Lediga jobb QRIOS Minds AB i Lund

About the position

We are now looking for a Technical writer and Web Design.



About the position:

1. Technical editing of API conceptual documentation, using GIT process

2. Creating website content, such as blog posts, news, guidelines, technical tutorials targeting developers and technical decision makers

3. Re-arranging the web content to improve overall developer experience. This role will also require knowledge in creating enhanced content (illustrations, schemes, guidelines explaining system architectures).

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Main responsibility:

A skilled technical writer, completely fluent in English (in both UK and US English). You should have a deep interest in text creation in different formats.
Edit and transform internal documentation material for external publishing according to brand and writing guidelines.
Create and edit content (texts, images, videos) for pages and sections on the Developer World websites in time for product, tool and service releases and updates.
Create and make sure sustainable information architecture is set up in sync with business needs.
Web-editing experience with basic UX/UI understanding to be able to re-arrange web content to fit the needs of the target audience.
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Requirement for this position:

Experienced in working with technical content creation and editing it for an external target group.
Experienced in working with branding and writing guidelines.
Knowledge of managing online technical documentation through its lifecycle.
Familiarity with WordPress or similar content management systems for online publishing
Prior experience of working with Content Management System (WordPress) to test new editorial features and suggest improvements.
Structured, and focused on both details as well as overall goals.
Comply with company branding and guidelines.
Service minded, flexible, self-directed and with a drive to take responsibility.
A team player that easily adapts and drives improvements in a positive way.
Eager to deliver the best quality experiences possible.
Social and positive.
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Good to have:

Familiarity with a markup language, which could be Markdown, AsciiDoc, HTML, SGML, XML, or similar.
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About the organisation
At QRIOS we have curious experts in IT, Life Science, Engineering and Management.
We are a consultancy company that is strongly inspired by those who never stop looking for new solutions.
QRIOS MINDS GO FURTHER. Are you curious about QRIOS? Dont hesitate to get in touch and will tell you more about our work and offerings. Curious people learn more. Stay QRIOS.

We welcome your application already today. Visa mindre

About the position
Do you never stop looking for new solutions? Join QRIOS Life Science & Engineering in the role as a Electrical Engineer.
At QRIOS we have curious experts in Life Science, Engineering, Management and IT.
We are a consultancy company that is strongly inspired by those who never stop looking for new solutions.

Responsibilities
The Electrical Designer will prepare control panel designs for order projects and potential development projects.
Design, develop and maintain electrical control systems and/or components to required specifications, focusing on economy, safety, reliability, quality and sustainability.
*Eplan P8 is mandatory, preferably Pro Panel and routing.
*Familiar with global standards for electrical control panels, especially IEC (EN60204).
*Electrical Engineering education or equivalent experience.
*Fluent in Swedish and English

About the organisation
At QRIOS we have curious experts in Life Science, Engineering, Management and IT.
We are a consultancy company that is strongly inspired by those who never stop looking for new solutions.
QRIOS MINDS GO FURTHER. Are you curious about QRIOS? Dont hesitate to get in touch and will tell you more about our work and offerings. Curious people learn more. Stay QRIOS.

We welcome your application already today. Visa mindre

Adapteo är marknadsledande och den största leverantören i norra Europa av anpassningsbara byggnader i form av modulhus. Våra moduler används vanligtvis för kontor, skola, förskola och boende. Våra kunder finns inom offentlig sektor och industrin i Sverige. Som Projektkoordinator hos Adapteo blir du en del i denna snabbrörliga värld med intressanta projekt för förskolor, skolor, kontor, vård och boende.

Vill du ha ett omväxlande arbete med många kontaktytor? Då kan detta vara något för dig!Rollen innebär kommunikation och koordinering i ett engagerat team bestående av säljare, projektutvecklare och projektledare.

 Arbetsuppgifter
I dina arbetsuppgifter ingår att genomföra enklare ritningar i CAD. Du kommer att hantera projektdokumentation såsom hyresavtal och ritningar och uppdatera kunddatabaser. Fakturering och uppdatera ekonomiska uppgifter för hyror ingår i uppgifterna. Du blir kontorsansvarig, vilket innebär att stötta teamet med telefon/kontorsservice, ansvara för att planera möten och att uppdatera måldokumentet månadsvis för säljkontoret.

Kvalifikationer
Vi söker dig med erfarenhet från en liknande roll. Du trivs med att arbeta serviceinriktat och flexibelt. Du arbetar strukturerat och är mån om ordning och reda. Du har erfarenhet av att arbeta i affärssystem och kan grunderna i Excel. Utbildning från Ekonomiskt gymnasium är en fördel.

Vi erbjuderDu får en viktig roll i ett företag med en stark laganda och bra samarbete i hela organisationen. Du ingår i ett nätverk med fem koordinatorer i Sverige som träffas regelbundet.

Om företaget
Adapteo är den ledande partnern inom anpassningsbara byggnader i norra Europa. Vi bygger, utvecklar, hyr ut och säljer anpassningsbara lokaler för förskolor, skolor, kontor, vård och boende. Med Adapteos cirkulära byggnadslösningar kan kunderna transformera, skala upp, skala ner och återanvända, allt eftersom behoven förändras. Det är så vi bygger anpassningsbara och hållbara samhällen. Adapteo AB har försäljningskontor i Stockholm, Göteborg, Västerås, Umeå och Lund samt lager- och underhållsverksamhet i Enköping och Jönköping. Vi är ett 80-tal anställda runt om i Sverige som är engagerade och arbetar tillsammans för att nå våra mål. Vi har en bra sammanhållning och drivs av att göra det lilla extra för Adapteo.

Varm välkommen med din ansökan! Visa mindre

I am searching for a scientist who can work independently and has experience working in the medtech/ pharma industry.
We have a customer within med-tech industry in Lund, who is searching for a consultant that will join the water systems team for 1 year.

Responsibilities
Pure water is essential for treatment of dialysis patients, and we are right now looking for a consultant that can join our water systems team. Our water systems team in Lund manages an existing product on the market. The team is right now kept busy with compliance work. Additionally, we are managing continuous development and improvement of the platform as well as addressing supply chain challenges by qualifying new suppliers and components.

The person shall be able to work independently, take responsibility, deliver results with self-confidence and drive the tasks/studies to end goal. Primary tasks and responsibilities will vary over the assignment but will most likely include:

• Change owner in Trackwise for changes related to our water systems
• Conduct design reviews
• Work package lead (having a lead role for certain activities within the team)
• Develop design control documentation
• Defect management in HP ALM
• Develop test documentation (protocols and reports)
• Test planning and coordination

Your profile
• Bachelor or master’s degree in Biomedical engineering, Mathematics, Engineering, Computer Science, Chemistry or Bioinformatics OR equivalent through experience
• Experience from medical device and/or drug development is an advantage
• Good Document Practices
• Strong analytical and problem-solving skills
• Must be able to work on multiple simultaneous tasks with limited supervision
• Quick learner, motivated self-starter
• Structured / Organized
• Excellent communication and team collaboration skills

About the organisation
This is a consultant assignment at our customer in Lund for 1 year. During the assignment you will be hired by us at QRIOS Life Science & Engineering.

QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you. Being a consultant at QRIOS gives you opportunities to try different industries, companies and roles. Visa mindre

About the position
Here is the opportunity to take on a specialist role in Powder Technologies at Bonesupport.

You will with your drive and competence, contribute to improving the current CERAMENT products and developing modified and new bone graft substitutes, in a company where the passion for the products is noticeable.

As the specialist in Powder Technologies, you will drive improvements and development related to powders, both internally and externally. You will provide scientific knowledge on powder characteristics and be the subject matter expert, participate in problem solving and scaling up to production.

Responsibilities
• Driving projects, which concern the ceramic powder part of Bonesupport’s products
• Strengthen product research and development
• Explore advanced material and powder characterization methods and analytical techniques, for deeper understanding and concrete application
• Plan, perform and report investigations, verifications, and validations
• Transfer knowledge and collaborate with both internal and external parties

Your profile
Must have:
• Ph.D. in inorganic Chemistry, Chemical Engineering with focus on Ceramic Powder Technology or Material Science, and a minimum of 2 years work experience from the industry OR
• M.Sc. in inorganic Chemistry or Chemical engineering in the above and 5+ years of work experience from the industry
• Experience in advanced material characterization methods and analytical techniques such as ICP, FTIR, BET, XRD, SEM, Raman spectrometry and LC-MS
• Knowledge in surface chemistry, dissolution, precipitation, trace elements, foreign phase content, crystallinity, elemental impurities, specific surface area and particle size distribution
• Experience in powder processing methods
• Experience in project management
• English at a professional level

Nice to have:
• Experience in transferring research and processes from lab to production
• Experience from medical device or pharma industry
• Experience in bone graft substitutes
• Understanding of ISO 13485 and documentation requirements according to design control processes
• Experience in working according to international pharmacopoeia

At Bonesupport we value personal skills as much as professional qualifications, and in this role, personal competences are crucial for success. To succeed in the role, we see that you bring the followings:
• You have excellent communication skills
• You are a motivated self-starter who takes initiatives and drives projects independently
• You are result oriented and feel comfortable delivering according to sharp deadlines
• You are analytical and prioritize quality

About the organisation
At Bonesupport you will be working together with skilled, dedicated people who enjoy working in a fast growing and innovative organization. We offer a dynamic and stimulating workplace and strive for generating great teamwork, innovation, passion, and performance. We believe in our journey and take pride in what we do!

BONESUPPORT (Nasdaq Stockholm: BONEX) develops and commercializes innovative injectable bio-ceramic bone graft substitutes that remodel to the patient’s own bone and have the capability of eluting drugs. BONESUPPORT’s bone graft substitutes are based on the patented technology platform CERAMENT. The company is conducting several clinical studies to further demonstrate the clinical and health economic benefits its products deliver. The company is based in Lund, Sweden, and the net sales amounted to SEK 213 million in 2021. Please visit www.bonesupport.com for more information.
BONESUPPORT and CERAMENT are registered trademarks of BONESUPPORT AB.

QRIOS Life Science & Engineering is supporting BONESUPPORT AB on this recruitment. QRIOS is a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER
We are interviewing candidates continuously and warmly welcome your application today.

#LI-UE1 Visa mindre

About the position
We are looking for a EHS Specialist for our customer in Lund. In this position the right candidate will be responsible for the development and implementation of safety and environmental programs. The candidate will also provide the employees with professional, technical problem solving and administrative coordination of safety and environmental programs, policies and regulations.

The customer is a leading company within med-tech and is located in Lund.

Responsibilities
• Administer and coordinate compliance with all safety, hazardous material, hazardous and non-hazardous waste programs.
• Perform and/or assist in industrial hygiene monitoring for the site to determine employee and environmental safety.
• Provide technical information on safety and environmental issues on new equipment, method of performing work, with equipment, and risk to employee health.
• Conduct or participate in audits for compliance with site programs and policy, reporting the results to the site environmental and safety manager.
• Provide non-routine problem solving to engineering and research and development groups through participation in committees.
• Prepare and/or assist with composing Regulatory & Agency, Corporate, and Divisional reports.
• Review and update all safety and environmental programs and procedures as needed.
• Provide specialized training required by local/regional regulations to employees.

Your profile
Education and/or Experience:
• Bachelor's Degree in Environmental, Safety or related field.
• 3-5 years experience in the EHS field with specific concentration in OSHA and EPA regulations.
• 2-4 years experience in a pharmaceutical manufacturing environment
• Alternately the incumbent must become certified within 1 year of employment.

Qualifications / Skills
• Knowledge of cGMP manufacturing.
• Knowledge of basic laboratory and pharmaceutical production equipment including but not limited to: autoclaves, process tanks, incubators, analytical equipment, and CIP/SIP systems.
• Incumbent must be proficient in a variety of mathematical disciplines
• Must be able to read and follow detailed written instructions and have good verbal/written communication skills.
• Good interpersonal skills and be able to work effectively and efficiently in a team environment.
• Must have the following personal attributes: integrity and trust, work ethic, sound judgment, intellectual honesty, pragmatism, courage and conviction.
• Must have respect for individuals and the diverse contributions of all.

About the organisation
This is an consultant assignment at our customer in Lund for one year with possibility of extension. During this time you will be hired by QRIOS.

QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you. Being a consultant at QRIOS gives you opportunities to try different industries, companies and roles. Visa mindre

About the position
Here is the opportunity to take on an expert role in Powder Technologies at Bonesupport. You will with your high competences, contribute to improve the current CERAMENT products and take part in the development of modified/new bone graft substitutes, in a company where the passion for the products is noticeable.

As the expert in Powder Technologies, you will be involved in the core business products of Bonesupport. You will take part in improvements and development, as the subject matter expert, both internally and externally. You will provide deep scientific knowledge in the understanding of powders and their characteristics. You will be the expert advisory in problem solving related to this area, with the competence to provide insights from research and development, including scaling up to production.

Depending on which strengths you bring, you will also be part of shaping the role going forward.

Responsibilities
• Be responsible in driving research activities/projects, which concern the ceramic (Calcium Sulfate and Calcium Phosphate) part of our products
• Strengthen product research and development together with the existing team
• Act as Project Manager in selected projects and as a project member in other projects
• Plan, perform and report on investigations, verifications, and validations
• Explore advanced material characterization methods and analytical techniques, for deeper understanding and concrete application in the use for product portfolio
• Transfer knowledge

Your profile
Must have:
• Preferably a Ph.D. in inorganic Chemistry or Chemical Engineering in Ceramics, Powder Technology, Material science, Mineralogy and a minimum of 2 years work experience from the industry OR M.Sc. in inorganic Chemistry or Chemical engineering and 5 years + work experience from the industry
• Experience in advanced material characterization methods and analytical techniques, such as: ICP / FTIR / BET / XRD / SEM / Raman spectrometry / LC-MS / ESCA / and AFM
• Knowledge in the areas of colloid and surface chemistry, dissolution, precipitation, trace elements, foreign phase content, crystallinity, elemental impurities, specific surface area and particle size distribution
• Experience in transferring research and/or processes from lab to production
• Experience in powder processing methods
• English written and spoken

Nice to have:
• Experience from medical device or pharma industry
• Experience in project management
• Experience in bone graft substitutes
• Understanding of ISO 13485 and documentation requirements according to design control processes
• Experience in Medical Device Regulations
• A broad international network in relevant areas

At Bonesupport we value personal skills as much as professional qualifications, and in this role, personality is crucial for success. To succeed in the role, we see that you bring the following personal competences:
• Strong collaboration and excellent communication skills
• You are result orientated and feel comfortable to deliver in a high pace environment.
• You are analytical and prioritise quality
• The ability to quickly get involved in new tasks

About the organisation
At Bonesupport you will be working together with skilled, dedicated people who enjoy working in a fast growing and innovative organization. We offer a dynamic and stimulating workplace and strive for generating great teamwork, innovation, passion, and performance. We believe in our journey and take pride in what we do!

BONESUPPORT (Nasdaq Stockholm: BONEX) develops and commercializes innovative injectable bio-ceramic bone graft substitutes that remodel to the patient’s own bone and have the capability of eluting drugs. BONESUPPORT’s bone graft substitutes are based on the patented technology platform CERAMENT. The company is conducting several clinical studies to further demonstrate the clinical and health economic benefits its products deliver. The company is based in Lund, Sweden, and the net sales amounted to SEK 213 million in 2021. Please visit www.bonesupport.com for more information.
BONESUPPORT and CERAMENT are registered trademarks of BONESUPPORT AB.

QRIOS Life Science & Engineering is supporting BONESUPPORT AB on this recruitment. QRIOS is a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER
We are interviewing candidates on a continuous basis and welcome your application today. Visa mindre

Adapteo skapar flexibla byggnader för ett mer modernt, hållbart och tillgängligt samhälle.
Som Projektledare hos oss leder du projekt för förskolor, skolor, kontor, vård och boende. I Distrikt Syd ingår du i ett team på nio engagerade medarbetare. Du får ett omväxlande arbete i en trevlig miljö.

Om tjänsten
Som projektledare ansvarar du i huvudsak för projektets framdrift vad gäller, ekonomi, tidplaner, mål, kommunikation och kvalitet. Dina kontaktytor är många och du blir en viktig nyckelperson som leder samarbetet mellan både kunden, det interna teamet och utvalda underentreprenörer.

Dina arbetsuppgifter i huvudsak
• Planera och genomföra etableringar och avetableringar av projekt. Våra uppdrag omfattar både hyresprojekt och entreprenader med formell slutbesiktning och försäljning till kund.
• Leda och styra UE enligt tidplan och vidta åtgärder för att följa våra riktlinjer samt lagstiftning gällande kvalitet, miljö och arbetsmiljö.
• Ansvara för ekonomin i projektet, dvs fakturering, uppföljning, ÄTA och prognos.
• Inköp och upphandling av UE

Vem är du?
Vi söker dig med relevant byggteknisk utbildning och minst tre års erfarenhet av byggledning. Kunskaper om prognosarbete och inköp är meriterande. För att lyckas i rollen behöver du vara kommunikativ, ha samarbetsförmåga samt vara effektiv och drivande. B-körkort krävs.

Om verksamheten
Adapteo är ett ledande flexibelt fastighetsbolag i Nordeuropa. Vi bygger, hyr ut och säljer anpassningsbara byggnader för skola, förskola, kontor, boende och event. Vårt samhälle står inför stora förändringar under kommande år och oavsett vad för utmaningar framtiden medför anser vi att anpassningsförmåga är den bästa lösningen. Med en modulär och cirkulär byggteknik kan vi förändra, återanvända, skala upp och skala ner våra byggnader på ett par veckor. Våra byggnader kan användas i några dagar eller under obestämd tid, alltid optimerade för aktuella behov. Det är så vi bygger anpassningsbara samhällen.
Adapteo Group är verksamma i Sverige, Finland, Norge, Danmark, Tyskland och Nederländerna. År 2020 uppgick Adapteo Groups omsättning till 231 miljoner euro. Vi är idag ca 500 anställda, och har vårt huvudkontor i Stockholm och Vanda.
Adapteo AB har försäljningskontor i Stockholm, Göteborg, Västerås, Umeå och Lund samt lager- och underhållsverksamhet i Enköping och Jönköping. Vi är ett 70-tal anställda runt om i Sverige som är engagerade och arbetar tillsammans för att nå våra mål. Vi har en bra sammanhållning och drivs av att göra det lilla extra för Adapteo.
Adapteos kärnvärden ligger till grund för vår verksamhet och vår kultur. Som medarbetare, kund eller annan intressent ska mötet med Adapteo genomsyras av att vi är Proaktiva, Samarbetsvilliga och Engagerade.


Varmt välkommen med din ansökan. Urval sker löpande, ansök därför redan idag genom att klicka på ansök på https://www.qrios.se. Visa mindre

Are you up for a challenging assignment being part of a project group creating a new class of cardiac support devices, to improve the care of the growing number of people with heart failure?

QRIOS Life Science and Engineering are now looking for a mechanical engineer within the area of fine mechanics, for our customer, a Swedish innovation-driven company based in Lund.

The assignment is planned to start shortly and will reach until the summer 2022. There is a flexibility to work 50-80%.

About the position
You will be a part of a multidisciplinary project team, consisting of approx. 5 people. Together as a team you will succeed to take this world class product to the next step.
You will be involved in the development process, to complete, finalise and verify the product before it goes into the stage of preclinical trials.
Your contribution to the team will be to support the project group with your fine mechanical skills and knowledge.

You could be working remotely from anywhere in northern Europe for most of the time but need to make yourself available to come onsite in Lund for some weeks, to meet and work together with the dedicated project team.

Your profile
We are looking for a mechanical engineer with hands-on experience from fine mechanics.
It is an advantage if you have experience from the medical technology/device industry, but it is not a must. Most important is that you have hands-on skills and experience from fine mechanics and an understanding of the creation and product development of fine mechanics. What is possible and how?

The purple squirrel also has experience from one or more of the below areas.
- Movable fine mechanics and micromechanics
- Knowledge of implants, preferably minimally invasive
- Knowledge of heart implants
- Knowledge of components made of Nitinol
- Knowledge of components made of Titanium
- Knowledge of 3D-printed micro-details in metal

Fluent written and spoken English is a requirement.

You enjoy working in projects with multi-functional teams involved.
To be successful you are analytical, detail oriented and organized. You have solid communication skills and a flexible mindset and enjoy working in a fast paced, changing and time sensitive environment.

About the organisation
Our customer is an innovative company developing a revolutionary, minimally invasive long-term cardiac support device technology, with the aim to increase patient survival rates, improve the patient’s quality of life and reduce healthcare costs, meeting both clinical and socio-economic needs.

You will have the opportunity to be part of an environment where there is an intense drive, an encouragement of new, innovative ideas, genuine knowledge, and a global thinking, which creates a creative and flexible workplace.

QRIOS Life Science and Engineering is supporting our customer in the search for a consultant to this assignment. During the assignment you will either be employed by QRIOS Life Science and Engineering or work as your own independent consultant.

At QRIOS we have curious experts in IT, Life Science and Engineering. We are a consultancy company that is strongly inspired by those who never stop looking for new solutions. QRIOS MINDS GO FURTHER.

We will interview candidates continuously and welcome your application today. Visa mindre

Do you want to contribute to a top quallity medical research? We are searching for a candidate that wants to work for a global meditech company in Lund that touches the lives of millions of people around the world every day.

Responsibilities
Works as part of a team performing engineering work in Risk Management through application of standard engineering techniques, procedures and criteria.
• Support design teams in risk process execution using relevant methodologies, tools and techniques in the development/maintenance of Risk planning and deliverables.
• Collaborates with cross-functional resources (e.g., hardware, clinical, human factors etc.) involved in Risk Management process activities.
• Acts independently with minimal supervision. Expected to make suggestions on improvements based on recent technical knowledge.
• Manages risk-related Design History File (DHF) elements and associated documents, including the Risk Management File (RMF).
• Present and explain Risk Management File documentation and/or Baxter Product Risk Management procedure during external audits.

Your profile
• Experience with tools related to structured risk control activities, for instance Failure Mode Effects and Analysis (FMEA), Fault Tree Analysis (FTA) with support from SW like DOORS and Windchill Quality Solutions (WQS) and/or other Requirements Management & Risk tools as well as in Excel.
• Strong critical thinking skills.
• Familiarity with regulations and standards related to Risk Management: (e.g. European Medical Device Regulation 2017/745, ISO 13485, ISO 14971, IEC 60812, IEC 61025, IEC 62366, IEC 60601 etc.).
• Requires strong organization- and communication skills, with the ability to interface with both technical and non-technical personnel throughout the organization.
• Able to work with a cross-functional team in a fast-paced environment.
• MSc degree in Engineering required with at least 2-4 years of practical experience, preferably in Medical Devices.

About the organisation
This is a a consultant assignment at a global meditech company in Lund until 2022-12-31. During that period you will be employed by QRIOS Life Science & Engineering.
Submit your application today! If you have any questions regarding the consultant assignment feel free to contact us QRIOS. Visa mindre