61 Vacatures voor Qa Manager in de Nederland
Quality Control Employee
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We are looking for an energetic person for the position of Quality Control Employee, who ensures that our blueberries and asparagus always arrive on time and in perfect condition to the clients!
In this role, you will:
- Check and register incoming and outgoing batches of berries in the system
- Perform quality checks during the packaging process
- Test the shelf life of products
- Monitor the hygiene of the production lines, staff, and production environment
Actively contribute ideas for quality improvements
Working hours:
- Morning shift: 06:00 – 14:00
- Afternoon shift: 11:45 – 20:00
- Peak season: 13:45 until as late as 22:00–23:00
Do you enjoy dynamic work, have an eye for detail, and are you not afraid to stay active? Then join us! Every day with us is about delivering the best quality and… good work!
Over het bedrijfOur client is a dynamic and growing family business, specializing in cultivating, sorting, and packaging blueberries and asparagus. What makes them strong? The combination of their own cultivation and close cooperation with growers from Europe, Africa, and South America. With modern facilities in Horst and advanced technology, they deliver fruits and vegetables that meet the highest quality standards. Our client manages every stage – from the field to the final packaging. Because for them, it’s all about taste, freshness, and customer satisfaction.
Wat wij vragen- MBO level of working and thinking, preferably in nutrition, fresh produce (AGF), or quality
- Affinity with fresh products and quality control
- Proficiency in Dutch and English, both spoken and written; knowledge of Polish is a plus
- Strong communication and social skills
- Flexible attitude, both in work approach and working hours
- Positive, energetic, and proactive work mentality
- You contribute to an efficient and high-quality packaging process and collaborate with your colleagues to achieve the best results every day
These skills are essential to start working as a Quality Control Employee in Horst. But what also matters to us is who you are. We would love to learn about your talents, experience, and ideas.
Wat wij bieden- Hourly wage between €16.95 and €9.66, depending on knowledge and experience
- 25% shift allowance for evening shifts (19:00 – 23:00)
- Travel allowance of €0 per km (from 10 km, up to a maximum of 30 km one way)
- Annual salary increase from January 1st – we value your development
- Working in a cold storage room (10°C) – we provide warm and comfortable work clothing
A stable job at an innovative company with prospects for long-term employment
Are you ready to take on this vacancy as a Quality Control Employee in Horst? You can apply in just 2 minutes.
Have questions first? We’re here to help: / or email: / . Good work!
Quality & Control Stage
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We offer you an Ocean of Possibilities. Join our family.
About Us
Damen Shiprepair Amsterdam is onderdeel van de Damen Shiprepair en Conversion Group. De organisatie kenmerkt zich door een moderne bedrijfsvoering waarbij de klant centraal staat en efficiënt kan worden ingespeeld op de marktomstandigheden. Op de werf zijn alle faciliteiten aanwezig om onze klanten een full service pakket te bieden. Damen Shiprepair Amsterdam repareert uiteenlopende typen schepen tot een lengte van 250 meter. Wij werken met 110 medewerkers in vaste dienst en, afhankelijk van het werkaanbod, een flexibele schil van inleenpersoneel.
De werf in Amsterdam Noord kenmerkt zich door een sterk- en gedreven team die allen dezelfde passie delen voor de scheepsreparatie. Hier wordt hard gewerkt, maar ook hard gelachen. Op de werf hebben wij een personeelsbestand bestaande uit wel 25 verschillende nationaliteiten. Daarnaast hebben we constant andere schepen op de werf. Dit brengt telkens verschillende soorten projecten, werkzaamheden en klanten met zich mee en zorgt voor een dynamische werkplek waar geen dag hetzelfde is.
Wij zijn een project gedreven organisatie, elk schip dat binnenkomt zien wij als uniek project. We zorgen er samen met elkaar voor dat het schip weer zo snel mogelijk kan varen. Om dit mede mogelijk te maken werken we op basis van klantwensen en eisen, scheepsbouw-normen en wet- en regelgeving.
The role
Tijdens deze periode ondersteun je de werkvoorbereiding met focus op Quality & Control. Je stagebegeleider(s) zullen jou gedurende de stage periode wegwijs maken en leer je meer over de normen en eisen, wet en regelgeving op scheepsbouw gebied.
Key Accountabilities
Je gaat je onder andere bezig houden met het begeleiden van de productie door middel van het Inspection Test Plan (ITP) en Certificaten beheer (ISO-normen) van materialen, toevoegmaterialen, lassers en wps'n. Ook zal je kennis opdoen over de materialen en toevoegmaterialen. Een fitup- las- plan en lasonderzoek plan leer je opstellen en uitwerken tijdens je stage. Wil jij nog veel meer leren en je zelf uitdagen? Dan zien we jouw reactie graag tegemoet
Skills & Experience
- Je beschikt over mbo of hbo werk-denk niveau;
- Je bezig bent met een van de genoemde opleiding: Werktuigbouwkunde, Engineering of Constructietechniek of maritieme opleiding;
- Je houdt van afwisseling en nieuwe uitdagingen;
- Je beschikt over goede communicatieve vaardigheden in het Nederlands en/of Engels.
What We Offer
We willen ervoor zorgen dat je een happy HSEQ Stagiair bent, dus bieden we jou de mogelijkheid om jezelf te ontwikkelen in deze functie.
Ondernemen zit in ons DNA en daarom blijven we groeien, innoveren en volop kansen bieden. Op de afdeling HSEQ kom je samen te werken met de HSEQ manager en nog drie HSEQ collega's.
Wij Bieden Jou
- Persoonlijke begeleiding, vrijheid, afwisselend werk en een werkomgeving waar jouw mening telt.
- Een internationale werkomgeving;
- Open, informele, no-nonsense cultuur met korte communicatielijnen;
- Een goede dosis humor en samenhorigheid (we gaan voor elkaar door het vuur);
- Stage vergoeding van 500 euro bruto per maand met uitzicht op een traineeship of vast dienstverband.
Recruiter
Jessica van Honk
Email
Please apply through the Apply Button. Due to GDPR reasons we cannot accept applications by email.
Quality Control Analyst
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Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds….
ClinChoice is searching for a Quality Control Analyst to join one of our partner companies, a large pharmaceutical company leader in the field of biomedicines. This role is 1 full FTE, hybrid (3 days onsite and 2 days from home) in Leiden, NL, contract through June –8 years of experience in Quality Assurance within the pharmaceutical industry, with strong proficiency in nonconformances (NCs), CAPA, and change control processes.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client counterparts.
Scope of the role:
This role supports quality operations by executing routine and non-routine tasks, leading quality record activities, and coordinating team efforts. The employee helps meet company goals through their performance, communicates effectively, and ensures issues are escalated when needed.
Main Job Tasks and Responsibilities:
- Applies expertise knowledge of Quality requirements to support the execution of Operations unit objectives.
- Perform nonconformance investigations, including CAPA records, and lead change controls (CC) for the Operations unit from initiation through completion.
- Reviews documentation associated with processes and activities for the Operations unit products.
- Maintains procedures and applicable documentation and makes updates based on new or revised regulatory requirements, internal investigations, and audits.
- Ensure compliant documentation and timely completion of quality records.
- Initiates and implements risk mitigations and continuous quality improvement projects, under limited guidance.
- Supports with formal escalation processes to ensure visibility of risks associated with safety, product quality, and regulatory compliance.
- Perform regular GEMBA walks to observe and document adherence to GMP standards on the production floor, identify areas for improvement, and collaborate with team members to implement corrective actions.
- Takes ownership of personal training and ensures that all required training is understood and completed on time.
- Enhance a culture of belonging through trusting, diverse, and inclusive relationships.
Additional tasks and job duties of the position that are not required daily:
- Supports the Subject Matter Expert on non-conformances and Change Controls during inspections and audits.
- Supports developing training programs for general cGMP processes.
- Formulates responses to observations from audits and inspections.
- Conducts data analysis on recurring non-conformances and recommends corrective actions.
Education and Experience:
- A relevant Master's Biological degree with 5-8 years of quality assurance / control experience.
- English B2 language level is required.
- Intermediate proficiency in MS Office.
- Routine proficiency in data analysis.
- Specialist-level proficiency in business applications.
- Positive attitude, proactive, decisive, and organized, with the ability to work independently and in a team.
- Stress-resistant and able to remain calm under pressure.
- High degree of accuracy and a strong quality mindset.
- Flexible and able to adapt to changing priorities.
- Demonstrates accountability by proactively addressing issues and taking responsibility for outcomes.
- Strong analytical thinking skills, including the ability to handle complexity, ask questions, use data and information effectively, identify gaps and root causes, and develop creative solutions.
- Effectively prioritizes tasks to meet deadlines and ensure timely delivery.
- Maintains alignment with stakeholders and builds meaningful connections with customers.
- Previous experience in leading or providing significant guidance on change controls or quality investigations.
- Open to giving and receiving transparent, constructive feedback; learns from mistakes and supports both organizational and personal growth.
- Coordinates team initiatives by providing clear direction and fostering effective collaboration.
The Application Process
- Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for?
About ClinChoice
- ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos
- Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset, and they are the fulcrum around which all ClinChoice activities are built, and close management and training is the core instrument to develop and maintain highly qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.
- ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
- Key words: Quality Assurance (QA), Quality Control (QC), Nonconformance (NC), CAPA (Corrective and Preventive Actions), Change Control (CC), GMP (Good Manufacturing Practices), Quality Records, Risk Mitigation, Continuous Improvement, Regulatory Compliance, Audit Support, Inspection Readiness, Documentation Review, Process Improvement, Deviation Management, Root Cause Analysis, Data Analysis, Training Development (GMP Processes), Quality Control Analyst
Quality Control Medwerker
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Gourmet Ingredients is een jonge organisatie die onderdeel is van Gourmet BV. De wortels van ons bedrijf liggen in de aarde. Hierdoor begrijpen wij de wereld van sjalotten, uien en knoflook als geen ander. Deze kennis van de keten gebruiken wij om vanuit een nieuwe productie site, hoogwaardige voedingsingrediënten te ontwikkelen voor de voedingsmiddelenindustrie in binnen- en buitenland. "Handen uit de mouwen, betrouwbaar en met gezond boerenverstand", geven de grondhouding van Gourmet weer.
"Heb jij oog voor detail en een passie voor perfectie? Als Quality Control medewerker ben jij de laatste kwaliteitscheck voordat onze producten de wereld in gaan, jouw kritische blik maakt het verschil" Ter uitbreiding van ons team zijn wij op zoek naar een nauwkeurige en resultaatgerichte
QC-MEDEWERKER INGREDIENTS
Minimaal 20 uur per week, minimaal 4 dagen, uren flexibel in te delen
JOUW FUNCTIE
- Uitvoeren van kwaliteitscontroles op grondstoffen, halffabricaten en eindproducten.
- Controleren van productiematerialen en het signaleren van afwijkingen.
- Actief meedenken in het verbeteren van processen.
- Rapportage en documentatie van meetgegevens.
- Klantcontact betreffende specificaties en intern specificatiebeheer.
- Ondersteuning productontwikkeling en kwaliteit.
- Beheer monsteraanvragen van aanvraag tot verzending.
JOUW PROFIEL
- MBO werk- en denkniveau.
- (Basis)kennis van HACCP.
- Interesse en/of affiniteit met food & kwaliteit.
- Je hebt bij voorkeur al ervaring op gedaan binnen de levensmiddelenindustrie.
- Je bent zelfstandig en kan ook goed in teamverband werken.
- Goede beheersing van de Nederlandse en Engelse taal.
- Je werkt nauwkeurig, bent proactief en hebt oog voor detail.
- Minimaal 20 uur per week en 4 dagen per week beschikbaar, waaronder de vrijdagen. Verder zijn uren flexibel in te delen.
- Woonachtig in de regio West-Friesland
WORD JIJ ONZE NIEUWE COLLEGA?
Gourmet biedt je een zelfstandige fulltime baan binnen een groeiende, dynamische en innovatieve onderneming. Een prima werksfeer en een team van gemotiveerde collega's.
Herken je jezelf in het bovenstaande profiel ? Aarzel dan niet en stuur je CV naar
Acquisitie naar aanleiding van deze advertentie wordt niet op prijs gesteld.
GOURMET INGREDIENTS BV, SLIMWEG 42, 1614 MG GROOTEBROEK GOURMET.NL
Soort dienstverband: Fulltime, Parttime, Uitzicht op vast, Vaste baan
Contractduur 12 maanden
Arbeidsvoorwaarden:
- Bedrijfsfeesten
- Kerstpakket
- Pensioen
- Reiskostenvergoeding
Werklocatie: Fysiek
Quality Control Specialist
2 dagen geleden geplaatst
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Ensure the highest standards of quality for cutting-edge offshore equipment used in impactful global infrastructure projects.
At IQIP, you’ll ensure we’re building tomorrow’s foundations by assembling, overhauling, and testing advanced equipment used in key infrastructure projects worldwide.
For four decades, IQIP has successfully navigated challenges and built up extensive experience in a wide range of markets, including offshore wind, coastal & civil, offshore oil & gas, and decommissioning.
Who wouldn't want to take part in building the world’s most powerful hydraulic impact hammer? Join a high-tech, hands-on environment where your skills are valued, and growth is part of the journey.
Together, we’ll deliver solutions that make a real, lasting impact.
Your work
As a Quality Control Specialist at IQIP, you are responsible for inspecting and verifying that all materials, components, and final assemblies meet strict quality standards before delivery or deployment. You work closely with manufacturing, engineering, and supply chain teams to ensure compliance with specifications, regulations, and internal procedures. Your role is crucial in safeguarding the reliability, performance, and safety of our high-quality equipment used worldwide in demanding offshore and onshore environments.
Your responsibilities
Perform incoming, in-process, and final inspections of materials and products
Interpret technical drawings and quality specifications
Identify non-conformities and initiate corrective actions in cooperation with other departments
Maintain accurate inspection records and documentation
Support supplier quality assessments and audits
Participate in continuous improvement initiatives to enhance product quality
Ensure compliance with industry standards and safety regulations
Your profile
MBO or HBO education in a technical field such as mechanical engineering or quality management
Experience in a quality control or inspection role, preferably in a technical or manufacturing environment
Knowledge of inspection tools and measurement techniques
Ability to read and interpret technical drawings and documentation
Strong attention to detail and a structured working method
Basic knowledge of ISO standards and quality systems
Good communication skills in Dutch and English
Familiarity with ERP systems is an advantage
What IQIP offers
An opportunity to drive the energy transition with us
Push boundaries to shape tomorrow’s world
Outstanding learning opportunities
Monthly salary depending on your level and expertise
Annual bonus (profit sharing)
8% holiday allowance, paid annually
40 paid annual leave days (27 holidays + 13 additional days)
Benefits such as travel allowance, laptop, and educational opportunities
PME pension fund (CLA/CAO Metalektro applies to this job)
Main working location is Sliedrecht
Flexible working hours
Why IQIP?
We design and manufacture high-quality equipment, tackling challenges through shared expertise and commitment to sustainable solutions. Safety, teamwork, and individual talent power our success as we build a better world for future generations.
Forward Thinking.
Forward Doing. We lead with innovation and integrity. Delivering quality and results.
Global Impact .
Real Challenge. Our projects are challenging and shape the energy and infrastructure landscape of tomorrow.
People First.
Always. You get autonomy, support, and room to grow.
Join us in shaping tomorrow’s world. Click ‘Apply’ and our recruiter will get in touch to get acquainted and answer any questions you may have.
Third Party Manufacturer and Technical Transfer QA Manager- EMEA
2 dagen geleden geplaatst
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**Third Party Manufacturer and Technical Transfer QA Manager- EMEA**
**About Abbott**
Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical science and technology.
**Working at Abbott**
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:
+ A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
+ A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
**The Opportunity**
As **Third Party Manufacturer and Technical Transfer QA Manager,** you'll be responsible for TPM Management and Product Transfer and Technical Support for assigned TPMs.
This position works out of our in Netherland site in the Established Pharmaceutical Division, where we are committed to bringing the benefits of our trusted medicines to more people in the world's fastest-growing countries. Our broad portfolio of high-quality and differentiated branded generic medicines reaches across multiple therapeutic areas including gastroenterology, women's health, cardiometabolic, pain management/central nervous system, and respiratory.
**As the TPM QA Manager, you'll be responsible for:**
+ Providing QA support for assigned TPM's to ensure that safe, efficacious, and quality product can be supplied to Abbott to meet cGMP and other applicable regulatory standards and the appropriate market requirements.
+ Responsible for development of Quality Improvement Plan for TPMs remediations, when required.
+ Managing TPM activities while driving continuous improvement for TPMs.
+ Responsible for Monitoring quality performance for assigned TPMs and ensure requirements per Quality Technical Agreements are adhered / followed by assigned TPMs
+ Leading Quality Technical Agreements approval and periodic review
+ Primary contact for communication of TPM Quality issues as needed.
+ QA support for investigations, trends, complaints, corrective and preventive actions (CAPA), validation support, and product release issues as needed.
+ Responsible for maintaining TPM Approved Supplier Listing.
+ Responsible for supporting Quality Compliance and improvement initiatives.
+ Support new contract manufacturing site approvals must approve all new contract manufacturers for EPD commercial product within responsibility.
+ QA Lead for investigations, trends, complaints, corrective and preventive actions (CAPA), validation support, product release issues, PQR review and change control at TPM sites
+ QA lead for co-ordination with TPMs and internal cross functional team as support and interfaces for routine Quality requirements like GMP audits, new projects or initiatives.
+ Analyzes data, makes decisions or provides recommendations to senior staff regarding quality related issues & crises. Work cross functionally in identifying and resolving technical issues across different EPD regions.
+ Recommends and implements changes to the system as the result of changing regulations and/or business needs.
+ Coordinates across functional areas, business units, and/or geographies in order to achieve the impact goals.
**As Product Technology Transfer QA Manager**
Act as QA Lead for below quality activities during Product Technology Transfer
+ Leading the initiation and implementation of Change Control / Stability and Change Impact Assessment.
+ Test Method Transfer/Analytical Method Validation/Verification.
+ Process Validation/Verification Program
+ First lot quality review for release the validation batches for commercialization.
+ Gather information from the Sending Unit, in order to assemble a data package.
+ Evaluate the information gathered and document findings with respect to product robustness.
+ Participate to the process of creation, approval and continuous improvement of the regulatory documentation related to EPD products. Provide support for the specification setting to Regulatory Affairs and receiving unit.
+ Provide contributions for the Product technical knowledge during and after technology transfer and ensure the product meeting the Quality Standards. Facilitate issue resolution for key investigation and compliance issues
+ Involve in support the quality aspects of the Product Portfolio Expansion, Geographic Expansion initiatives NPI (New Product Introduction) and other Non-Centrally Supported Products.
+ Ensure that projects and technical activities associated with Drug Substances, Drug Products, Intermediates and non-pharma products (food supplement, medical device, cosmetics) are carried out without business interruptions and according to legal and Abbott Quality, Regulatory and business requirements.
+ Liaison between sites QA, commercial affiliates, MS&T (Manufacturing Science and Technology), Operation, Regulatory and other groups as necessary.
+ Serve as quality technical resource of regional EPD Quality organization during process and regulatory deficiency issues, risk assessment target cost initiatives and other continues improvement initiatives.
**Required Qualifications**
+ Bachelor's degree in science , Pharmacy or equivalent level of education at a relevant scientific discipline
+ Minimum 10 years of experience in the pharmaceutical manufacturing field (Quality, production, technical support,etc)
+ Comprehensive understanding of a wide range of Pharmaceutical Manufacturing and Testing Operations
+ Knowledge of international and local quality system and compliance legislations and standards
+ GMP/GLP/GCP background related to medicinal products, medical device, food supplement Biotechnological, Biosimilars and Biologics
+ Good communication and report writing skills in English and French.
+ Strong leadership skills in bringing the best out of people, managing work teams and fostering teamwork within the department.
+ Strong strategic Planning/ Thinking, decisive judgement, and Implementation skills.
+ Flexible for Travel: 30 %
**Preferred Qualifications**
+ Highly skilled on cGMP requirements and Quality Assurance / Quality Control manager for solid, liquid, injectable and biosimilar products.
+ High capabilities in time management, negotiation skills, multi-tasking, communication skills and Microsoft offices.
+ Other qualifications/certifications: IRCA Lead Auditor Certification, Auditor Certification Training, Complaint Certification , GMP-GDP Training. Highly skilled on cGMP requirements, team management, and Quality Assurance / Quality Control manager for solid and injectable products.
Apply Now ( your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
Incoming Quality Control Inspector
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This is a unique opportunity to work as a Incoming Quality Control Inspector with a highly motivated team which is based in Rheden, the Netherlands, to capture the growth opportunities in the renewable hydrogen market!
De functie
Howden Reciprocating and Centrifugal compressors (HCR) is a specialist supplier of tailor-made gas compression equipment to various industries. Our products have made a valuable difference for our clients for the past 100 years, and we are now looking for an Incoming Quality Control Inspector who will join our team and assist us in making a valuable difference in the century to come. The main role purpose is performing defined quality controls in line with weekly plans at Pre-Assembly gate with on time reporting, following all necessary documentation and ensuring cleanliness and necessary care for measurement tools and working area.
- Following HTC Safety 1st policy and reporting of near miss conditions in case.
- Performing planned control activities in line withcompany documentation. Do the necessary Quality call recording with evidence data and report for finding.
- Daily reporting to the departments of Quality (Engineering), Operations Shop, and Operations Planning about the results of the control activities.
- Proper following and reporting of quarantine area in line with our company documentation.
- Supporting and playing an active role for continues improvement studies for our <0 Defect at Shop> principle.
- Proper archiving of inspection evidence data in system.
- Making proposals for improving our products and work processes.
- Participating in team improvement projects.
Over het bedrijf
Howden, a Chart Company / Chart Industries is a leading global manufacturer of highly engineered equipment servicing multiple applications in the clean energy and industrial gas markets. In 2023 Chart Industries acquired the Howden Group, and the entire group is now represented in over 40 countries worldwide with over 11,700 employees. Their vision is to enable the vital processes of our customers and thereby promote a more sustainable world. Learnmore about them at .
Aanbod
You will get the chance to develop and realize new improvements, have quality discussions, and celebrate successes in a team with a good atmosphere and dedicated colleagues. In this role you will truly have high responsibility and accountability in a global presence. As we consider talent management as key to the success of our organization, we offer opportunities for personal and professional development. We offer a salary package that is fully in line with the level of the position combined with an extensive package of fringe benefits.
Jouw profiel
- Background knowledge and experience in Dimension Control and Visual Control.
- Experience in measurement tools.
- Knowledge of international regulations and quality processes is preferred.
- A practical and pro-active personality that shows a strong sense of ownerships and a customer focus.
- A team player with a willingness to learn and develop with a continuous improvement mindset.
- Makes decisions with regards to conformity of the activity or of the controlled item.
- Good communication skills in English and Dutch.
- Ability to read and to understand documentation in English, and drawings of mechanical parts (2D & 3D), including tolerances, P&I diagrams.
Wees de eerste die het weet
Over het nieuwste Qa manager Banen in Nederland !
Chemisch Analist Quality Control
2 dagen geleden geplaatst
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Functieomschrijving
Heb jij recent een MBO-4 of HBO-opleiding afgerond in bijvoorbeeld Chemie, Chemisch-Fysisch Laboratoriumonderzoek, Life Sciences of een soortgelijke studierichting? Ben je op zoek naar je eerste echte baan waarin je praktijkervaring kunt opdoen in een professioneel laboratorium? Dan hebben wij een mooie kans voor jou!
Bent u de juiste sollicitant voor deze functie? Ontdek het door het functieoverzicht hieronder te lezen.
Functieomschrijving
In deze rol als Laborant binnen de kwaliteitscontrole zorg jij ervoor dat producten en grondstoffen voldoen aan de gestelde kwaliteitseisen. Je werkt nauwkeurig en voert analyses uit volgens vastgestelde richtlijnen. Dit alles vindt plaats binnen sectoren als de voedingsmiddelenindustrie, chemische sector, farmacie of materiaalkunde.
Verantwoordelijkheden:Uitvoeren van chemische en fysische analyses zoals ICP, XRF, HPLC en GC-MS
Kalibreren van meetapparatuur en registreren van data in SAP/LIMS
Assisteren bij het verbeteren en valideren van analysemethoden
Op termijn mogelijkheid om je te specialiseren in het behandelen van klantklachten
Je hebt een afgeronde MBO-4 of HBO-opleiding op het gebied van chemie of laboratoriumtechniek
Je hebt laboratoriumervaring opgedaan via stage of eerdere werkervaring
Je werkt nauwkeurig, bent kritisch op kwaliteit en wilt graag nieuwe dingen leren
Je woont in de regio Ede of Wageningen, of bent bereid hierheen te reizen
Salaris tussen de €2.600 en €.200 per maand (afhankelijk van je ervaring)
Vaste aanstelling
Reiskostenvergoeding van 23 per kilometer
Vakantie en verlof: 25 vakantiedagen én 13 ADV-dagen
Goede pensioenregeling
- Werklocatie in de omgeving van Wageningen
- Vacaturenummer 26466
Chemisch Analist Quality Control
Vandaag
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Functieomschrijving
Heb jij recent een MBO-4 of HBO-opleiding afgerond in bijvoorbeeld Chemie, Chemisch-Fysisch Laboratoriumonderzoek, Life Sciences of een soortgelijke studierichting? Ben je op zoek naar je eerste echte baan waarin je praktijkervaring kunt opdoen in een professioneel laboratorium? Dan hebben wij een mooie kans voor jou!
FunctieomschrijvingIn deze rol als Laborant binnen de kwaliteitscontrole zorg jij ervoor dat producten en grondstoffen voldoen aan de gestelde kwaliteitseisen. Je werkt nauwkeurig en voert analyses uit volgens vastgestelde richtlijnen. Dit alles vindt plaats binnen sectoren als de voedingsmiddelenindustrie, chemische sector, farmacie of materiaalkunde.
Verantwoordelijkheden:Uitvoeren van chemische en fysische analyses zoals ICP, XRF, HPLC en GC-MS
Kalibreren van meetapparatuur en registreren van data in SAP/LIMS
Assisteren bij het verbeteren en valideren van analysemethoden
Op termijn mogelijkheid om je te specialiseren in het behandelen van klantklachten
Je hebt een afgeronde MBO-4 of HBO-opleiding op het gebied van chemie of laboratoriumtechniek
Je hebt laboratoriumervaring opgedaan via stage of eerdere werkervaring
Je werkt nauwkeurig, bent kritisch op kwaliteit en wilt graag nieuwe dingen leren
Je woont in de regio Ede of Wageningen, of bent bereid hierheen te reizen
Salaris tussen de €2.600 en €.200 per maand (afhankelijk van je ervaring)
Vaste aanstelling
Reiskostenvergoeding van 23 per kilometer
Vakantie en verlof: 25 vakantiedagen én 13 ADV-dagen
Goede pensioenregeling
- Werklocatie in de omgeving van Wageningen
- Vacaturenummer 26466
Chemisch analist quality control
Vandaag
Taak bekeken