Information Network Technical Specialist
Emerson
RijswijkJob Description
We have an exciting opportunity for keen specialist prepared to take ownership of the successful delivery and support our Information Network projects across Europe.
The role of the Information Networks Technical Specialist is to use their knowledge related to the field of process automation to define and implement solutions for our clients. Our offering includes wireless networks, cyber security, remote access, backup and disaster recovery, IT architecture, virtualization and hosting of the different systems/solutions and this position will allow you to work across the full project lifecycle to see them delivered to the customer. In addition, it will enable you to contribute to business development as well as process, product and solution improvements.
If you are an experienced professional, eager to tackle our challenge, we encourage you to join our team!
IN THIS ROLE YOU WILL:
- Identify and develop opportunities for the delivery of benefits to clients;
- Ensure a good fit between order content and our product/execution capability by guiding scope definition throughout the sales process and participating in the setting of appropriate pursuit strategies.
- Assess and advise on technical and commercial risk of potential and actual business during the sales and execution phases.
- Help define and implement standard methodologies for project pursuits that will lead to long term sustainability and effective implementation.
- Develop and present strategies and material to support business development.
- Provide technical support to the sales team throughout the sales process, including proposal generation, resource estimation, risk assessment and developing support materials which can be used by front offices.
- Support and lead projects that involve technologies within your field of expertise.
- Participate in and lead client support activities (site surveys, feed studies, problem solving, training etc.)
- Internal knowledge transfer - undertake regular knowledge updates, using workshops where appropriate, to the European Engineering team with respect to their specialist fields.
- Ensure that Companyrsquo;s quality control processes and relevant standards are followed.
- Identify possible improvements to the sales and project execution processes, as well as potential improvements in the Emerson products used.
- Assist in defining and crafting standard solutions to improve efficiency.
- Assist in developing implementation capability for solutions based on the supported technology within the organisation.
- Identify and produce marketing material based on work performed such as quantified business results for projects undertaken.
- Develop and maintain relationships with key third parties (vendors of complementary technologies),
- As required provide analysis of the market for our solutions as a whole with a view to growing the business.
Requirements
- Degree level in an engineering discipline, network and computing, Electronics Control and Instrumentation.
- Minimum 5, preferably 10 years of experience in our (Network architecture, DCS, and field implementation)
- Extensive knowledge on network architectures and administration, core network infrastructure components, wireless technology and fieldbus. Ideally have a Cisco CCNA or higher with a specialisation
- Good knowledge on Information technology (IT), Cyber Security, cloud computing, virtualisation, programming software, operating systems, Active Directory, Patch Management, Backup and Recovery
- Experience on project management, scheduling, engineering, procurement, team coordination and sales support
- Strong experience with direct client contact including managing expectations
- Verbal and written communication skills fluent in English
- Master knowledge of Microsoft office including Visio
- Some knowledge of industrial automation systems desirable but not mandatory
- Willingness to travel in Europe is mandatory as part of this job role. Duration and frequency will be variable, but travel is generally for short periods.
WHO YOU ARE:
You are self-motivated, goals-oriented, customer focused individual, passionate about making an impact and always act with integrity. You are not afraid to question the status quo by proposing creative solutions to problems.
Our Offer to You
By joining Emerson as an Information Networks Technical Specialist, you will be working at the heart of our business. This means that the skills and business insight gained can serve as an invaluable foundation toward developing your career within our global organization. We offer plentiful opportunities for advancement and support this through our formal personal development planning process.
Our on-boarding program uses a blended learning approach to get you up and running as quickly as possible. You benefit from Emerson certified trainers with extensive knowledge of our customers, products and applications.
Our global Women in Stem initiative gives you the opportunity to connect with local peers that share the same interest, to promote the diversity & inclusion and early STEM education and to benefit from professional development to access leadership opportunities. Also, we are committed to maintaining a partnership with the Society of Women Engineers (SWE).
Our inclusive company culture celebrates the unique perspectives, diversity of thoughts, and outstanding innovation that come to life when we actively seek to hire and develop the best, brightest team members from all backgrounds. These unique points of view help cultivate fresh thinking and new ideas, ensuring our continued success into the future.
Emerson, a Fortune 500company with %2418.4 billion in sales, more than 20 Innovation, Solutions &Engineering Centers, and 200 manufacturing locations worldwide, is committed tohelping employees grow and thrive throughout their careers. We are innovators,question-askers and problem-solvers. We don’t settle for good enough or “Thisis the way it’s always been done.” Instead, we push ourselves and strive forthe “never been done before.”
Our Automation Solutionsbusiness enables the greatest use of the world's most valuable resources,ensuring the performance and safety of industries that are the backbone ofdaily life.
Our Commercial &Residential Solutions business helps ensure human comfort and health, protectfood quality and safety, advance energy efficiency and create sustainableinfrastructure.
No calls or agenciesplease.
Senior QA Associate
CLS Services B.V.
Leiden, ZHCLS 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, Janssen Vaccines & Prevention (Leiden, Nederland), we are searching for a Senior QA Associate.
Keywords
Profile
As QA Associate, you will work in a multidisciplinary and dynamic team to oversee the technical and analytical development of our COVID-19 vaccine. Mainly QA oversight on analytical development teams, review of method transfer documentation and issue handling for analytical method transfers to external manufacturing sites and laboratories worldwide.
Key responsibilities:
Who we're looking for
We are looking for a MSc candidate with a background in a relevant discipline, like Pharmacy or Bio-Pharmaceutical Sciences. You have 5+ years of analytical experience in a pharmaceutical setting, preferably in Quality Assurance, Quality Control or Analytical Development. General understanding of analytical method validation is required. As a person you are pro-active, agile, and enjoys working in a team. You have good organizational and communication skills. Creativity, problem-solving capabilities and a can-do mentality are key for this position.
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.
Department
The Quality Assurance department at Janssen Vaccines & Prevention in Leiden is a fast-developing department. Janssen V&P is currently working on a full Vaccine pipeline, including a COVID-19 vaccine developed at our site in Leiden and by external collaborations. The QA team is responsible for overseeing and supporting the quality systems, projects and facilities. The opportunities and responsibility for the Quality Assurance department to shape and deliver the right quality are key for the success of Janssen V&P. The group is forward looking, working on improving processes, being customer focused and supports the need for speed. The team is most successful with employees that are proactive and are willing to take ownership, collaborate and are enthusiastic to work in an innovative and focused environment.
Additional vacancy information
Apply
Please apply online here for this job (Job Ref: A2100016). You can also check our other vacancies. You can also follow us on Twitter.
Keywords
- Quality Assurance.
- Analytical method validation.
 |  |  |
Profile
As QA Associate, you will work in a multidisciplinary and dynamic team to oversee the technical and analytical development of our COVID-19 vaccine. Mainly QA oversight on analytical development teams, review of method transfer documentation and issue handling for analytical method transfers to external manufacturing sites and laboratories worldwide.
Key responsibilities:
- Collaborate with functional project teams in a matrix environment to drive team accountability for quality deliverables;
- Represent Quality on cross-functional Teams and participates in site initiatives and projects;
- Review of analytical and technical documentation and independently manage complex method and product issues;
- Review of analytical method transfer documentation package (transfer plans and reports, gap assessments, deviations);
- Applies scientific and engineering principals for problem solving and advise to the teams;
- Safeguards effective interfaces and dependencies with other programs and compliance with technical standards;
- Challenges the status-quo. Involved in conception of new ideas, leads process improvements and contributes to the ongoing development of new procedures, techniques and departmental guidelines;
- Complies to EHS and GMP-standards and has solid JnJ Credo awareness acting accordingly.
Who we're looking for
We are looking for a MSc candidate with a background in a relevant discipline, like Pharmacy or Bio-Pharmaceutical Sciences. You have 5+ years of analytical experience in a pharmaceutical setting, preferably in Quality Assurance, Quality Control or Analytical Development. General understanding of analytical method validation is required. As a person you are pro-active, agile, and enjoys working in a team. You have good organizational and communication skills. Creativity, problem-solving capabilities and a can-do mentality are key for this position.
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.
 |
Department
The Quality Assurance department at Janssen Vaccines & Prevention in Leiden is a fast-developing department. Janssen V&P is currently working on a full Vaccine pipeline, including a COVID-19 vaccine developed at our site in Leiden and by external collaborations. The QA team is responsible for overseeing and supporting the quality systems, projects and facilities. The opportunities and responsibility for the Quality Assurance department to shape and deliver the right quality are key for the success of Janssen V&P. The group is forward looking, working on improving processes, being customer focused and supports the need for speed. The team is most successful with employees that are proactive and are willing to take ownership, collaborate and are enthusiastic to work in an innovative and focused environment.
Additional vacancy information
| Reference | : | A2100016 | |
| Contract | : | Temporary contract with CLS Services | |
| Education | : | WO/MSc. HBO/BSc. | |
| Employment terms | : | Project for 3 months, 28h per week Salary: >4100 Days of leave: 25 + 11 See here our other employment terms for this vacancy | |
| Publication date | : | 29-1-2021 | |
| 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: A2100016). You can also check our other vacancies. You can also follow us on Twitter.
Technical Integrator
Kelly Services Netherlands
Leiden, ZH
Senior Technical Integrator (Dossier Development and Operations)
The Senior Technical Integrator, Dossier Development, is responsible, with some managerial guidance, for developing the technical eCTD sections to support Regulatory CMC dossier applications. With some managerial guidance, coordinates and provides technical oversight for the generation of the CMC dossier of marketing and clinical trial submissions. Coordinates the timeline, virtual document, and generation of the Quality module. Assumes personal ownership and accountability for business results and solutions, working with some managerial supervision. Represents the department on multi-functional project development teams to support regulatory filings.
Authors/drives, as appropriate, sections of the CMC dossier and evaluates/ensures that final versions comply with regulatory requirements and fulfill regulatory agency expectations with some managerial guidance. The Senior Scientist supports the technical functions in the development of responses to health authority inquiries in support of clinical trials as well as marketing applications with some managerial guidance. Evaluates and ensures the completeness, accuracy, and compliance of data provided for all regulatory submissions with some managerial guidance. Ensures all Quality submissions are completed in a timely manner.
Job Scope/Span of Influence
1. Supports dossier strategy / product development plan creation at a compound level
2. Executes dossier strategy / product development plan with a high level of autonomy
3. Direct responsibility for project budgets
4. May lead dossier authoring activities for late stage projects for regulatory filings with some managerial support
5. Identifies business improvement areas and, under some managerial supervision, drives implementation of improvements
6. Develops process and business improvements within own functional organization, and aligns with other departments as needed
7. With some guidance, interfaces directly with CMC/Tech team members, Regulatory, JSC, external service providers and internal Vaccines customers
8. Interfaces mainly internal functional stakeholders, some external stakeholders
9. Influences or persuades others to accept new ideas, approaches or concepts or gains alignment on divergent issues with some guidance
10. Combines technical expertise with management skills. May manage a consultant
11. Manages limited number of projects with standard, rather than accelerated priority, or with assistance of a Senior staff member, manages complex projects with potentially accelerated priority
12. Challenges status quo and has ability to identify innovative approaches to improve products/processes
13. Scope is primarily incremental innovation, within own dept / team.
14. With guidance, resolves cross-functional issues
15. Appropriately identifies and manages key stakeholders, and escalates when needed to obtain senior management support. With some guidance, takes day-to-day decisions on operational priorities for his/her team, and allocates resources accordingly
16. Works mostly independently on a day to day basis, checks in with supervisor weekly
17. Manages functional or project teams with up to 10 members
Education & Experience
PhD with Post-doc experience with 3+ years relevant experience
OR University degree with 6+ years relevant experience OR Equivalent by experience
to apply: send your cv via the link.
Contactperson: Marc Philip van Ittersum 0654712600
Met betrekking tot deze functie fungeert Kelly Services als officieel werkgever. Wanneer je de beslissing maakt om op deze functie te solliciteren zullen jouw gegevens in overeenstemming met Kelly's Privacy Statement worden verwerkt.
Met oog op de AWGB (Algemene Wet Gelijke Behandeling) verwelkomt Kelly Services sollicitaties van iedere geschikte kandidaat, ongeacht etniciteit, geslacht, beperking, religieuze overtuiging, seksuele geaardheid of leeftijd.
------------------------------
Regarding this role, Kelly Services acts as the official employer. When you decide to apply to this role your personal information will be processed in accordance with Kelly's Privacy Statement
In keeping with the AWGB (Algemene Wet Gelijke Behandeling) Kelly Services welcomes applications from any and all eligible candidates regardless of ethnicity, gender, disability, religion, sexual orientation or age.
Assistant Scientist Biophysics and Process Analytics
CLS Services B.V.
Leiden, ZHCLS 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, Janssen Vaccines & Prevention (Leiden, Nederland), we are searching for an Assistant Scientist Biophysics and Process Analytics.
Keywords
Profile
Are you looking for an exciting job in a multinational company and do you have experience with cell culture and analytical assays? Then we are looking for you!
To reinforce the Biophysics and Process Analytics team, we are looking for an Assistant scientist. You are a motivated candidate who enjoys working in a multidisciplinary team.
Your main tasks and responsibilities will be:
Who we're looking for
For this role, we are looking for BSc. (HBO) candidates with a background in Biochemistry, Biophysics, Protein chemistry or related fields. You have knowledge of techniques like qPCR, ELISA, Biological assays, UPLC, CE, DLS and cell culture experience. Additionally, you have affinity for automation and software. Experience in good documentation and quality systems are preferable.
As a person you are flexible, have a pro-active attitude and likes teamwork and outside the box approaches. You are eager to share both theoretical and experimental knowledge and keen to explore new technologies.
Are you the right candidate we are looking for?
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.
Department
The Biophysics and Process Analytics (BPA) team is a young and dynamic group (34 team members), which is part of Analytical Development (AD), responsible for a range of activities focused on biophysical and analytical vaccine characterization. Our responsibilities include project bridging and transfer from late discovery to development, analytical support for process development, scouting exploration and implementation of novel analytical technologies.
Additional vacancy information
Apply
Please apply online here for this job (Job Ref: A2100027). You can also check our other vacancies. You can also follow us on Twitter.
Keywords
- Cell culture
- Sample analysis
- qPCR, ELISA
- UPLC, DLS
- Data analysis and reporting
 |  |  |
Profile
Are you looking for an exciting job in a multinational company and do you have experience with cell culture and analytical assays? Then we are looking for you!
To reinforce the Biophysics and Process Analytics team, we are looking for an Assistant scientist. You are a motivated candidate who enjoys working in a multidisciplinary team.
Your main tasks and responsibilities will be:
- Sample analysis for internal (& external) stakeholders;
- Executing analytical and (molecular-) biochemical methods;
- Cell culture;
- Data analysis and reporting;
- Responsible for documentation e.g. CofAs and trending reports;
- Further responsibilities include instrument maintenance & troubleshooting;
- Written reporting and oral presentations in various settings.
Who we're looking for
For this role, we are looking for BSc. (HBO) candidates with a background in Biochemistry, Biophysics, Protein chemistry or related fields. You have knowledge of techniques like qPCR, ELISA, Biological assays, UPLC, CE, DLS and cell culture experience. Additionally, you have affinity for automation and software. Experience in good documentation and quality systems are preferable.
As a person you are flexible, have a pro-active attitude and likes teamwork and outside the box approaches. You are eager to share both theoretical and experimental knowledge and keen to explore new technologies.
Are you the right candidate we are looking for?
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.
 |
Department
The Biophysics and Process Analytics (BPA) team is a young and dynamic group (34 team members), which is part of Analytical Development (AD), responsible for a range of activities focused on biophysical and analytical vaccine characterization. Our responsibilities include project bridging and transfer from late discovery to development, analytical support for process development, scouting exploration and implementation of novel analytical technologies.
Additional vacancy information
| Reference | : | A2100027 | |
| Contract | : | Temporary contract with CLS Services | |
| Education | : | HBO/BSc. | |
| Employment terms | : | Contract for at least one year. Salary: >2600 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: A2100027). You can also check our other vacancies. You can also follow us on Twitter.
Scientist Immunology/Bacteriology
CLS Services B.V.
Leiden, ZHCLS 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, Janssen Vaccines & Prevention (Leiden, Nederland), we are searching for a Scientist Immunology/Bacteriology.
Keywords
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.
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
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.
Keywords
- PhD
- Immunogenicity testing
- Bacterial vaccines
- Assay development
- Certified to work with animal models
 |  |  |
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.
 |
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.
(Senior) Manufacturing Fill & Finish Process specialist
CLS Services B.V.
Leiden, ZHCLS 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, Janssen Vaccines & Prevention (Leiden, Nederland), we are searching for a (Senior) Manufacturing Fill & Finish Process specialist.
Keywords
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:
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.
Additional vacancy information
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.
Keywords
- GMP
- Manufacturing
- Vaccine/large molecule
- Person in Plant (PiP)
- Outsourcing
 |  |  |
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.
 |
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.
Validation Engineer - New Equipment
CLS Services B.V.
Leiden, ZHCLS 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, Mentor Medical Systems (Leiden, Nederland), we are searching for a Validation Engineer - New Equipment.
Keywords
Profile
Do you have experience with the validation of new equipment in a pharma or medical devices environment? Then this is a great opportunity for you!
As Validation Engineer - New Equipment your daily job consists of:
Who we're looking for
The ideal candidate has a B.Sc. or M.Sc. in a relevant area with 3 to 6 years of Equipment Validation experience preferably in the field of Medical Devices or Pharmaceutical/Healthcare industry. We are looking for someone who takes ownership, is a fast learner and not afraid of jumping in new things getting the information.
Company profile
A Global Leader in Aesthetic Medicine Founded in 1969, Mentor World-wide LLC is a leading supplier of medical products for the global aesthetic medicine market. The Company develops, manufactures, and markets innovative, science-based products for aesthetics markets around the world. Headquartered in Santa Barbara, California, Mentor has manufacturing and research operations in the United States, Mauritius, and the Netherlands. Mentor has made breast implant devices for more than 20 years. Mentor's breast implants are for use in both breast augmentation and breast reconstruction and are of the highest quality, and made under strict standards of design and testing.
Additional vacancy information
Apply
Please apply online here for this job (Job Ref: A2100025). You can also check our other vacancies. You can also follow us on Twitter.
Keywords
- B.Sc./M.Sc.
- Validation
- Medical Devices
- New equipment
Profile
Do you have experience with the validation of new equipment in a pharma or medical devices environment? Then this is a great opportunity for you!
As Validation Engineer - New Equipment your daily job consists of:
- Being both behind laptop / on the shop floor as well;
- Current process improvements - new processes;
- Writing protocols for validation;
- Connecting with Production and Engineers, part of projects most of time;
- Day to day supporting CAPAS: non-conformances;
- Technical investigation process and equipment;
- Stake holder & relationship management, aligned on ways of working being efficient;
- Focus on patient, risk assessment, work safely and efficient (prioritise).
Who we're looking for
The ideal candidate has a B.Sc. or M.Sc. in a relevant area with 3 to 6 years of Equipment Validation experience preferably in the field of Medical Devices or Pharmaceutical/Healthcare industry. We are looking for someone who takes ownership, is a fast learner and not afraid of jumping in new things getting the information.
Company profile
A Global Leader in Aesthetic Medicine Founded in 1969, Mentor World-wide LLC is a leading supplier of medical products for the global aesthetic medicine market. The Company develops, manufactures, and markets innovative, science-based products for aesthetics markets around the world. Headquartered in Santa Barbara, California, Mentor has manufacturing and research operations in the United States, Mauritius, and the Netherlands. Mentor has made breast implant devices for more than 20 years. Mentor's breast implants are for use in both breast augmentation and breast reconstruction and are of the highest quality, and made under strict standards of design and testing.
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Additional vacancy information
| Reference | : | A2100025 | |
| Contract | : | Temporary contract with CLS Services | |
| Education | : | HBO/BSc. WO/MSc. | |
| Employment terms | : | Project for at least 6 months with intention to extend. Partially onsite, 1 - 2 days per week onsite now rest remote, but after Covid-19 restrictions this role is 100% onsite. Days of leave: 25 + 11 See here our other employment terms for this vacancy | |
| Publication date | : | 11-2-2021 | |
| Location | : | View location with Google Maps | |
| Contactperson | : | René Kemps | |
| +31 (0)31 (0)88 22 77 555 |
Apply
Please apply online here for this job (Job Ref: A2100025). You can also check our other vacancies. You can also follow us on Twitter.
(Sr) Technician USP (mammalian & bacterial cell culture)
Oxford Global Resources
Leiden, ZH
For an innovative research oriented international company we are looking for skilled professionals with experience with USP (bioreactor) experience, preferably in the context of vaccine development.
Job Description
Within this company we are looking for experienced technicians with a background in USP. You will work in a multidisciplinary and dynamic R&D environment on various projects such as Corona Vaccine, Polio vaccine, etc. You will work with state-of the art mammalian & bacterial cell culture platforms ranging from shake flasks and roller bottles up to cell factories, suspension formats and fixed-bed bioreactors. under BSLII and BSLIII conditions.You will work hands-on in close collaboration with the DSP and assays departments and play a significant role in tech transfer.
Responsibilities
- Perform hands-on USP experiments ;
- Manage and perform your own research, including reporting and presenting data within your research team;
- Upstream process development (mammalian and microbial cell platforms), scale up in bioreactors and clinical manufacturing;
- You will get acquainted with new equipment and techniques and will also be responsible for writing SOP's, protocols and tech transfer;
- On a regular basis, you will present your results within the USP department;
- You will support and execute general maintenance lab tasks;
Requirements
- BSc (HLO), MSc or PdEng degree in biotechnology, LST, or similar;
- Industrial experience in a GxP and BSL II or III conditions environment is a must have;
- Experience with: Bacterial cell culture, Mammalian cell culture, USP, process development, cell factories;
- Fluency in English, Dutch considered a plus;
- You work well with tight deadlines, can multitask like no other, and can function well both in a team player and independently;
- A flexible and project oriented mindset;
Benefits
- Contract: start with a contract for one year, directly at the company, with outlook on a permanent position;
- Salary: €2500 - €3600 gross per month based on education/ experience;
- Holidays: 25;
- Hours: Full time;
- Region: Leiden;
Vacancy number: 16679
Service Technicus W
Kracht Recruitment
Leiden, ZHWe zijn op zoek naar een Service Technicus W die een goede hands-on mentaliteit heeft en enthousiast wordt van uitdagende complexe installaties.
Deze relatie van Kracht is een installateur die werkt voor meerdere grote opdrachtgevers door heel Nederland. Dit installatiebedrijf is actief in het beheer en onderhoud van complexe installaties in de utiliteit. Het bedrijf is een specialist die haar opdrachtgever volledig ontzorgt op het gebied van installatietechniek. Ze hebben ruime kennis van de nieuwste technieken en aanverwante nieuwe ontwikkelingen in de installatietechniek. Het bedrijf zorgt er voor dat elk project zo optimaal mogelijk verloopt waarbij de klant altijd voorop staat. Er heerst binnen dit bedrijf een informele en open cultuur waardoor jouw ideeën altijd serieus bekeken zullen worden en waar jouw stem ook echt bijdraagt. Door de groei die het bedrijf doormaakt zijn zij op zoek naar een nieuwe Service Technicus W.
Functiebeschrijving
In deze rol als Service Technicus werk jij vaak zelfstandig en heb jij kennis van verschillende systemen en gebouwgebonden W-installaties. Deze taken zullen onder andere naar voren komen:
- Bij klanten ben je het aanspreekpunt en lost installatieproblemen en storingen op;
- Het uitvoeren van testen en het in bedrijf stellen;
- Voorkomen en/of oplossen van storingen bij W technische installaties;
- Het informeren en afstemmen met de klant;
- Meedraaien in storingsdiensten.
Functie-eisen
Onze opdrachtgever werkt zeer klantgericht en daarom zoeken zij dan ook een klantgerichte technicus die gespecialiseerd is binnen de werktuigbouwkundige installaties. Verder wordt het volgende van jou verwacht:
- Je beschikt over een diploma in de richting van werktuigbouwkunde en/of installatietechniek;
- Een aantal jaren ervaring in een vergelijkbare functie;
- Je stelt de klant altijd voorop en bent behulpzaam;
- Kan goed omgaan met veranderingen en werkt nauwkeurig;
- Een goede beheersing van de Nederlandse taal en beschikt over een rijbewijs B;
Arbeidsvoorwaarden
Je gaat als Service Technicus W aan de slag bij een leuke opdrachtgever in een rol waar jij veel vrijheid mag ervaren. Je zal beschikking krijgen over jouw eigen werk auto/bus uitgerust met het beste gereedschap en werken aan mooie utilitaire projecten. Verder mag jij de volgende arbeidsvoorwaarden verwachten:
- Een salaris tussen €2.800,- en €3.800,- bruto per maand aan de hand van jouw werkervaring;
- Beschikking over jouw eigen bus/auto met het nieuwste gereedschap;
- Mogelijkheden voor een telefoon en/of laptop van de zaak;
- Een goede pensioenregeling;
- 25 vakantiedagen en 13 adv-dagen;
- Maximale reiskostenvergoeding.
Technical Implementation and Support Consultant
TransFollow BV
Nootdorp, ZHTechnical Implementation and Support Consultant
Nootdorp / Amsterdam • Fulltime
Technical Implementation and Support Consultant
About TransFollow
TransFollow is the standard for the digital consignment note and one of the most innovative developments in the logistic sector at present. TransFollow offers shippers, carriers and receivers more control and visibility over their logistic processes. Any supply chain partner can connect to the TransFollow platform, exchanging data via their own inhouse software solutions. Pick-up and deliveries are signed for digitally and the status of the shipment can be followed.
TransFollow cooperates closely with (inter)national transport and logistics branch organizations. Distributors in the various countries in combination with software solution providers that integrated TransFollow into their software, are important partners and stakeholders.
The Position
The Technical Implementation and Support Consultant (TISC) is part of the TransFollow Implementation and Support Team. He ensures that (potential) distributors such as TMS / WMS / FMS suppliers, of proprietary software systems of the end users of the platform are supported and guided in the efficient integration and connection of their systems at the TransFollow platform.
The TIC maintains contacts with technical specialists at the parties, provides training, checks and supervises the implementations, both initially and at changes, and certifies the implementations.
In addition, the TIC informs the parties about (imminent) changes as a result of TransFollow release management and provides solutions for problems related to links with software and supports the implementation of technical improvements.
In addition, the TIC supports the Regional Sales Representative in giving demonstrations and is, together with the Regional Sales Representative, responsible for retrieving feedback, requirements and wishes from the (local) market, this for the benefit of the Product Owner.
Main Responsibilities
Your main responsibilities are:
Managing 1st and 2nd level support to customers;
Defining prioritization and level of urgency;
Supervising software distributors and end users (both technical and process-based) who want to realize a connection to the platform;
Maintains contacts with technical specialists at software distributors / end users and provides solicited and unsolicited advices on the implementation;
Having extensive knowledge about the API of the platform and maintaining the (technical) documentation of the API and all related manuals, reference documentation and examples;
Providing access to the various pre-production systems to integrators whilst integrating and provides acces to the production systems when they have demonstrated a correct and safe API implementation;
Assessing API implementations for accuracy and safety and informs the relevant sales representatives of the country organizations;
Supporting deployed applications and servers and services hosted in AWS infrastructure;
Communicating with sales representatives regarding integration status and certification, reports business activities and informs in case of improper;
Monitoring integrators when there is suspicion of an improper API implementation;
What is your profile?
You are a team player and a networker
You have a quality and result orientated mindset
You are good at planning and organizing
Bachelor level of working and thinking
Experience (3 years) as a technical consultant, preferably in the transport sector
You have all the technical insights of :
REST API / HTTP / JSON
SQL, Java
Android
Knowledge and experience with AWS domain and Golang, administration and management is an advantage.
Knowledge and experience with a reporting tool is an advantage
English, Dutch (is an advantage) and a second European language is an advantage.
What do we have to offer you?
A salary in line with market standards and good secondary employment conditions
A work environment with many opportunities
A small but very professional development team
A work environment where working hours can be adapted to your private situation.
Do you want to receive more information, please contact Hans Lip at hlip@TransFollow.org .
We look forward to hearing from you!
Please do not make use of this vacancy as an acquisition opportunity.
Geplaatst op
5 dagen geleden
Beschrijving
Job Description
We have an exciting opportunity for keen specialist prepared to take ownership of the successful delivery and support our Information Network projects across Europe.
The role of the Information Networks Technical Specialist is to use their knowledge related to the field of process automation to define and implement solutions for our clients. Our offering includes wireless networks, cyber security, remote access, backup and disaster recovery, IT architecture, virtualization and hosting of the different systems/solutions and this position will allow you to work across the full project lifecycle to see them delivered to the customer. In addition, it will enable you to contribute to business development as well as process, product and solution improvements.
If you are an experienced professional, eager to tackle our challenge, we encourage you to join our team!
IN THIS ROLE YOU WILL:
- Identify and develop opportunities for the delivery of benefits to clients;
- Ensure a good fit between order content and our product/execution capability by guiding scope definition throughout the sales process and participating in the setting of appropriate pursuit strategies.
- Assess and advise on technical and commercial risk of potential and actual business during the sales and execution phases.
- Help define and implement standard methodologies for project pursuits that will lead to long term sustainability and effective implementation.
- Develop and present strategies and material to support business development.
- Provide technical support to the sales team throughout the sales process, including proposal generation, resource estimation, risk assessment and developing support materials which can be used by front offices.
- Support and lead projects that involve technologies within your field of expertise.
- Participate in and lead client support activities (site surveys, feed studies, problem solving, training etc.)
- Internal knowledge transfer - undertake regular knowledge updates, using workshops where appropriate, to the European Engineering team with respect to their specialist fields.
- Ensure that Companyrsquo;s quality control processes and relevant standards are followed.
- Identify possible improvements to the sales and project execution processes, as well as potential improvements in the Emerson products used.
- Assist in defining and crafting standard solutions to improve efficiency.
- Assist in developing implementation capability for solutions based on the supported technology within the organisation.
- Identify and produce marketing material based on work performed such as quantified business results for projects undertaken.
- Develop and maintain relationships with key third parties (vendors of complementary technologies),
- As required provide analysis of the market for our solutions as a whole with a view to growing the business.
Requirements
- Degree level in an engineering discipline, network and computing, Electronics Control and Instrumentation.
- Minimum 5, preferably 10 years of experience in our (Network architecture, DCS, and field implementation)
- Extensive knowledge on network architectures and administration, core network infrastructure components, wireless technology and fieldbus. Ideally have a Cisco CCNA or higher with a specialisation
- Good knowledge on Information technology (IT), Cyber Security, cloud computing, virtualisation, programming software, operating systems, Active Directory, Patch Management, Backup and Recovery
- Experience on project management, scheduling, engineering, procurement, team coordination and sales support
- Strong experience with direct client contact including managing expectations
- Verbal and written communication skills fluent in English
- Master knowledge of Microsoft office including Visio
- Some knowledge of industrial automation systems desirable but not mandatory
- Willingness to travel in Europe is mandatory as part of this job role. Duration and frequency will be variable, but travel is generally for short periods.
WHO YOU ARE:
You are self-motivated, goals-oriented, customer focused individual, passionate about making an impact and always act with integrity. You are not afraid to question the status quo by proposing creative solutions to problems.
Our Offer to You
By joining Emerson as an Information Networks Technical Specialist, you will be working at the heart of our business. This means that the skills and business insight gained can serve as an invaluable foundation toward developing your career within our global organization. We offer plentiful opportunities for advancement and support this through our formal personal development planning process.
Our on-boarding program uses a blended learning approach to get you up and running as quickly as possible. You benefit from Emerson certified trainers with extensive knowledge of our customers, products and applications.
Our global Women in Stem initiative gives you the opportunity to connect with local peers that share the same interest, to promote the diversity & inclusion and early STEM education and to benefit from professional development to access leadership opportunities. Also, we are committed to maintaining a partnership with the Society of Women Engineers (SWE).
Our inclusive company culture celebrates the unique perspectives, diversity of thoughts, and outstanding innovation that come to life when we actively seek to hire and develop the best, brightest team members from all backgrounds. These unique points of view help cultivate fresh thinking and new ideas, ensuring our continued success into the future.
Emerson, a Fortune 500company with %2418.4 billion in sales, more than 20 Innovation, Solutions &Engineering Centers, and 200 manufacturing locations worldwide, is committed tohelping employees grow and thrive throughout their careers. We are innovators,question-askers and problem-solvers. We don’t settle for good enough or “Thisis the way it’s always been done.” Instead, we push ourselves and strive forthe “never been done before.”
Our Automation Solutionsbusiness enables the greatest use of the world's most valuable resources,ensuring the performance and safety of industries that are the backbone ofdaily life.
Our Commercial &Residential Solutions business helps ensure human comfort and health, protectfood quality and safety, advance energy efficiency and create sustainableinfrastructure.
No calls or agenciesplease.
Source: Emerson