Lediga jobb som Forskningschef i Malmö

Job description
If you are passionate about driving impactful research and contributing to the advancement of MedTech innovations, we might have the role for you! We are currently looking for a Senior Clinical Research Associate to join the global Medical & Scientific Affairs team at our Client company, for a temporary maternity cover. Our client is a a global medical device leader dedicated to significantly improving the patients' quality of life, by delivering class II and III medical devices.


This role offers a unique opportunity to engage in the full spectrum of clinical studies, from project inception and planning, study monitoring and reporting of study findings. Moreover, your role extends beyond research, as you'll partner with our commercial teams to translate key findings into impactful messaging for a wide range of audience. You will immerse yourself in every aspect of the process, contributing to both short-term objectives and long-term strategic goals.


This is a consulting assignment within Randstad Life Sciences which is specializing in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.


If you are ready to make a difference and join our customer exciting growth journey, apply before the 30th of December 2025. Selection and interviews will be ongoing. The starting date will be agreed upon by all parties.

Responsibilities
Oversee and manage development of clinical investigation documents
Manage and coordinate ethical and competent authority submissions and approvals.
Communication with investigators and internal stakeholders.
Oversee analysis study data and compile comprehensive reports on study outcomes.
Collaborate closely with commercial teams to integrate study findings into promotional materials
Ensure alignment of SOPs and templates to latest regulations (ISO 14155, MDR, etc)
Train and mentor new team members on clinical investigation processes


Qualifications
We are looking for someone with previous experience and in-depth knowledge of clinical investigation processes, including protocol development, monitoring, ethical review submission, and reporting of study data. You are currently working with clinical studies of medical devices, and are now looking for the opportunity to independently drive study activities.


PhD or Master's degree in Life Science, Natural Science, or Medicine.
Minimum of 3 years' experience in clinical studies within the MedTech industry, and working in accordance with ISO-14155 and MRD
Experience with ethical and competent authority submissions 
Proficiency in English and familiarity with Microsoft Office suite.
Experience with study management tools such as eTMFs and EDCs is highly desirable.


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential. With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Sharkmob is an innovative AAA video game company dedicated to creating engaging multiplayer experiences. Our research lab focuses on understanding what drives players and enhances their enjoyment. We collect insights using traditional research methods, whether through usability testing or playtests, to guide our developers in making data-driven decisions. Our Data, User Research, and Community teams work closely to interpret player behaviors and conduct extended research in collaboration with local universities.
As a Lead User Researcher, you will lead and develop your team. You will alsoalign user research activities across multiple projects, driving player-centric game development.
Key Responsibilities Actively share knowledge and maintain key stakeholder relationships.
Develop, promote, and ensure good user research practices.
Design studies using experimental design and research methodology.
Ensure User Researchers have the necessary tools and resources.
Execute tests, analyses, reports, and presentations.
Guide game teams in planning user research strategies for the lifecycle of their games.
Promote collaboration between Data, UX, Community, and Marketing teams.
Provide consultative support and guidance to senior stakeholders.
Recruit, lead, and develop User Researchers at all levels.
Support development teams in taking a user-centered, evidence-based approach to research.


Being a Lead at SharkmobAs a Lead, we expect you to support team members by providing the resources, leadership, and tools they need to be successful.You facilitate collaboration, teamwork, and champion your team's achievements and successes. By embodying these principles, you as a leader can help develop a culture of creativity, collaboration, and continuous improvement that benefits not just those you lead but also those around you, as well as Sharkmob as a studio.
We expect you to lead by example - to inspire and motivate others. You champion the studio and act as a first point of contact for your direct reports. You stand behind your team, take decisions and act in accordance with the values of Sharkmob.
Your Experience & Requirements 10+ years of experience in user research or usability testing.
Bachelor's degree or higher in experimental/social/cognitive psychology, human-computer interaction, or equivalent industry experience.
Excellent written and verbal communication skills.
Extensive experience with user interviews, surveys, moderating research sessions, and usability tests.
Passion for video games is beneficial, and experience in game development or the entertainment industry is desirable.
Strong analytical skills with a background or coursework in descriptive and inferential statistics.


Who we areSharkmob was founded in 2017 and has offices in Malmö, Sweden, and London, UK. The studio develops AAA-quality games for PC and console, using the Unreal Engine to power its ambitions of taking multiplayer games to new heights.
Currently, we are working on two major projects: Exoborne – a Sharkmob original game created in Malmö, is a tactical, open-world extraction shooter set in a United States torn apart by apocalyptic forces of nature. The second project, developed in London, is another Sharkmob original IP yet to be announced. Our first game, Bloodhunt - a battle royale set in the Vampire: The Masquerade universe, was released on 27 April 2022.
At Sharkmob, we are committed to building an inclusive team that represents diverse backgrounds, perspectives, and skillsets – because we believe that helps us create great games. We welcome all candidates who are aligned with our core values of shared ownership, creating great games, and, last but not least – having fun! We hope you want to join us on our adventure and become a part of our crew. You can find more great perks of being a crew member. If you want to know more about Sharkmob and our projects, visit our homepage. Visa mindre

As the Manager for User Insights, you will centralize the understanding of our gaming community, ensuring that our products and strategies align with user needs, sentiments, and behaviours. Acting as the bridge between user research, in-game analytics, market trends, and company/product strategy, this position has a critical impact on product development, marketing, and competitive positioning.
Central to the Manager's mission is building, scaling, and refining our current user research and data teams while also exploring the future potential of a market research team. Recognizing each unit's unique strengths and challenges, the Manager will be pivotal in ensuring these teams are well-resourced, strategically aligned, and operate at the forefront of industry best practices.
One of the Manager's key challenges will be ensuring the seamless integration of user insights into our development teams' daily operations. The Manager will ensure insights are translated into actionable development directives by championing close collaboration, fostering open communication channels, and facilitating regular feedback loops.

ResponsibilitiesLeadership & Strategy
Lead, mentor, and grow the User Research and Data teams.
Plan for the potential integration and leadership of a future Market Research team.
Set strategic goals for the Insights department in alignment with company and project objectives.
Champion a data-informed culture, ensuring insights and research are at the forefront of decision-making processes.

User Research
Oversee user research initiatives, from usability studies to in-depth interviews, ensuring actionable and relevant insights.
Promote the integration of user feedback into product development and design processes.
Advocate for the user, ensuring their needs and behaviors are well understood and addressed.

Data Analysis & Management
Guide the Data team in extracting, analyzing, and presenting data from various sources.
Ensure the integration of quantitative data with qualitative findings for a holistic understanding of user behaviour and preferences.
Oversee the development and maintenance of data infrastructures, ensuring robustness, scalability, and compliance with data privacy regulations.

Data Maturity & Integration
Drive the growth of data maturity, championing the consistent and meaningful use of data in all facets of our operations.
Develop and oversee comprehensive training and education initiatives to empower teams with data literacy and analytical capabilities.
Engage with stakeholders at all levels to garner buy-in, ensuring that insights are fully integrated into our game development processes and strategies.

Collaboration & Communication
Act as the primary liaison between the Insights department and other teams, ensuring effective communication and collaboration.
Present insights and findings to stakeholders, ranging from developers to senior management.
Foster cross-functional relationships to facilitate the effective implementation of recommendations from research and data analytics.

Continuous Improvement
Stay updated with the latest methodologies, tools, and trends in user research and data analytics.
Drive innovation in research methods and data interpretation.
Establish and maintain best practices and standards for the Insights department.
Requirements Bachelor’s degree in a related field (e.g., psychology, sociology, statistics, data science, market research). Advanced degree preferred.
5+ years of experience in user research, data analysis, or a related field, with at least 2 years in a managerial role.
Strong leadership and people management skills.
Excellent communication and presentation skills.
Proficiency in qualitative and quantitative research methodologies.
Experience with data analysis tools (e.g., , Python, R) and research tools (e.g., usability testing software, survey platforms).
Ability to synthesize complex data into clear, actionable insights.
Strong organizational and project management skills.
Who we are
Sharkmob was founded in 2017 and has offices in Malmö, Sweden, and London, UK. The studio develops AAA-quality games for PC and console, using the Unreal Engine to power its ambitions of taking multiplayer games to new heights.
Currently, we are working on two major projects: Exoborne – a Sharkmob original game created in Malmö, is a tactical, open-world extraction shooter set in a United States torn apart by apocalyptic forces of nature. The second project, developed in London, is another Sharkmob original IP yet to be announced. Our first game, Bloodhunt - a battle royale set in the Vampire: The Masquerade universe, was released on 27 April 2022.
At Sharkmob, we are committed to building an inclusive team that represents diverse backgrounds, perspectives, and skillsets – because we believe that helps us create great games. We welcome all candidates who are aligned with our core values of shared ownership, smart decisions, and, last but not least – having fun! We hope you want to join us on our adventure and become a part of our crew. You can find more great perks of being a crew member. If you want to know more about Sharkmob and our projects, visit our homepage. Visa mindre

På LFV gör vi just nu en förändringsresa med ny teknik, nya förutsättningar och ett ökat ansvar. Vi växer som organisation och söker därför dig som vill vara med och forma framtidens flygtrafiktjänst. Hos oss kan du vara med och bidra till smarta lösningar för morgondagens flyg.

LFV är Sveriges ledande aktör inom flygtrafikledning för civil och militär luftfart med tillhörande tjänster. Våra flygledare leder dagligen cirka 2 000 flighter i svenskt luftrum. LFV var först i världen med flygtrafikledning på distans och vi fortsätter att driva digitaliseringen. Genom olika samarbeten är vi med och effektiviserar det europeiska luftrummet. LFV har 1 100 anställda och en omsättning på 3,3 miljarder kronor. Läs mer om LFV!

Avdelningen Forskning, Innovation och Digitalisering, FoID, ansvarar för det koncernövergripande och långsiktiga arbetet med digital transformation inom LFV samt forsknings- och innovationsverksamhet för att stödja myndighetens utveckling och anpassning till en allt mer digitaliserad omvärld.

Inom avdelningen har enheten Forskning och Innovation (FoI) ansvar för att driva LFVs forskningsverksamhet. Det innefattar att ta fram beslutsunderlag för initiering av forskning, säkra extern finansiering för forskning, driva och följa upp forskningsprojekten samt leverera resultat som skapar största möjliga nytta för LFV och luftfarten i Sverige. Forskningen bedrivs till stor utsträckning tillsammans med våra kunder samt med aktörer från industri och akademi. FoI deltar i internationell samverkan genom bl.a. SESAR JU och COOPANS rörande ATM-utveckling i Europa. FoI har också en aktiv roll som ledamot i Trafikverkets forskningsportfölj för luftfart, för att bidra med behovsbild samt utgöra råd till Trafikverket kring forskningsfrågor inom luftfartsområdet.

Inom enheten FoI finns idag ca 25 medarbetare med specialistkompetens inom projekt- och programledning, ingenjörer och specialister inom områdena HF (Human Factors), ATM (Air Traffic Management, RTS (Remote Tower Services, och UTM (Unmanned Traffic Management), Validering och Visualisering. Inom respektive område/kompetensgrupp har vi en teamledare som samordnar och koordinerar arbetet. Vi har idag en gruppchef och utökar nu med ytterligare en gruppchef.

LFV söker dig som vill vara med och leda utvecklingen av framtidens flygtrafiktjänster.

Din roll:
Som Gruppchef ansvarar du och arbetar med följande delar:


• Verksamhets-, budget- och personalansvar.
• Effektiv försörjning av kompetens och resurser för forsknings- och utvecklingsprojekt inom sitt område (med interna och till viss del externa resurser)
• Säkerställa att medarbetare har förutsättningar för leveranser av rätt kvalitet och i rätt tid
• Utveckla och förbättra/effektivisera verksamheten
• Samordna och koordinera arbetet med respektive teamledare

I och med att våra medarbetare finns på flera orter kommer det beroende på grupp innebära regelbunden närvaro på något/några av följande tjänsteställen: Sturup, Norrköping och Arlanda. I rollen som gruppchef kommer du ansvara för 10-15 personer beroende på ort och uppdelning av kompetensgrupper/arbetsområden.

Som gruppchef ingår du i ledningsgruppen för enheten. 

Din profil
Du har en relevant akademisk examen eller likvärdig arbetslivserfarenhet och 5 års erfarenhet från komplex tekniskt orienterad verksamhet. Du behöver också ha flerårig erfarenhet av verksamhets-, budget- och personalansvar.

Har du erfarenhet av flygbranschen och från statliga myndigheter är det meriterande, men inget krav. Du behöver också kunskaper i engelska i tal och skrift. 

Du har en helhetssyn och förstår andra funktioners utmaningar genom att lyssna in och samarbeta för att på bästa möjliga sätt möta LFVs övergripande behov. Du förstår vikten av att arbeta tvärfunktionellt, att utveckla goda relationer och skapa engagemang inför en uppgift genom tillit och att både ge och ta emot feedback. Med ett tydligt ledarskap säkerställer du förståelse hos dina medarbetare för hur deras roll och prestation hänger ihop med funktionens gemensamma leverans och LFVs övergripande mål. Du förstår vikten av att aktivt kommunicera och tydliggöra förväntningar på medarbetares prestation i syfte att skapa delaktighet och mening.

Vi lägger stor vikt vid dina personliga egenskaper.

Vi söker dig som har ett intresse av att leda människor i en tekniskt orienterad verksamhet.

Anställning och förmåner
Tjänsten är en tillsvidareanställning med placering i Norrköping, Sturup eller Arlanda. Innan anställning genomför LFV en säkerhetsprövning som bland annat innefattar registerkontroll, säkerhetsintervju och drogtest. Denna tjänst kräver svenskt medborgarskap.
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LFV har goda anställningsvillkor och ett brett utbud av förmåner som bland annat innefattar en privat sjukvårdsförsäkring och goda pensionsvillkor. Visa mindre

We are looking for a Medical Affairs Director with a passion and creativity to develop great drugs for oncology related conditions. You will join a journey in building and growing the company aiming at improving the lives of patients with rare oncology related diseases.
With direct report to the Chief Medical Officer, you will be responsible for medical affairs activities for two programs within the clinical development and commercialization stages. You will be a key player in a fast-growing cross-functional team and work closely with the Chief Commercial Officer, Director of Regulatory Affairs, the Project Director, Director of Clinical Operations, and colleagues across the organization.
Your main tasks
Responsible for developing and executing the medical affairs strategy for two orphan oncology programs. Ensures cross-functional alignment and organizational support for the medical affairs program.
Act as disease expert. Activities range from internal training, seeing that external questions are addressed, and providing informational services to health care providers in the community with focus on the US.
Manages and tracks implementation of publications plans, and the reporting of trial results at scientific meetings and through journal articles.
Manages Scientific Advisory Board activities, provides information and other support to persons who are recognized experts in their fields, as well as supports thought leader development.
Involvement in all stages of clinical development including study design, initiation, and oversight.
Provide strategic input on the design and implementation of investigator-initiated trials.
Act as liaison to health care professionals and professional organizations, and disease state and clinical guidelines advocacy groups. Supports the efforts of professional associations, patient support groups, and educational foundations.
Contribute to product development, launch preparation and execution, provides medical review/approval of promotional materials for scientific meetings, symposia, and other Medical Education activities, in accordance with applicable Codes of Practice and regulations.
Supports development of material and dialogue with payers and reimbursement policy makers.
Assists in the development of lifecycle management plans and new claims and preparing responses to competitor actions and communication.
Collaborate with regulatory colleagues and legal consultants to ensure that all written documents are accurate and adhere to the guidelines mandated by regulators.
Assists in writing and amending SPCs (Summary of Product Characteristics), PILs (Patient Information Leaflets) and label information.



Your qualifications
To master the position as Medical Affairs Director, we believe that you have at least five years of industry experience and preferably that you, when it comes to therapeutic areas, have experience from oncology related conditions. You have a medical degree (M.D.) or equivalent educational background.
We also believe that you have:
Good knowledge of global healthcare systems, including US.
A high level of knowledge of regulatory environment including key regulatory agencies and approval processes, including US.
Previous work and leadership experience in international and multidisciplinary drug development teams and broad understanding of drug development process.
Understands preclinical, clinical, regulatory, and commercial functions, as well as business strategy and business requirements.

As a colleague, professional and director you:
Have cross-functional team and relationship enhancing skills, with the ability to listen and consult with others, recognize and reward others contribution and build team spirit
Possess very good networking skills, with the ability to communicate effectively with people on different levels, and an ability to manoeuvre between conflict management and disarming situations with a sense of humour.
Demonstrate an outstanding ability to interpret and evaluate scientific, competitive and business-related information critically and objectively.
Are comfortable with presenting information, speaking with stringency, expressing key points and arguments clearly
Possesses a strategic mindset with the ability to see the big picture and demonstrates accountability for a wide range of issues bringing the organization closer to its goals
Delivers high standard with regards to quality and quantity, achieves project goals and focuses on stakeholder needs and satisfaction
Have an entrepreneurial mindset – keeps up to date with competitor information and market trends, identifies business opportunities and demonstrates financial awareness

Other information
Travelling: The position will require travelling up to approx. 30%.
The head office is in Malmö (The Point, Hyllie) and you are preferably able to work primarily from there; other locations considered depending on the candidate. There is an opportunity to work partly from home.
How to apply
Please submit your resumé and cover letter, along with any other material as soon as possible, but no later than December 31st. All applications must be in English and are treated confidentially.
Candidates will be assessed as applications are received. Only candidates considered will be contacted
For more details about the job or the company, please contact Carl Bjartmar, Chief Medical Officer. Phone +46 (0)703 00 12 22 or email [email protected]
What we offer
At Ascelia Pharma, your skills, dedication, and engagement help us improve the lives of people living with cancer. We offer you an opportunity to be part of a fast-growing company with global reach, where engagement, dedication and results are met with opportunities for individual and professional development.
Join us on our journey to improve patients’ lives and build a global orphan oncology life science organization. Visa mindre

Regulatory Affairs & Quality Assurance Manager to Niconovum

Do you thrive on challenges and want to be a key player in our growth journey? Would you like to be part of the entire product cycle, from registration to marketing and launch? Do you have experience with pharmaceuticals but is looking to put this to use in a smaller, more flexible, and agile workplace, which will allow you to drive your own initiatives, build upon your strengths, and explore your limits?

Look no further - Niconovum AB is looking for a new Regulatory Affairs & QA Manager.

The company
Niconovum AB is a medical company that markets innovative nicotine replacement therapy (NRT) products under the Zonnic brand. Our products are sold in four markets: Sweden, Norway, Finland and Iceland, and our brand is third in terms of market share in each Nordic market it competes in. All products are regulated and approved pharmaceuticals.

The role
As RA & QA Manager, you will be based in our Hyllie office and report directly to the CEO. You will also interact with all internal and external stakeholders and parties – so you must have excellent communication skills and the ability to create and maintain good relationships.

Your main goal is to ensure regulatory and quality compliance for existing products, while supporting product development and geo-expansion activities in all matters related to quality and regulatory affairs. This includes product regulatory approvals, variation applications, change control, risk assessments, supplier quality management, and launch strategies – as well as management reviews, SOP´s, and inspections. You are also expected to become the company´s Responsible Person for GDP, either directly or after training.
To your support you will have colleagues and external consultants with expertise within NRT, formulation, CMC, pharmacovigilance, project management, RA and QA.

In short, your responsibilities will be to:

• Maintain and update regulatory dossiers, as needed
• Manage regulatory strategies for new product approvals, line extensions or expansion into new markets
• Manage approvals and registration of artwork
• Maintain Quality system, manuals and policies
• Ensure documentation of relevant activities and processes
• Ensure the safety and quality of all products throughout the production and distribution processes
• Handle consumer and customer questions and complaints
• Act as the local pharmacovigilance manager and support to QPPV
• Coordinate all internal and external inspections and audits
• Evaluate new GxP partners and quality agreements
• Ensure wholesale distributor obligations are being met
• Support to the manufacturer´s QP
• Manage the department budget

To succeed in this role, we think you have:

• A Bachelor´s or Master´s degree in a relevant field, preferably within pharmacy
• 3+ years in Pharmaceuticals, handling regulatory issues and related documentation
• Experience with GDP/GMP/GVP
• Excellent communication skills both written and verbal
• Proficiency in both Swedish and English

But above all, we value the right personality and attitude – and this means a balance between structure and flexibility; a strategic mindset with operational hands; an analytical approach paired with a solutions-oriented mentality. As we nurture our suppleness and adaptability, we would like for you to embrace the possibility to take a holistic view while also rolling up your sleeves and dive into the practical details, to take initiatives and stand up for them, and educate others along the way.

Are you ready?

This process is in collaboration with Badenoch + Clark. For any questions regarding the position, please reach out to Senior Consultant Matilda Rodey at [email protected].
We look forward to receiving your application as soon as possible and no later than June 13th, at www.badenochandclark.se or using link below. Selection will be ongoing – so contact us today! Visa mindre

We believe that the work we do at QPharma makes a difference, as the products that we develop and manufacture help to improve the health of people across the world, including those living in developing countries. This is done through collaboration with many different non-profit organisations.

The company offers a creative environment, with many opportunities for personal growth and development.

?The laboratory
As head of QC you will have the overall responsibility for all activities within the Quality Control laboratory consisting of the following areas; Analytical Development, Analytical Support, Starting Material & Enviornmental Monitoring and System & Equipment. The department is continuously growing and consists of approx.. 42 employees covering Technicians, Analytical Scientists and Chemists.
The laboratory supports most of the chemical analyses and there are plans in place to also support microbiological analyses in the future.

Responsibilities

* Lead and develop the QC department together with the personnel
* Develop a long- term strategic roadmap together with the Executive Management and your QC Leadership Team
* Responsible for executing both operational and strategic objectives
* Support development projects and commercial production with resources and deliver according to project- and production plans
* Responsible for keeping an adequate quality level and setting the overall direction and provide guidance in quality matters ensuring compliance and at the same time keeping efficiency
* Develop the organization, system and routines to meet current and future requirements
* Take the lead in the digitalization of the lab, i.e. re-think the way work is conducted in a lab using digital tools such as LIMS, CDS and other computerized systems within the lab
* Apply and maintain a LEAN mindset e.g. indentify and implement value adding activities and eliminate waste
* Represent QC during inspections from health authorities (EMA, FDA or others) and from customers
* Participating in one or two of Qpharmas management teams; production and projects


Qualifications
We believe that you hold a M. Sc. and/or PhD degree in chemistry or analytical chemistry or equivalent and have profound experience (at least 10 years) in the pharmaceutical industry as Head of QC or a similar position.

* You are experienced working in a regulated environment and have extensive knowledge and experience with GMP and ICH guidelines
* Experience of managing staff, preferably also through other managers
* Experienced in handling day to day operational matters with strong decision-making skills
* General knowledge in method validation and equipment qualification
* High technical skills including very good knowledge of QC equipment and computerized systems
* General knowledge in the field of sampling of starting material, environmental monitoring and microbiological requirements related to GMP production
* Proven track record of representing the company and QC during Audits from FDA or local authorities
* Very good written and verbal communication skills in Swedish and English

We strongly believe that your personal characteristics are very important to be a successful leader at QPharma. Our expectations are:


* High capacity and sense of ownership, high drive with a can-do attitude, positive personality and with high level of engagement
* Excellent communication skills, flexible and dynamic leadership style creating commitment and treats people with respect
* Strong and engaging people manager who brings people on board
* Ability to build relationships and teams with a high level of trust
* Solution driven mindset, takes decisions and get things done
* Good at delegating and sharing responsibility and tasks, while providing support
* Strong ability to think strategic and see things from a holistic perspective
* You have the ability to keep calm in stressful situations with high pressure
* You have very high collaboration and stakeholder management skills

Important that you share our values:

* Make difference
* Close customer
* Best workplace

Examples of engagement at QC connected to QPharma values:

* We help each other and share knowledge
* We show respect and honesty
* We show appreciation and give each other positive feedback
* We see opportunities and work to improve things to the better


To read more about us please visit our website www.qpharma.com .

Application
In this recruitment we collaborate with Experis Executive. If you have any questions or other inquiries please refer to Experis Executive Recruitment Consultant Patrik Nordberg at +46 40 6606355 or [email protected] . Please apply as soon as possible as selection is ongoing.

For contact with union representatives please contact Anna Ejdemo at Unionen at 040-361890 or Maria Nilsson at Akademikerförbundet (SSR) at 040- 361961.

We look forward to your application! Visa mindre