Operational Coordinator International Transport (ENG).
PostNL
Leidschendam, ZHOperational Coordinator International Transport (ENG).
- Leidschendam
- HBO/WO
- Logistiek
- Professional
Wat ga je doen?
As Operational Coordinator International Transport you are responsible for the coordination of all road transport in Europe, including: order management, purchasing, operation, performance management, relationship management and Back Office. You are the first point of contact for our internal & external clients in need of road transportation (FTL/LTL) within Europe. Therefore you collaborate with a selected network of transport partners which are commissioned by our department to fulfil these needs. You also monitor this process regarding both quality and cost and are responsible for the correct administrative handling in our systems. Your most important tasks are: purchase, coordinate with stakeholders and transport partners and organize the implementation of these services. Your most important KPI’s are: cost and performance.
At the Operational Partnerships & Linehaul department we are a team of 16 driven professionals. You work closely together with two other Operational Coordinators International Transport and the Senior Coordinator International Transport. We are part of Cross Border Solutions (CBS), the business unit that provides tailor-made delivery solutions to businesses worldwide under the Spring brand. We deliver special moments to everyone and everywhere.
Onze ambitie
We want to be the preferred logistics solutions provider by delivering special moments every day. Our employees and customers are key. We are always looking for ways to be better. As a result, we need you to act as specialist to your stakeholders regarding road transport requests and issues related to this service. We are looking for someone that knows how to help us increase our performance levels through the optimization of both process and data.
Wat breng jij mee?
- MBO+ or HBO (bachelor) diploma in Logistics or Transportation and at least 3-5 years related work experience in international logistics or e-commerce.
- Good understanding of Cross Border business processes and IT solutions.
- Demonstrated experience with Excel, Power BI and data analysis.
- Excellent English and Dutch written and verbal communication skills. Knowledge of another European language is highly desirable.
You have a no-nonsense mentality and a practical approach. You are an excellent problem solver with a proactive and results oriented attitude. You are good at relationship management and know how to keep an overview when doing many things at the same time. You don’t get easily stressed or frustrated when confronted with the unexpected. Please note that to qualify you need to have all relevant and valid working entitlements (visa/work permit) and must currently reside in The Netherlands.
Wat bezorgen we jou?
- Gross salary indication between € 2.600 and € 3.900 based on 39,25 hours a week (level 8 of the PostNL Collective Labour Agreement).
- Laptop and smartphone.
- Room for growth and for personal development.
- Work location: The Hague Forepark at the International Mail and E-commerce Center (IMEC).
- For further information on our attractive terms of employment please click here.
We offer you a far-reaching and meaningful job. Your solutions, ideas and smart plans have a direct impact on millions of customers around the world. Including you!. We provide a motivating work environment that allows you to develop professionally. Together we are shaping the future of e-commerce.
Interested?
PostNL wants to be everyone’s favorite logistics company. Therefore everyone is welcome to join us. Where you were born, what you believe in and who you love is irrelevant to us. We care only about your unique talent. Pay close attention to the above requirements and explain clearly in your application, and with specific examples, why you are the right person for this role.
You can apply for this position with your resume and cover letter until March 12, 2021 before 9 a.m. On March 16, 2021 we will advise you on the status of your application. A Certificate of Conduct(VOG) and pre-employment screening are part of the selection process.
The video job interviews are planned for March 23, 2021. If you are not available on this date, please let us know in advance.
Sollicitatieproces
1. Sollicitatie
Bedankt voor je sollicitatie! Je krijgt binnen vijf werkdagen een reactie van onze recruiter.2. Telefonisch contact
Hebben we vragen over je CV of motivatie, dan bellen we je.3. Gesprekken
Afhankelijk van de functie heb je één of meerdere gesprekken met onze recruiter, je toekomstige manager en directe collega’s. In verband met het coronavirus voeren we dit gesprek zoveel mogelijk online via video.4. Aanbieding
Je ontvangt per e-mail een arbeidsvoorwaarden aanbod.5. Nieuwe baan
Je ondertekent je contract digitaal. Welkom bij PostNL!
Senior IT System Engineer
Stichting Centre for Human Drug Research (CHDR)
Leiden, ZHSenior IT Systems Engineer (40 uur per week)
CHDRHet CHDR zoekt een ambitieuze en ervaren Senior IT Systems Engineer (40 uur per week).
Wie zijn wij?
Met een enthousiast en ambitieus team werken we binnen het CHDR (www.chdr.nl) sinds 1987 aan hoogwaardig, klinisch onderzoek naar de effecten van nieuwe en bestaande geneesmiddelen. Het CHDR is gevestigd in Leiden en werkt nauw samen met de Universiteit van Leiden en de klinische afdelingen van het LUMC.
Onze organisatie implementeert de nieuwste technologie en de transitie naar de cloud. Dit heeft grote impact op het IT Team waar we 3 extra posities gaan invullen. Naast de cloud transitie implementeren we ook nieuwe manieren van data acquisitie en analyse (Big Data en Artificial Intelligence). Dit vereist een stabiele en veilige hybride infrastructuur, met implementatie van o.a. SD-WAN. Wij zoeken mensen die hier hun verantwoordelijkheid zien!
Hoe ziet de functie eruit?
Als IT Systems Engineer ben je de technische held die zorgt voor de ontwikkeling, implementatie, en beheer van onze IT systemen. Je bent gedreven, betrouwbaar, leergierig en geïnteresseerd in het werkgebied van CHDR. Dit is een baan met veel variatie en uitdagingen, ideaal als je een volgende stap in je carrière wilt maken.
Je bent verantwoordelijk voor het vinden van solide technische oplossingen en implementaties. Daarnaast zal je deelnemen aan technisch onderzoek en ontwikkeling om voortdurende innovatie binnen het IT landschap mogelijk te maken. Ook zul je fungeren als sparringpartner van methode ontwikkeling en de research staff voor nieuwe applicaties.
Daarnaast zorg je voor (laatste lijns) beheer van het IT landschap en bewaakt de prestaties hiervan. Je bent verantwoordelijk voor een soepele inzet van nieuwe applicaties en update je technische documentatie.
CHDR is een lerende organisatie en wij zorgen voor passende trainingen om jou technische en persoonlijke groei te ondersteunen. De IT afdeling van CHDR bestaat momenteel uit 7 vaste medewerkers en 3 externe medewerkers.
Waar zijn we naar op zoek?
Om succesvol te kunnen zijn in deze rol zijn we op zoek naar iemand met:
HBO werk- en denkniveau;
BSc. Informatica, of ander relevante studierichting aangevuld met ICT opleidingen en certificeringen, met name Azure, O365, Windows Remote Desktop, VMware, Veeam, PowerShell;
Minimaal 3 jaar werkervaring als technisch senior systeembeheerder;
Kennis van technieken voor netwerk- en systeembeveiliging;
Ervaring met Microsoft Windows server 2016; Ervaring met O365 / Azure
Ervaring met onderhoud en probleemoplossing on-premise en cloud;
Planning en organisatie van vaardigheden voor eigen werk;
Ervaring met ITIL;
Servicegerichte mentaliteit;
Samenwerking en overtuiging;
Vermogen en bereidheid om te leren;
Goede beheersing van de Nederlandse en Engelse taal;
Wat bieden wij?
Je komt te werken in een enthousiast, informeel team in een dynamisch, snelgroeiende en internationaal georiënteerde organisatie. Naast een marktconform salaris bieden we goede secundaire arbeidsvoorwaarden, zoals een winstuitkering. We hebben uitstekende koffie, er is elke vrijdagmiddag een borrel (wanneer we weer op kantoor werken) en er worden teamuitjes en personeelsfeesten georganiseerd.
Sollicitatie
Herken jij je in het profiel en spreekt CHDR jou aan? Solliciteer dan voor via de sollicitatie button of stuur je CV en motivatiebrief naar pz@chdr.nl.
Associate Scientist Cell Culture
CLS Services B.V.
Leiden, ZHKeywords
- Cell culture specialist
- Troubleshooting
- GMP
- Process optimisation
- Accurate
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Profile
Are you looking for a challenging role in a pharmaceutical environment? Are you the cell culture specialist who can professionalize this team and do you like trouble shooting? Then we are looking for you!
Based on formation plan and the needs within the QCD Labs organization, we are looking for a motivated and experienced Associate Scientist to strengthen their cell culture team. You will be the cell culture specialist in the team and comfortable enough to be the coach and to train your colleagues on content level.
Main responsibilities:
- Ensure that a high level of quality is maintained in the department;
- Perform cell-based assays (control cell & growth promotion testing);
- Culture cells (e.g. A549, HEK293), to keep cells maintained for assays and projects;
- Act as lead in quality investigations;
- Identify gaps and opportunities for improvement within the department;
- Accurate completion of documentation such as assay run sheets (ARS), laboratory notebooks and logbooks;
- Actively participate in setting up documentation to ensure compliance.
Who we're looking for
For this role we are looking for B.Sc. or M.Sc. candidates with a background in Molecular Biology, Biochemistry, Biophysics and/or protein chemistry. You have a proven track record of at least 5-10 years of (mammalian) cell culture experience, experience with A549 and HEK293 cells is highly advantageous. Additionally, you have experience with prevention and resolving contamination of cell cultures. We are looking for someone with at least 2 years of experience with lab activities in a GMP environment. Experience with quality and laboratory systems such as TrackWise, DMS and eLIMS is considered as a pre. Additionally, you are comfortable with routine activities.
As a person, you are sociable, accurate, pro-active, a teammate and careful.
Company profile
Janssen Vaccines & Prevention B.V. is part of Johnson & Johnson, one of the biggest and most respected health care companies in the world. They are dedicated to bringing meaningful innovation to global health. Their teams focus on the discovery, development, manufacturing, and marketing of novel vaccines to prevent some of the most devastating and complex infectious diseases. These range from respiratory infections like respiratory syncytial virus (RSV) to human immunodeficiency virus (HIV) and pathogens of global concern, such as Ebola and COVID-19.
In this organization, entrepreneurial people are working in a dynamic culture in which innovation and a 'can do' state of mind are of crucial importance. They are continuously looking for enthusiastic, talented people who have the ambition to develop themselves and can be of value to Janssen. The offices of Janssen Vaccines & Prevention are located in Leiden, The Netherlands.
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Department
The QCD labs group is part of the Analytical Development Department of the Pharmaceutical and Analytical Development sector. Overall, it consists of 6 sub-teams (Raw-Materials, Sample Management, Cell Culture, Microbiology, Coordination and Technicians) and is responsible for release and stability testing as well as the corresponding reporting of Janssen’s virus and antibody products for use in clinical trials and the analytical support of the pilot plant activities.
The QCD Labs group focuses on supporting production and laboratory activities with:
- Inspection, release and change management of incoming production raw materials and laboratory chemicals (Raw-Materials Team);
- Sample and Material receipt, handling, storage and forwarding (Sample Management Team);
- Cell Culture services where cells are maintained used for assays and production cell line quality is supported (Cell Culture Team);
- Microbiology group mainly responsible for maintaining controlled state of production clean room and production utilities by environmental and utility monitoring programs (Microbiology Team);
- Coordination of Release and Stability testing and Outsourcing Coordination (Coordination Team);
- Lab technicians’ team is responsible for all internal release and stability testing (Technicians).
Additional vacancy information
| Reference | : | A2100042 | |
| Contract | : | Temporary contract with CLS Services | |
| Education | : | WO/MSc. HBO/BSc. | |
| Employment terms | : | Salary: EURO 45.000 - 55.000 Days of leave: 25 + 11 See here our other employment terms for this vacancy | |
| Publication date | : | 1-3-2021 | |
| Location | : | View location with Google Maps | |
| Contactperson | : | Claudia Erwich-Faaij | |
| +31 (0)31 (0)88 22 77 555 |
Apply
Please apply online here for this job (Job Ref: A2100042). You can also check our other vacancies. You can also follow us on Twitter.
Scientist Immunology/Bacteriology
CLS Services B.V.
Leiden, ZHKeywords
- PhD
- Immunogenicity testing
- Bacterial vaccines
- Assay development
- Certified to work with animal models
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Profile
Within the Bacterial Vaccine department, the Immunology group evaluates the immunogenicity and efficacy of potential vaccine candidates against several bacterial diseases in animal models. Assays to examine humoral and cellular immune responses will be developed and used to generate appropriate scientific data to show proof of concept and thereby enabling vaccine candidates to progress towards clinical phase evaluation.
We are looking for a motivated scientist, who loves challenges, to evaluate the immunogenicity and efficacy of potential vaccine candidates. The role requires knowledge of immunological techniques such as ELISA, killing assays, Electrochemiluminescence assays (ECL), B- and T-cell ELISPOT, proliferation assays, cytokine release assays, intracellular cytokine staining, FACS analysis and cell culturing. You will be responsible for the development and implementation of new assays to measure immune responses of various bacterial vaccine candidates. In addition, it is important to have experience with designing and evaluation of pre-clinical in vivo models. You will work in close collaboration with other scientists and technicians in evaluating vaccine candidates. Also some supervision of the work of technicians is anticipated.
Who we're looking for
For this role we are looking for candidates with a Ph.D in biological/medical sciences with a strong immunology/bacteriology background. You are certified to perform Animal experiments (art. 9 or comparable) and you have experience with developing immunological assays like ELISA, FACS and other assays.
You will actively contribute to the discovery and development of bacterial vaccines therefore we are looking for a flexible, motivated team-player with problem solving capabilities. You maintain accurate written records, and organize your data efficiently (e.g. databases).
Company profile
Janssen Vaccines & Prevention B.V. is part of Johnson & Johnson, one of the biggest and most respected health care companies in the world. They are dedicated to bringing meaningful innovation to global health. Their teams focus on the discovery, development, manufacturing, and marketing of novel vaccines to prevent some of the most devastating and complex infectious diseases. These range from respiratory infections like respiratory syncytial virus (RSV) to human immunodeficiency virus (HIV) and pathogens of global concern, such as Ebola and COVID-19.
In this organization, entrepreneurial people are working in a dynamic culture in which innovation and a 'can do' state of mind are of crucial importance. They are continuously looking for enthusiastic, talented people who have the ambition to develop themselves and can be of value to Janssen. The offices of Janssen Vaccines & Prevention are located in Leiden, The Netherlands.
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Department
The Bacterial Vaccine department (BacVac) at Janssen Vaccines & Prevention is working on the discovery and early development of novel vaccines for bacterial infectious diseases. This working process includes ‘state of the art’ vaccine discovery, with subsequent in vivo evaluation of vaccine candidates in animal models for immunogenicity and/or efficacy. In addition, manufacturing processes are established and optimized, and the resulting clinical trial material is evaluated in human clinical studies.
Additional vacancy information
| Reference | : | A2100030 | |
| Contract | : | Temporary contract with CLS Services | |
| Education | : | PhD. | |
| Employment terms | : | Contract for at least one year Salary: > 4200 Days of leave: 25 + 11 See here our other employment terms for this vacancy | |
| Publication date | : | 12-2-2021 | |
| Location | : | View location with Google Maps | |
| Contactperson | : | Claudia Erwich-Faaij | |
| +31 (0)31 (0)88 22 77 555 |
Apply
Please apply online here for this job (Job Ref: A2100030). You can also check our other vacancies. You can also follow us on Twitter.
Quality Systems Document Control Associate
CLS Services B.V.
Leiden, ZHKeywords
- Quality Documents
- SOP's
- Excel experience
- Independant worker
- Contact with customers
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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.
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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.
(Senior) Manufacturing Fill & Finish Process specialist
CLS Services B.V.
Leiden, ZHKeywords
- GMP
- Manufacturing
- Vaccine/large molecule
- Person in Plant (PiP)
- Outsourcing
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Profile
The Fill & Finish Process (FFP) team is responsible for the external manufacturing of drug product. As manufacturing FFP specialist, you will operate at the technical interface between the Janssen project team and the external drug product manufacturing sites.
Your main responsibilities will be:
- Proper and timely execution of drug product manufacturing activities:
- review of the (master and executed) batch documentation prepared by the manufacturing site and bringing it to the required quality level;
- being physically present during drug product manufacturing (Person in Plant, PiP), resolving issues on the spot and guiding corrective measures if required;
- Establishing and maintaining a trustful and professional relationship with the external drug product manufacturing sites;
- Participating in the multidisciplinary project teams, ensuring alignment with project needs;
- Identifying and implementing improvements in the way of working;
- Being an all-round expert in quality, regulatory, technical and business aspects of external manufacturing.
Who we're looking for
The ideal candidate has a B.Sc. or M.Sc. in pharmaceutical sciences or other relevant disciplines (i.e., pharmacy, (bio)chemistry) with at least 5 years of experience (10 years for senior position) in vaccine and/or large molecule GMP drug product manufacturing. Experience with process development, project management and outsourcing is highly advantageous.
We are looking for a person who is pro-active, flexible and full of initiative. Their highly dynamic environment requires you to have a strong work ethic, expect change and be creative. This position may require travelling and staying abroad for up to 1 week and work independently on location (when possible).
Company profile
Janssen Vaccines & Prevention B.V. is part of Johnson & Johnson, one of the biggest and most respected health care companies in the world. They are dedicated to bringing meaningful innovation to global health. Their teams focus on the discovery, development, manufacturing, and marketing of novel vaccines to prevent some of the most devastating and complex infectious diseases. These range from respiratory infections like respiratory syncytial virus (RSV) to human immunodeficiency virus (HIV) and pathogens of global concern, such as Ebola and COVID-19.
In this organisation, entrepreneurial people are working in a dynamic culture in which innovation and a 'can do' state of mind are of crucial importance. They are continuously looking for enthusiastic, talented people who have the ambition to develop themselves and can be of value to Janssen. The offices of Janssen Vaccines & Prevention are located in Leiden, The Netherlands.
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Additional vacancy information
| Reference | : | A2100021 | |
| Contract | : | Temporary contract with CLS Services | |
| Education | : | WO/MSc. HBO/BSc. | |
| Employment terms | : | Project for at least 1 year. Salary: >3520 Days of leave: 25 + 11 See here our other employment terms for this vacancy | |
| Publication date | : | 5-2-2021 | |
| Location | : | View location with Google Maps | |
| Contactperson | : | Claudia Erwich-Faaij | |
| +31 (0)31 (0)88 22 77 555 |
Apply
Please apply online here for this job (Job Ref: A2100021). You can also check our other vacancies. You can also follow us on Twitter.
Senior Supply Chain Planner (GMP, pharma)
Oxford Global Resources
Leiden, ZH
Are you an expert in inventory / supply chain management in a pharmaceutical or biotechnology setting? Are you looking for a position where you play a key role in managing the supply chain for raw materials for a clinical environment in a large pharmaceutical company? Then we are looking for you!
Job Description
We are looking for an enthusiastic Senior supply chain planner to join the global material planning team. The global material planning team is responsible for the replenishment of raw materials to produce biopharmaceutical products. The Senior supply chain planner is responsible for coordination and execution of all activities related to the planning and procurement of raw materials and components, converting the output of the production schedule into material requirements to ensure availability of the right quantity of components to the production lines when needed.
Responsibilities
- Maintain raw materials / components inventories, while minimizing excess and expired materials.
- Ensure efficient and effective procurement & inventory practices and optimize the balance between quality, service, reliability, and cost.
- Ensure that all material delivery schedules are communicated to the suppliers on time to meet plan requirements.
- Partner with Global Procurement to drive Supplier performance improvement including quality and timely delivery.
- Track and report site / platform level supplier service performance, communicating the information to the relevant parties.
- Collaborate with Quality and Warehouse staff regarding rejected / defective materials, making the physical arrangements with the supplier to ensure a timely return of goods or disposal.
Requirements
- Minimum a BSc degree in life science or in supply chain management
- At least 5 years of experience in a similar environment (Planning, Logistics, or Manufacturing)
- Experienced SAP user
- Experience in the LEAN methodology (preferably in possession of a green or yellow belt)
- Customer focused ensuring that customer requirements are clearly planned for and communicated within the organization
- Results driven, while ensuring the optimization and efficient use of Janssen resources
- Collaborative and cross-functional with all other departments within the company
Benefits
- Contract: 1 year via Oxford, realistic long- term perspective
- Salary: €3600- €4000 gross monthly based on a full-time position
- Holidays: 25
- Working hours: full-time, 32h is possible but not preferred
- Vacancy number: 17144
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!
Project: Scientist Analytical Development (100% remote within EMEA)
Oxford Global Resources
Leiden, ZH
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.
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Type functie
Fulltime
Geplaatst op
5 dagen geleden
Beschrijving
Operational Coordinator International Transport (ENG).
- Leidschendam
- HBO/WO
- Logistiek
- Professional
Wat ga je doen?
As Operational Coordinator International Transport you are responsible for the coordination of all road transport in Europe, including: order management, purchasing, operation, performance management, relationship management and Back Office. You are the first point of contact for our internal & external clients in need of road transportation (FTL/LTL) within Europe. Therefore you collaborate with a selected network of transport partners which are commissioned by our department to fulfil these needs. You also monitor this process regarding both quality and cost and are responsible for the correct administrative handling in our systems. Your most important tasks are: purchase, coordinate with stakeholders and transport partners and organize the implementation of these services. Your most important KPI’s are: cost and performance.
At the Operational Partnerships & Linehaul department we are a team of 16 driven professionals. You work closely together with two other Operational Coordinators International Transport and the Senior Coordinator International Transport. We are part of Cross Border Solutions (CBS), the business unit that provides tailor-made delivery solutions to businesses worldwide under the Spring brand. We deliver special moments to everyone and everywhere.
Onze ambitie
We want to be the preferred logistics solutions provider by delivering special moments every day. Our employees and customers are key. We are always looking for ways to be better. As a result, we need you to act as specialist to your stakeholders regarding road transport requests and issues related to this service. We are looking for someone that knows how to help us increase our performance levels through the optimization of both process and data.
Wat breng jij mee?
- MBO+ or HBO (bachelor) diploma in Logistics or Transportation and at least 3-5 years related work experience in international logistics or e-commerce.
- Good understanding of Cross Border business processes and IT solutions.
- Demonstrated experience with Excel, Power BI and data analysis.
- Excellent English and Dutch written and verbal communication skills. Knowledge of another European language is highly desirable.
You have a no-nonsense mentality and a practical approach. You are an excellent problem solver with a proactive and results oriented attitude. You are good at relationship management and know how to keep an overview when doing many things at the same time. You don’t get easily stressed or frustrated when confronted with the unexpected. Please note that to qualify you need to have all relevant and valid working entitlements (visa/work permit) and must currently reside in The Netherlands.
Wat bezorgen we jou?
- Gross salary indication between € 2.600 and € 3.900 based on 39,25 hours a week (level 8 of the PostNL Collective Labour Agreement).
- Laptop and smartphone.
- Room for growth and for personal development.
- Work location: The Hague Forepark at the International Mail and E-commerce Center (IMEC).
- For further information on our attractive terms of employment please click here.
We offer you a far-reaching and meaningful job. Your solutions, ideas and smart plans have a direct impact on millions of customers around the world. Including you!. We provide a motivating work environment that allows you to develop professionally. Together we are shaping the future of e-commerce.
Interested?
PostNL wants to be everyone’s favorite logistics company. Therefore everyone is welcome to join us. Where you were born, what you believe in and who you love is irrelevant to us. We care only about your unique talent. Pay close attention to the above requirements and explain clearly in your application, and with specific examples, why you are the right person for this role.
You can apply for this position with your resume and cover letter until March 12, 2021 before 9 a.m. On March 16, 2021 we will advise you on the status of your application. A Certificate of Conduct(VOG) and pre-employment screening are part of the selection process.
The video job interviews are planned for March 23, 2021. If you are not available on this date, please let us know in advance.
Sollicitatieproces
1. Sollicitatie
Bedankt voor je sollicitatie! Je krijgt binnen vijf werkdagen een reactie van onze recruiter.2. Telefonisch contact
Hebben we vragen over je CV of motivatie, dan bellen we je.3. Gesprekken
Afhankelijk van de functie heb je één of meerdere gesprekken met onze recruiter, je toekomstige manager en directe collega’s. In verband met het coronavirus voeren we dit gesprek zoveel mogelijk online via video.4. Aanbieding
Je ontvangt per e-mail een arbeidsvoorwaarden aanbod.5. Nieuwe baan
Je ondertekent je contract digitaal. Welkom bij PostNL!