research and development vacatures

In de buurt zuid holland
242Banen gevonden

242 vacatures gevonden voor research and development vacatures In de buurt zuid holland

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RA Coordinator

CLS Services B.V.

Leiden, ZH
3 dagen geleden
Leiden, ZH
3 dagen geleden
CLS Services is a leading professional recruitment agency, specialised in the recruitment and career coaching of people with a background in chemistry & life sciences. For our client, Astellas Pharma Europe B.V. (Leiden, Nederland), we are searching for a RA Coordinator.


Keywords
  • Regulatory Affairs
  • Pharmaceutical experience
  • International market
  • Strategy development


Profile
As part of a Global Project, you will act as a Regulatory Affairs Project Coordinator. Driven by Commercial having an impact on the registered portfolio in Astellas International Markets. The markets include 47 countries across Latin America, Middle-East Africa, Russia-CIS, and Asia
Main Tasks:
  • Develop the regulatory strategy and planning to support the commercial strategy in the selected countries, which may imply MA discontinuation and/or implementation of alternative access models when applicable;
  • Coordinate its execution in collaboration with other functions (incl. Commercial, Supply Chain, QA, PV, Medical Affairs, Legal) and in line with Astellas SOPs.

Who we're looking for
The ideal candidate has at least a bachelor’s degree in scientific discipline and at least 5-8 years previous experience with regulatory affairs in the pharmaceutical industry, preferably with International Markets. You have strong organizational skills with the ability to manage large projects and provide regulatory guidance/training to internal stakeholders and others in the department as needed. Project leader experience is required.
Other requirements:
  • Excellent communication and writing skills (advise, convince, negotiate, listen, present and edit);
  • Ability to communicate effectively with cultural awareness and sensitivity and maintain effective working relationships;
  • Experience in working in multidisciplinary teams;
  • High integrity with respect to maintenance of proprietary, confidential information;
  • Fluent in English, both spoken and written.

Company profile
Astellas is a Japanese multinational pharmaceutical company employing over 17,000 people worldwide with global sales exceeding 11 billion euro. The group’s EMEA headquarters are based in London, with affiliates throughout Europe engaged in research & development (R&D), manufacturing and sales & marketing. With over 4,500 employees, EMEA is an important and growing Astellas region, having key strengths in the therapy areas of Urology, Transplantation, Anti Infectives, Pain Management and Oncology. The global annual R&D investment of 15% to 20% of sales is evidence of the group’s commitment to improving the health of people worldwide through the provision of innovative and reliable products. Astellas employs around 950 persons in the Netherlands, in Leiden and Meppel.


Additional vacancy information
Reference:A2100043
Contract:Temporary contract with CLS Services
Education:HBO/BSc.
Employment terms:Contract for 3 - 4 days per week
Salary: >5500
Days of leave: 25 + 13
See here our other employment terms for this vacancy
Publication date:1-3-2021
Location:View location with Google Maps
Contactperson:Aniek Vugts
+31 (0)31 (0)88 22 77 555

Apply
Please apply online here for this job (Job Ref: A2100043). You can also check our other vacancies. You can also follow us on Twitter.
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Quality Systems Document Control Associate

CLS Services B.V.

Leiden, ZH
8 dagen geleden
Leiden, ZH
8 dagen geleden
CLS Services is a leading professional recruitment agency, specialised in the recruitment and career coaching of people with a background in chemistry & life sciences. For our client, Astellas Pharma Europe B.V. (Leiden, Nederland), we are searching for a Quality Systems Document Control Associate .


Keywords
  • Quality Documents
  • SOP's
  • Excel experience
  • Independant worker
  • Contact with customers


Profile
In your role as Quality Systems Document Control Associate you are responsible for the development and maintenance of the Quality Management System (QMS) Document Control system supporting Regulatory Affairs, Pharmacovigilance, Development, Medical Affairs, and other functions that utilize the Medical and Development QMS. You will contribute to the development, implementation, and successful execution of the CRQA mission, objectives and 3-5 year strategic plan.
Responsibilities:
  • Function as the Quality Document (QD) Administrator responsible for reviewing new or revised Quality Documents for compliance to established standards;
  • Ensure all Quality Documents meet required standards before processing documents in the Astellas Document Management System - Quality Document (ADMS QD) workflows;
  • Ensure impacted stakeholders are involved in the review of new and revised Quality Documents;
  • Deliver effective communication of requirements and standards to Authors of Quality Documents as well as to the Users of the Astellas Document Management System - Quality Document (ADMS QD);
  • Support the development, review and delivery of training materials to provide to new users of the ADMS QD system;
  • Provide guidance on proper methods for writing SOPs and other Quality Documents to meet standards;
  • Support Document Control initiatives that lead to process improvements;
  • Respond to email inquiries and user support questions;
  • Support ADMS QD users on document retrieval for superseded and obsolete documents as well as completing requests for uploading documents into the ADMS QD Repository.

Who we're looking for
We are looking for an enthusiastic candidate with a Bachelor degree with some experience in the pharmaceutical industry. Preferable, you have experience within Quality Assurance and/or within SOP writing, Process Improvement or similar discipline. You are proficient in working with Microsoft Microsoft Office tools (e.g., Word, Excel, PowerPoint) and PDF editor software (e.g., Adobe Professional, Foxit).
Because of the intercontinetal team, it is important that you are a self-starter and that you can work independantly. Excellent communication skills are a must. You can multitask and shift workload according to the department/team priorities and you have strong planning and organizational skills.


Company profile
Astellas is a Japanese multinational pharmaceutical company employing over 17,000 people worldwide with global sales exceeding 11 billion euro. The group’s EMEA headquarters are based in London, with affiliates throughout Europe engaged in research & development (R&D), manufacturing and sales & marketing. With over 4,500 employees, EMEA is an important and growing Astellas region, having key strengths in the therapy areas of Urology, Transplantation, Anti Infectives, Pain Management and Oncology. The global annual R&D investment of 15% to 20% of sales is evidence of the group’s commitment to improving the health of people worldwide through the provision of innovative and reliable products. Astellas employs around 950 persons in the Netherlands, in Leiden and Meppel.


Additional vacancy information
Reference:A2100040
Contract:Temporary contract with CLS Services
Education:HBO/BSc.
Employment terms:Salary: max 2700
Days of leave: 25 + 13
See here our other employment terms for this vacancy
Publication date:24-2-2021
Location:View location with Google Maps
Contactperson:Aniek Vugts
+31 (0)31 (0)88 22 77 555

Apply
Please apply online here for this job (Job Ref: A2100040). You can also check our other vacancies. You can also follow us on Twitter.
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Affiliate Support Manager

CLS Services B.V.

Leiden, ZH
3 dagen geleden
Leiden, ZH
3 dagen geleden
CLS Services is a leading professional recruitment agency, specialised in the recruitment and career coaching of people with a background in chemistry & life sciences. For our client, Astellas Pharma Europe B.V. (Leiden, Nederland), we are searching for an Affiliate Support Manager.


Keywords
  • Pharmacoviliance
  • Drug Safety Officer
  • Regulatory (regional / global)
  • Excellent communication
  • Problem solver


Profile
In this role, you are responsible for the day-to-day interactions with the Affiliate Drug Safety Officers (DSO) to ensure all Affiliate local PV systems, processes and procedures are compliant, efficient and in line with global/regional regulatory requirements and Astellas policies and procedures.
You will have frequent interactions with DSOs, Affiliates colleagues, DSO/Affiliate Management, QPPV, PVQA colleagues so excellent communication skills and building good relationships are key.
Responsibilities:
  • Serve as first point of contact for all DSOs, globally;
  • Monitor affiliate performance and oversees training of Affiliate staff;
  • Ensure audit and inspection readiness of Affiliates;
  • Develop, oversee and implement (associated) CAPAs as the performance of the PV Affiliates has a direct impact on the Astellas PV system and compliance;
  • Develop and review regional QDs for consistency with regional/global regulatory requirements, SOPs and Astellas' expectations;
  • Ensure delivery of training to DSOs;
  • Monitor DSO performance based on predefined KPI;
  • Initiate and manage process improvement projects related to Affiliate procedures;
  • Ensure training requirements for DSOs are kept up to date;
  • Interact with DSO and other staff for implementation of PV-related regional and/or global procedures.

Who we're looking for
The ideal candidate has a BSc. or MSc. degree and at least 5 years of relevant experience. We are looking for a technical expert with an in-depth understanding of all aspects of PV and related disciplines. You have a strong industry mindset and are willing to travel up to 50% (after Covid).
You like to solve complex problems in a creative way and communicates excellent with partners and different departments.
Are you the experienced PV candidate we are looking for?


Company profile
Astellas is a Japanese multinational pharmaceutical company employing over 17,000 people worldwide with global sales exceeding 11 billion euro. The group’s EMEA headquarters are based in London, with affiliates throughout Europe engaged in research & development (R&D), manufacturing and sales & marketing. With over 4,500 employees, EMEA is an important and growing Astellas region, having key strengths in the therapy areas of Urology, Transplantation, Anti Infectives, Pain Management and Oncology. The global annual R&D investment of 15% to 20% of sales is evidence of the group’s commitment to improving the health of people worldwide through the provision of innovative and reliable products. Astellas employs around 950 persons in the Netherlands, in Leiden and Meppel.


Additional vacancy information
Reference:A2100029
Contract:Temporary contract with CLS Services
Education:WO/MSc.
HBO/BSc.
Employment terms:Salary: >3500
Days of leave: 25 + 13
See here our other employment terms for this vacancy
Publication date:12-2-2021
Location:View location with Google Maps
Contactperson:Aniek Vugts
+31 (0)31 (0)88 22 77 555

Apply
Please apply online here for this job (Job Ref: A2100029). You can also check our other vacancies. You can also follow us on Twitter.
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PV Compliance Manager

CLS Services B.V.

Leiden, ZH
8 dagen geleden
Leiden, ZH
8 dagen geleden
CLS Services is a leading professional recruitment agency, specialised in the recruitment and career coaching of people with a background in chemistry & life sciences. For our client, Astellas Pharma Europe B.V. (Leiden, Nederland), we are searching for a PV Compliance Manager.


Keywords
  • Pharmacovigilance
  • Safety Database
  • Root Cause Analysis
  • Audit/inspection


Profile
As (Associate) PV Compliance Manager, you will assist with the continuous monitoring of PV compliance, submission timeliness and quality metrics, including detection of negative patterns and trends, in close collaboration with internal and external stake holders (Regulatory Affairs, Quality Assurance, Business Partners). You support the preparation of PV metrics reports and presentations that include performance indicators that provide feedback to functional PV groups. You will work in close contact with people in the US, EU and Japan, and you will represent the compliance team during audits/inspections, mostly via telephone or video.



Who we're looking for
The ideal candidate has 3-6 years of experience in Pharma Quality and/or Compliance. You should have experience with Pharmacovigilance, PV Safety Databases, case processing and with performing Root Cause Analysis. As you will represent the Compliance team during audits and inspections, relevant experience is also a necessity. We are looking for someone who is a good listener and has strong communication and presentation skills. Are you the pro-active team player we are looking for?

Company profile
Astellas is a Japanese multinational pharmaceutical company employing over 17,000 people world-wide with global sales exceeding 11 billion euro. The group’s EMEA headquarters are based in London, with affiliates throughout Europe engaged in research & development (R&D), manufacturing and sales & marketing. With over 4,500 employees, EMEA is an important and growing Astellas region, having key strengths in the therapy areas of Urology, Transplantation, Anti Infectives, Pain Management and Oncology. The global annual R&D investment of 15% to 20% of sales is evidence of the group’s commitment to improving the health of people world-wide through the provision of innovative and reliable products. Astellas employs around 950 persons in the Netherlands, in Leiden and Meppel.


Additional vacancy information
Reference:A2100039
Contract:Temporary contract with CLS Services
Education:HBO/BSc.
WO/MSc.
Employment terms:Salary: 3500 - 5000
Days of leave: 25 + 13
See here our other employment terms for this vacancy
Contract for at least 1 year, with the option to extend yearly.
Publication date:24-2-2021
Location:View location with Google Maps
Contactperson:Aniek Vugts
+31 (0)31 (0)88 22 77 555

Apply
Please apply online here for this job (Job Ref: A2100039). You can also check our other vacancies. You can also follow us on Twitter.
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Laboratory Technician Cell Biology

Dümmen Orange The Netherlands B.V.

De Lier, ZH
6 dagen geleden
De Lier, ZH
6 dagen geleden

Dümmen Orange is the world’s largest breeder and propagator of cut flowers, bulbs, tropical plants, pot plants, bedding plants and perennials. For our Research & Development department, section Cell Biology & Tissue Culture, in De Lier we are looking for a Laboratory Technician Cell Biology.
Job objective
Our organization grows and flourishes. This results in a fast-changing and, therefore, challenging environment.

As Laboratory Technician you will actively participate in routine Tissue Culture activities within our Technology Application domain. The position offers exposure to the state-of-the-art cell biology and tissue culture technologies applied to a wide variety of ornamental crops in a competitive and dynamic environment. You will actively take part in a young and dynamic team; good communication skills and team-player mentality are valued in all our lab personnel. The reporting line is directed to Team Lead In Vitro.

Your tasks and responsibilities
You will have the following responsibilities and will perform the associated tasks to fulfil them:
•    Efficient and timely execution of routine activities like media preparation, multiplication and maintenance of stock plants, shipment etc;
•    Take part in processing different running projects e.g. embryo rescue, meristem culture, organogenesis;
•    Following process guidelines to achieve the best quality;
•    Assisting with Protocol applications and process execution;
•    Verbal and written report on progress;
•    Initiation of diagnostic testing by preparing and sending samples to diagnostic laboratory;
•    Supporting the Technology Application team with planning, organization, communication and administration.
Your profile
•    Vocational (or B.Sc.) degree in Life Sciences and/or Laboratory applications;
•    Proven experience with several of the techniques described above. Plant tissue culture experience is a plus;
•    Excellent interpersonal and communication skills;
•    Team player mentality;
•    Excellent command of the Dutch and English language.
We offer
Dümmen Orange has great global ambitions. Innovation, technology and quality are high priorities. This results in a challenging working environment in which you can develop yourself. Dümmen Orange offers its employees plenty of room for personal growth and development. We have an informal and easy accessible working environment in which cooperation is very important.
Dümmen Orange  
Dümmen Orange is the world’s largest breeder and propagator of flowers and plants. Its annual turnover is about 350 million euro. The company employs over 7.300 employees worldwide. In addition to a large marketing and sales network, Dümmen Orange has a diversified network of specialized production sites. The key to Dümmen Orange’s success is a broad and deep product range, supported by a global supply chain. The company embraces its social responsibilities and invests in the health, safety and personal development of its staff.

Your application
Click on the button below to apply for this job. If you have questions about the job, you can contact Mehdi Massoumi (Team lead In Vitro), via +31 174 540 100.   

Acquisition with reference to this advertisement will not be appreciated.

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R&D Manager

Koster en Van Kooten

Rotterdam, ZH
Vandaag
Rotterdam, ZH
Vandaag

R&D Manager

Our client is a company seen as an expert in our specific niche of diagnostics systems for factory and process automation applications. We have 22 years’ experience with deep level protocol analysis via our hardware and software solutions. In our space, we are seen as innovation leaders. We are typically the first to bring ideas and concepts to market. We are seeking new talent to continue this exciting successful journey.

The talent we are seeking are individuals who are motivated for delivering on the promise of Industry 4.0/IIOT to industries that maybe considered late adaptors. You should be motivated to bring these new concepts and ideas to older systems, mixed protocol architectures, and push the limits pasts what originally considered for these systems. You will have the opportunity to work with experts in factory and process networks. This includes working with direct market feedback, to deliver on the promise we make to our stakeholders. We expect innovators to be encouraged to unlock their potential by everyday coming to work with the concept of “what can I do today to make a field technician’s network communications operate better?“

Our process is in a modified Agile method, applied via our tools such as ARM hardware, Linux Centos, C++, and Angular. We have internal processes centered around mentorship, access to regular feedback, and quick deliverables. We work in small teams with roadmaps developed with making sure individuals have space to place their mark on what we do. We aim to support the innovators, the goal oriented, and those looking to make differences in industrial applications. 

At the moment, our development team is seeking a R&D Manager.

The role

As our R&D manager, you must have a passion and focus on seeing developers grow and results driven roadmap delivery. Your mindset should be that continuous improvement mindset and execution is a requirement to how we intend to rise to our clients expectations. After you deliver improvements on our processes, backlog and developer growth, we want you to grow into a larger role with our innovation process and external market perception. Growth in your role, first comes after delivering on ideas with being action-oriented personality.  

You have an excitement for leading a team that works toward solving the challenges or field technicians globally. 

Furthermore you will be responsible for managing a backlog of items, getting enjoyment from knowing these items are driven by client feedback. Last, you like to sit with clients, research, and improve their knowledge about our industry so they can place their innovative ideas on the roadmap over time. 

  • Continuous improvement mindset of “Plan, Do, Check, Act”
  • Ability to do research on best practices and develop effective plans to improve processes
  • Ability to quickly connect with different personality types, and create trust toward getting results on the task(s) on hand.
  • Plan and delivery of projects or agreed upon strategy on time.
  • Manage backlog of maintenance user stories that are client driven
  • Delivering on actions necessary to commercial launch the developed solutions.
  • Coordinating Scrum meetings and events, such as: Production management meetings, Sprint Reviews, Sprint Planning, Retrospective, Backlog Refinement meetings
  • Meet with stakeholders to understand their needs, wishes and possible complaints with regards to our products
  • Interact with other stakeholders on the management team
  • Guard our roadmap during the product development phase
  • Attend release events, to represent our R&D and network
  • Give input and possible content creation for marketing purposes
  • Passion for field technicians in factory and process automation, including respect for what they do and solving their challenges.

What we are looking for:

  • Bachelor working and thinking level
  • Experience in leading a (multi-disciplinair) team
  • Experience in mentoring engineers in their career path
  • Knowledge of embedded software and hardware solutions
  • Analytic and self-critical
  • You have an up-to-date knowledge of PROFIBUS (a pro);
  • You have an interest in Industrial Automation;
  •  Excellent verbal and writing skills in English and Dutch.

Capable of delivering under pressure

Our offer:

  • Full-time position (40 hours) for a longer period;
  • Good salary and secondary employment conditions;
  • A varied position with room for your ideas;
  • Personal and professional development;
  • Lease car, laptop and mobile phone;
  • An international team of highly driven professionals in an informal working environment.
Interested?
Please send your application (resume and motivation) to jan@kosterenvankooten.nl or call at 06-24288598 for more information. You can use the apply button to send your resume and motivation. 

 

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Project: Scientist Analytical Development (100% remote within EMEA)

Oxford Global Resources

Leiden, ZH
9 dagen geleden
Leiden, ZH
€4.2k - €5.8k Per maand
9 dagen geleden
€4.2k - €5.8k Per maand

Are you a person with passion for Analytical Chemistry? Do you have extensive experience with HPLC/UPLC, dissolution and other major analytical techniques? This is a phenomenal opportunity for you!
Job Description
For our client Johnson & Johnson Consumer Products, a member of Johnson & Johnson's Family of Consumer Companies,we are recruiting for a Principal Scientist. The Analytical Lifecycle Management team is responsible for J&J OTC products worldwide. The principal scientist will work within the analytical section and support marketed OTC products primarily within EMEA/APAC but also globally. You will be in a regional team of 6 analytical colleagues and you will report to an Associate Director. This role can be filled 100% remote, but you will have extensive everyday contacts with external and internal manufacturers, CROs and J&J colleagues all over the world.
Responsibilities
  • Together with your colleagues you will provide desktop analytical support for a series of projects associated with the currently marketed OTC products. Technical support will include but not be limited to:
  • Supporting analytical test method trouble shooting;
  • Supporting analytical test method improvement and validation;
  • Supporting analytical test method transfers;
  • Managing CROs and other external partners;
  • Managing change control deliverables and CAPA activities relating to analytical testing and transfers;

Requirements
  • Minimum of Master of Science within a relevant chemistry or pharmaceutical area;
  • 5 + years of experience in an analytical laboratory role with a major emphasis on analytical method development, optimization and product testing;
  • Demonstrated experience and deep knowledge within HPLC/UPLC, dissolution and other major analytical techniques;
  • Able to grasp, understand and translate complex problems into explicit work packages;
  • Since the product portfolio is global, a broad knowledge of worldwide requirements is a plus. Activities are, to a large extent, outsourced and experience in working with contract development/research organizations is a merit;
  • Eligible to work in EMEA region (work permit) is a must;
  • Experience with working with external sites and on remote basis;
  • Available on short notice;

Benefits
  • Contract: via Oxford, ZZP is also a possibility;
  • Duraton: This is a project based role; expected duration is untill end-of year
  • Salary: €4200- €5800 gross monthly based on a full-time position
  • Holidays: 25
  • Working hours: full-time, day shift.
  • Region: EMEA
  • Vacancy number: 17062

Oxford Global Resources is het grootste recruitmentbureau binnen de vakgebieden Science, Engineering en IT. Al onze recruiters hebben zelf een relevante achtergrond binnen deze gebieden en helpen je graag bij het vinden van de perfecte baan in ons uitgebreide netwerk.
Als gespecialiseerde partij hebben wij een groot aanbod aan laboratorium vacatures op het gebied van Quality Control (QC) en Research &Development (R&D) binnen diverse sectoren, waaronder de Farmaceutische industrie, Biotechnologie, Contract Manufacturing, Contract Research, Voedingsmiddelenindustrie, Chemie, Milieu en Plantensector.
Oxford is altijd op zoek naar talent met expertise op het gebied van Biotechnologie, Immunologie, Biochemie, Virologie, Microbiologie, Moleculaire Biologie, Life Science, Analytische Chemie, Fysische Chemie, Polymeerchemie, Petrochemie en Diagnostiek. Wij komen graag in contact met kandidaten die ervaring hebben met een of meerdere van de volgende technieken: USP (Upstream Processing) DSP (Downstream Processing), Bioprocesses, viruskweek, celkweek, ELISA, FACS, Western Blot, SDS-page, PCR, RT-PCR, qPCR, kloneren, sequencing, eiwit zuivering, purificatie, HPLC, UPLC, chromatografie, fysische chemie, viscositeit, smeltpunt, pourpoint, pH, XRF, GC, GC-MS, LC, LC-MS, ICP ICP-MS, AAS, UV, titraties, Karl Fisher, formuleren, steriliteit, determinaties, bioburden, environmental monitoring, LIMS, GMP, GLP, GCP, GDP, ISO17025.
Vind je deze vacature interessant? Of ben jij op zoek naar een functie op MLO, HLO, BSc, WO, MSc of PhD en heb je interesse in de vacature laboratorium Assistent, Laborant, Laborant monstervoorbereiding, Analist, Technician, Assistant Scientist, Associate Scientist, Scientist, Manufacturing Specialist, Process Engineer, Validatie Engineer, QA (Quality Assurance) Officer, RA (Regulatory Affairs) Officer, Supervisor, Teamleider, Afdelingshoofd, Hoofd Laboratorium, Manager, Director, etc. Neem dan direct contact met ons op!
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Assistant Scientist - R&D (DSP, pharma)

Oxford Global Resources

Leiden, ZH
23 dagen geleden
Leiden, ZH
€2.4k - €3.1k Per maand
23 dagen geleden
€2.4k - €3.1k Per maand

Are you looking for a new challenge in a DSP and R&D setting within the pharmaceutical industry? Are you keen on working with state of the art technology and do you want to develop new processes? We might have what you are looking for!
Job Description
At this site our client develops best-in-class vaccines for some of the world's most life-threatening infectious diseases. They have built a dedicated, world-class, multi-functional team across a variety of disciplines to develop a promising vaccines pipeline.
Process development consists of two divisions: USP and DSP. Together they are responsible for the development of scalable production processes for vaccines. It is important that these new processes are safe, trustworthy, scalable, cost-effective and, most importantly, are according to GMP-guidelines. The developed production processes are transferred into GMP production facilities for the production of clinical batches and scaled-up for commercial production.
We are looking for a motivated Assistant Scientist within the field of downstream process development (DSP) within R&D.
Responsibilities
  • Plan, prepare and execute scientific studies.
  • Use techniques such as filtration, chromatography and UF/DF.
  • Perform experiments on pilot scale or in reduced-scale models

Requirements
  • You have at least a BSc / MSc degree in the life science field.
  • You work accurately and are a team player with excellent communication skills.
  • It would be a plus if you are already familiar with DSP techniques

Benefits
  • Contract: 1 year through Oxford Global Resources, realistic long term perspective
  • Salary: €2400,- till €3100,- gross monthly based on level of experience;
  • Hours full-time preferred 32h discussable.
  • Startdate: as soon as possible;
  • Vacancy number: 16925

Oxford is always looking for talent with expertise in Biotechnology, Immunology, Biochemistry, Virology, Microbiology, Molecular Biology, Life Science, Analytical Chemistry, Physical Chemistry, Polymer Chemistry, Petrochemistry and Diagnostics. We are keen to meet candidates who have experience in one or more of the following techniques: USP (Upstream Processing) DSP (Downstream Processing), Bioprocesses, virus culture, cell culture, ELISA, FACS, Western Blot, SDS-page, PCR, RT-PCR, qPCR, cloning, sequencing, protein purification, purification, HPLC, UPLC, chromatography, physical chemistry, viscosity, melting point, pourpoint, pH, XRF, GC, GC-MS, LC, LC-MS, ICP ICP-MS, AAS, UV, titrations, Karl Fisher, formulation, sterility, determinations, bioburden, environmental monitoring, LIMS, GMP, GLP, GCP, GDP, ISO17025.
Do you find this vacancy interesting? Or are you looking for a position at MLA, HLO, BSc, WO, MSc or PhD and are you interested in the vacancy laboratory Assistant, Laboratory Assistant, Sample Preparation Laboratory Assistant, Analyst, Technician, Assistant Scientist, Associate Scientist, Scientist, Manufacturing Specialist, Process Engineer, Validation Engineer, QA (Quality Assurance) Officer, RA (Regulatory Affairs) Officer, Supervisor, Team Leader, Department Head, Laboratory Manager, Manager, Director, etc.? Please contact us directly!
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Mendix Developer

Mendix

Rotterdam
30+ dagen geleden
Rotterdam
30+ dagen geleden
Mendix is on a mission to enable anyone in any organization – from the marketing coordinator to the software developer to the CEO – to create things that are transformational for their company.  We are fundamentally reinventing the way applications are created and we’re reinventing the future of software development.  Sounds ambitious, right?  We agree.

Not to brag, but nearly 4,000 organizations worldwide, including KLM, Medtronic, Merck, and Philips, rely on Mendix to build web and mobile applications.  Thousands of our customers use our platform to delight their clients and empower their employees. It’s no surprise that we’re a recognized Leader by Gartner and Forrester in a red-hot market expected to exceed $21 billion by 2022.  Ok, maybe we did want to brag a little.  But we’re proud of what we’ve accomplished…and…we’re humble enough to admit that we need you to make us even more effective.

The Mendix AppFactory is a team of Mendix Makers, with a focus on building applications with our own Mendix platform. In other words: for Mendix with Mendix! 
These applications vary in nature from improving business processes, facilitating R&D innovations, building industry solutions, cross-industry components and showcasing the power of Mendix at our events.

Not only is the Mendix AppFactory turning ideas into Mendix Apps, we are also a breeding ground for Mendix talent. We are on a mission to produce great Mendix apps and even better Mendix Makers! 

As a Mendix Developer, you will be a part of this endeavor. Helping out people from within our company to realize their ideas into smoothly running and user-friendly applications, putting a smile on people’s faces as you make their job easier to do! You will be in a unique position, that allows you to learn a lot about Mendix: how to create better apps, but also how different departments within the company operate, or help out building complete solutions with Mendix. You will also be instrumental in setting up new and testing existing guidelines and digital execution practices. 
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Algorithm Developer - C# C++

Zealogics.com

Delft, ZH
30+ dagen geleden
Delft, ZH
30+ dagen geleden

Job Title: Algorithm Developer - C# C++

Location: Delt - Netherlands 

Type: Contract

C++ Developer / Senior C# Software Engineer (Image Processing R&D C++ C#). Senior C++ Developer with a broad range of technical knowledge including C++ and C#.

You will design and develop algorithms and produce prototypes for researchers within a R&D environment.
As a Senior C++ Developer you will work throughout the full development lifecycle on both embedded and user interface code on Windows, utilising C++, C# and WPF.
This role would suit an ambitious Senior Algorithm Developer eager to grow into a technical team lead as the company expands.
Requirements:
Extensive software development experience with C++ (ideally including STL) and C#
Strong multi-threading skills
Experience with real-time or embedded software
Thorough understanding of computing fundamentals such as Object Orientated Programming, algorithm design
Excellent written and verbal communication skills
Degree educated, mathematics or computer science preferred
Desirable: understanding of image processing algorithms such as filtering, blob detection, binary morphology

Type functie

Fulltime, Parttime

Geplaatst op

3 dagen geleden