relevante ervaring idealiter binnen een GMP-omgeving in de farmaceutische sector. Daarnaast heb je affiniteit met geautomatiseerde systemen zoals PLC's en SCADA. Je combineert een sterke analytische ingesteldheid met uitstekende communicatieve vaardigheden en weet vlot te schakelen tussen het Nederlands en het Engels. Een praktische kennis van Office-toepassingen zoals Word, Excel en Outlook is essentieel. Tot slot ben je bereid om sporadisch te reizen voor je werk.
Wat kan je verwachten? Als Validation Engineer krijg je een aantrekkelijke verloning aangevuld met een uitgebreid pakket extralegale voordelen en een onmiddellijk vast contract van onbepaalde duur. Daarnaast geniet je de mogelijkheid om jezelf zowel persoonlijk als professioneel verder te ontwikkelen door interne trainingen en opleidingen. Ook freelancers kunnen in aanmerking komen.
Voldoet deze vacature aan jouw verwachtingen? Aarzel dan niet om te solliciteren via de website of contacteer Sara Van den Bossche op het nummer (+32) 472 79 10 42 of stuur je CV naar [email protected].
QC NCE Technician Contracting – Brabant Wallon Your Responsibilities
Plan and conduct laboratory experiments.
Prepare and maintain detailed documentation of experimental results.
Spend the majority of the time working in the laboratory.
Ensure high productivity and efficiency in completing tasks.
Act promptly and effectively when problems arise.
Collaborate with team members to discuss methods and results.
Your Profil :
Experience: A minimum of 2-3 years in a similar role is required.
Pharma Experience: Previous experience in the pharmaceutical industry is essential.
Team Spirit: Strong ability to work collaboratively in a dynamic team environment.
Critical Thinking: Ability to analyze data and make informed decisions.
Language Skills: Good understanding of both French and English. Proficiency in English is essential for reading and understanding methods.
Energetic & Positive: You should bring a proactive, positive attitude to the team.
Knowledge of analytical techniques such as RM (Risk Management) is a plus.
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]
Adaptation Engineer Vast Contract of Freelance – regio Gent #Engineering #Production #Technicaladaptation
Ben je geboeid door de wereld van Production Engineering? Vindt je uitdaging in het uitwerken van technische aanpassingen binnen klant specifieke en innovatieve projecten? Dan hebben we een geweldige opdracht die perfect bij jou past!
Voor een klant zijn we op zoek naar een Adaptation Engineer regio Gent (m/v/x). Voel jij je klaar voor deze uitdaging? Wil je samen met Jefferson Wells aan de slag bij deze klant? Lees dan verder!
Jouw verantwoordelijkheden? Als Adaptation Engineer werk je nauw samen met de project engineers en de process engineers. Je takenpakket:
Je werkt technische oplossingen uit en documenteert niet-standaard concepten.
Je ontwerpt in Autcad en geeft advies over technische aanpassingen voor klant specifieke ontwerpen.
Je neemt zelfstandig beslissingen met eindverantwoordelijkheid over de concepten.
Wie ben je? Om bovenstaande taken succesvol uit te voeren, beschik je als Adaptation Engineer over een technische bachelor- of masteropleiding of gelijkwaardig door ervaring. Ervaring is geen must, maar interesse in automotive onderdelen en productie des te meer. Je bent communicatief en houdt ervan om in teamverband te werken. Daarnaast ben je organisatorisch en administratief onderlegd. Je gaat zelfstandig te werk en bent nauwkeurig ingesteld. Jouw kennis van MS Office is uitgebreid en je beheerst de Engelse en Nederlandse taal volledig. Andere talen zijn een voordeel.
Net afgestudeerden zijn ook welkom voor deze job!
Wat kan je verwachten? Als Adaptation Engineer kom je terecht in een dynamische en open werkomgeving met aangename collega’s. Bovendien krijg je een mooie verloning aangevuld met een uitgebreid pakket aan extralegale voordelen en een onmiddellijk vast contract van onbepaalde duur. Ten slotte geniet je de mogelijkheid om jezelf persoonlijk en professioneel te ontwikkelen door interne trainingen en opleidingen.
Voldoet deze functie aan jouw verwachtingen? Solliciteer dan rechtstreeks via de website of contacteer Sara Van den Bossche op het nummer +32 (0)4 72 79 10 42 of via Sara.vandenbossche(@)jeffersonwells.be.
Process Engineer Vast Contract of Freelance – regio Gent #Engineering #Productie #Procesoptimalisatie
Ben je geboeid door de wereld van productie en innovatie? Heb je een sterke interesse in procesoptimalisatie en ben je gepassioneerd door op maat producties binnen een uitdagende productieomgeving? Dan hebben we een geweldige opdracht die perfect bij jou past!
Voor een klant zijn we op zoek naar een Process Engineer regio Gent (m/v/x). Voel jij je klaar voor deze uitdaging? Wil je samen met Jefferson Wells aan de slag bij deze klant? Lees dan verder!
Jouw verantwoordelijkheden? Als Process Engineer ben je verantwoordelijk voor het beheren en optimaliseren van de niet-standaard specificaties binnen de productieomgeving.
Je bent verantwoordelijk voor het verwerken van de ‘niet-standaard concepten’ in onze interne systemen.
Je maakt diverse montage-instructies en zorgt voor de nodige updates.
Je verzamelt informatie rond het productieproces en zorgt ervoor dat de monteurs de nodige instructies ontvangen.
Je volgt complexe of kritische klantspecifieke orders op de lijn op.
Je bent het aanspreekpunt voor alle problemen omtrent deze specificatielijsten en dit voor diverse stakeholders.
Je zorgt ervoor dat onze logistieke afdeling de juiste informatie omtrent wijzigingen in het logistieke proces ontvangt.
Wie ben je? Om bovenstaande taken succesvol uit te voeren, beschik je als Process Engineer over Master of Bachelor diploma in een technische opleiding. Je hebt een goede kennis van assemblageprocessen; kennis van productiesystemen is een pluspunt. Je kunt zelfstandig werken en hanteert een proactieve aanpak. Daarnaast ben je nauwkeurig en detailgericht in administratieve taken en heb je een goede kennis van MS Office (Word, Excel en PowerPoint). Je hebt een sterk probleemoplossend vermogen en een sterk analytisch vermogen. Je bent een echte teamplayer en houdt van cross-functioneel werk
Wat kan je verwachten? Als Process Engineer Niet-Standaard Productie kom je terecht in een dynamische en open werkomgeving met aangename collega’s. Bovendien krijg je een mooie verloning aangevuld met een uitgebreid pakket aan extralegale voordelen en een onmiddellijk vast contract van onbepaalde duur. Ten slotte geniet je de mogelijkheid om jezelf persoonlijk en professioneel te ontwikkelen door interne trainingen en opleidingen.
Voldoet deze functie aan jouw verwachtingen? Solliciteer dan rechtstreeks via de website of contacteer Sara Van den Bossche op het nummer +32 (0)4 72 79 10 42 of via Sara.vandenbossche(@)jeffersonwells.be.
Secondary Packaging Industrialization Expert Contracting – Brabant Wallon Your Responsibilities
Lead packaging projects from initial design through to industrialization and lifecycle management of secondary and tertiary packaging solutions.
Provide technical expertise to internal sites, affiliates, and CMOs to ensure process efficiency, quality, cost optimization, and alignment with environmental objectives.
Manage projects, including change control processes, team communication, stakeholder engagement, and reporting to management.
Ensure compliance with international standards, regulations, and internal guidelines related to secondary and tertiary packaging.
Act as a subject matter expert for troubleshooting and optimization of packaging components and processes.
Support cross-functional teams, including purchasing, marketing, and supply chain, on technical packaging matters.
Lead and coordinate tech transfers, validation, investigations, and business support for packaging-related activities at internal and external sites.
Supervise communication and collaboration with one or more packaging sites.
Contribute to team objectives, planning, documentation, and continuous process improvements.
Your Profile · Proven experience in secondary/tertiary packaging within a pharmaceutical GMP manufacturing environment. · Hands-on experience in pharmaceutical project management, including tech transfers, product launches, and adapting to new regulations. · Strong analytical and conceptual thinking skills with the ability to understand complex technical and business challenges. · Capable of managing multiple projects and priorities efficiently, from development through commercialization. · Autonomous and pragmatic, with a proactive, problem-solving mindset and the ability to drive initiatives forward independently. · Demonstrated ability to work effectively within cross-functional and multidisciplinary teams. · Fluent in English (written and spoken); French is a plus. · Excellent communication skills, both written and verbal. · Positive and collaborative attitude with a strong sense of ownership. · Experience with artwork management is an advantage.
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]
Biomanufacturing Support USP Contracting – Brabant Wallon Your Responsibilities · Perform routine documentation and development-related tasks, while also addressing urgent technical issues (e.g., equipment or process failures). · Conduct technical investigations and ensure proper documentation of findings and actions. · Actively contribute to both planned and emergency tasks, showing flexibility and responsiveness. · Work closely with system teams, labs, and external subject matter experts (SMEs) to ensure seamless service integration. · Play a central role in coordinating development efforts and cross-functional collaboration. · Support ongoing projects and be fully involved in daily operations, ensuring a strong understanding of field and lab processes. · Demonstrate a high level of on-site engagement, especially during the first weeks, to ensure full integration and commitment.
Your Profile · Proven ability to manage complex expectations and contribute to project success in dynamic environments. · Strong background as a development writer, ideally in geo-related or technical development projects. · Autonomous and adaptable, with the ability to work independently in fast-paced and high-compliance settings. · Experience with service integration and cross-team coordination is essential. · Solid understanding of pharmaceutical processes and standards is important. · Excellent interpersonal and communication skills, with a proactive, field-oriented mindset. · Must enjoy being hands-on and present on-site, engaging directly with operational teams. · Fluent in English (written and spoken)
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]
Be the central QA point of contact for the organization for investigations/deviations/ out-of-specifications/ audit observations associated with the assigned vendors. Perform the QA review of deviation notifications, retrieve and collect supportive information from involved stakeholders (Vendor Team, GQL, CAS, Business) to allow assessment.
Manage the key performance indicators (metrics) for key operational QA activities and services associated with the vendors in the defined described tracking tools (Vendor QA KPI tracker, SpiderImpact) and track the vendor’s performance
Ensure all Quality agreements are in place and take ownership of agreements for the vendors. Maintain Quality Agreement with the vendors up to date and perform periodic reviews and update of the agreement in close collaboration with the product GQLs and the vendors.
When applicable, be sure that the Annual Product Stability Program is rolled-out and executed at the vendor in accordance with the Stability Program
Ensure the Product Quality Reviews (PQR) are completed by the vendors in a timely manner and as needed, are reviewed within the requested time period. Ensure that this review is documented and made available in the Controlled Documents System.
Participate as QA representative to the recurrent vendor meetings, present issues and resolutions, and drive vendor quality performance through these meetings
Quality Complaints: Be the contact person for the follow-up with vendors for the manufacturing investigation part. When applicable, ensure that initial receipt, logging of quality complaints into the Complaint System and provision of responses to the complainant are professionally coordinated and managed.
If needed work with the Vendor team and Global Quality Lead to determine the Root cause of issues which may lead to a Corporate Technical Review (CTR) meeting. Coordinate vendor quality related investigations
Participate on ad-hoc basis to the Product Change Control Committees for activities related to the vendors
Provide expert QA advice, support and management for technical operational QA and general QA matters associated with the vendors
Work closely with Corporate QA teams, Technical Operation Teams, Business stakeholders and Affiliates in an effective and efficient way
Cover the entire product life cycle from initial commercialization including Technology Transfer/Knowledge transfer, commercial (key raw materials to distribution), product improvements to phase out for the assigned vendors
Developer and owner of the QA plans and product resource and capacity overview for activities associated with the assigned vendors
Ensure all relevant documentation are provided to the vendors and implemented (Methods, Specs, Master Batch record)
Ensure review of relevant RA dossier section related to the assigned vendors
Have the overview of audit and HA inspections related to the vendors. Track and follow-up on Audit observation and CAPA plan implementation at the vendor.
Be the QA stakeholder for Vendor Risk management.
Manage and control quality documents related to the vendors in the Controlled Documents System
Support on customer audits and Health Authority inspections at the vendors, as needed
Receipt, coordinate review and authorize product reworks and repackaging
Be the point of contact for post-release vendor issues (supply chain, distribution, etc.)
As required provide Operational QA support to other vendors
Act as substitute for other Vendor Quality Leads in times of absenteeism (e.g. vacation, illness)
Act as a coach for VQL’s with less experience.
Work in accordance with HSE and Corporate policy requirements and drive personal training and development activities to meet the needs of the business and professional career development.
Act as Best Practice ambassador, leads best practices steams and uses knowledge of internal/external business environment to improve existing process
Your profile:
Master’s degree in Sciences
Must be knowledgeable in several areas of the global pharmaceutical industry, including the interpretation and practical application of applicable regulations. Has good background knowledge of the pharmaceutical industry from a business and technical perspective.
Must be able to work independently and handle complex / difficult situations. Output from actions will most likely impact activities across several departments.
Possess good auditing capabilities and skills.
Must be able to effectively interact with and influence senior internal and external personnel on many aspects of project and product related matters.
Must have the ability to manage projects / activities across global geographies within the area of expertise. Be capable of leading and motivating teams and demonstrate professional maturity in difficult situations. Set challenging objectives for self and others and drive for results.
Root cause and risk management/assessment skills
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]
Document and Records Management Expert Contracting – Brabant Wallon Your Responsibilities
Perform quality control on non-clinical documents (protocols, amendments, reports, etc.).
Ensure compliance and readiness of documents for regulatory submissions.
Upload, index, and track documents in the Veeva Vault EDMS.
Oversee the document lifecycle, ensuring adherence to quality standards and GLP requirements.
Liaise with stakeholders (authors, QA, RA, etc.) to follow up on corrections and approvals.
Provide training and guidance to internal users on good documentation practices.
Participate in process reviews and continuous improvement initiatives for documentation workflows.
Your Profile
Minimum 8 years of experience in the pharmaceutical industry.
Strong background in regulated documentation management (GLP, GCP, etc.).
Deep understanding of non-clinical documentation and its lifecycle.
Hands-on experience with Electronic Document Management Systems (EDMS), preferably Veeva Vault.
Familiarity with regulatory requirements for submission-ready documents.
High level of digital literacy.
Comfortable working in high-compliance, traceability-focused environments.
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]
Vous avez de l'expérience dans la gestion de fournisseurs, l'amélioration des performances logistiques et la conduite d'audits de capacité ? Vous êtes à l’aise dans un rôle de coordination, d’analyse et de coaching ? Cette opportunité est pour vous !
Notre partenaire, un leader international dans le secteur de l’industrie / transport, recherche un Supplier Delivery Performance Manager pour renforcer son équipe basée à Bruges. L’entreprise est reconnue pour ses innovations technologiques, sa culture de formation continue et son engagement durable.
Vos responsabilités ?
En tant que Supplier Delivery Performance Manager (SDPM), vous êtes responsable de la fiabilité des livraisons fournisseurs et vous jouez un rôle clé dans la prévention et la gestion des risques logistiques.
Vos tâches principales incluent :
Évaluer la capacité de production et la maturité supply chain des fournisseurs via des audits ciblés.
Analyser les causes racines des non-performances et mettre en place des plans d'action.
Gérer les crises de livraison (mono-site ou multi-site).
Piloter des plans d’amélioration pour les fournisseurs sous-performants.
Accompagner et former les Material Planners aux méthodes SDPM.
Participer au développement de la roadmap APSYS et à la standardisation des processus.
Travailler en collaboration avec les parties prenantes lors de problématiques majeures.
Respecter et promouvoir les politiques EHS et les règles d’éthique Alstom.
Votre profil ?
Vous êtes titulaire d’un diplôme universitaire (Master ou Bachelier) en logistique, ingénierie, économie ou domaine équivalent et justifiez d’une expérience dans un environnement industriel ou supply chain.
En plus de cela :
Vous avez une bonne expérience en gestion des fournisseurs et gestion des risques.
Vous êtes analytique, orienté solution et bon communicateur.
Vous parlez couramment le français et l’anglais ; le néerlandais est un plus.
Vous travaillez de façon autonome et êtes résistant au stress.
Ce que nous vous offrons ?
Un contrat à durée indéterminée dans un environnement dynamique et international avec :
Horaire flexible et possibilité de télétravail
Assurance groupe et hospitalisation
Plan cafétéria (leasing voiture/vélo, électronique, coaching, …)
Opportunités de développement personnel via des formations internes
Vous vous reconnaissez dans ce profil ? Postulez directement via notre site web ou contactez Jan au +32 (0)494 16 31 09 ou via jan.vangrembergen@jeffersonwells.be
