Ajankohtaista

Field Service Specialist, Molecular Diagnostics and Life Science – QIAGEN

https://www.linkedin.com/jobs/view/3026782865

About the job

Your Tasks

• In your role you are focused on field- and office-based, post-sale technical support to all QIAGEN customers and are responsible for on-site repairs, installations, customer training, education and/or troubleshooting on QIAGEN instrumentation, including consumables and applications in all markets as well as coordinating with other internal departments to optimize protocols or aid in experimental design.
• You develop and maintain highest possible level of technical knowledge of automation / instrumentation as well as related applications and provide second-tier support for Sales and Technical Support by performing trainings such as train the trainer, seminars for internal and external customers
• You actively promote QIAGEN products including Service and Support products and assist in exceeding revenue targets, support demonstrations and evaluations if needed and give active feedback to Sales, Marketing, Global Product Support, Global Training and Management
• You utilize all available tools such as Service Reports, Spare Part & Service Manuals, ISI Notes, and the relevant databases to input information that will increase effectiveness
• You will be required to work with hazardous substances such as acids and solvents and to work in biological laboratories up to BSL3

At the heart of QIAGEN are our people who drive our success. We act with passion, always challenging the status quo to drive innovation and continuous improvement. We inspire with our leadership and make an impact with our actions. We create a collaborative, safe and engaging workplace which forms the basis for high performing individuals and teams. We drive accountability and entrepreneurial decision-making and want you to excel your growth and shape the future of QIAGEN.

QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.

Desired Skills and Experience

• You bring a M.Sc. or Ph.D. degree in molecular biology or genomics
• You have an extensive practical/laboratory experience of the most frequently used techniques, or at least 2 years as a technical service or field service specialist within a relevant market sector
• Your are known for your experience with diagnostic equipment technologies and applications; experience with CRM programs and web-based tools to retrieve and analyze data is a plus
• You are a self-starter with the ability to handle and manage multiple tasks in a result-orientated commercial environment and are fluent in English and Finnish; fluency in another European language is a plus.
• You like to travel (70%) and bring a valid driver´s license and passport

Data Scientist – Nightingale Health

https://www.linkedin.com/jobs/view/3044690812

About the job

Do you want to make discoveries that power the future of preventative healthcare?

Nightingale Health is looking for a Data Scientist to join our team. Our blood test technology simultaneously measures different molecules that capture a diverse range of metabolic processes. We have used it to profile a million samples from the world’s largest research studies, and linked those results to extensive clinical data and health outcomes. We use machine learning to discover new insights into human health from these data.

Sounds interesting? Read on.

Here’s what you’ll do:

• Hands-on data analysis in a globally unique dataset of molecular and clinical measurements to build models that predict people’s future health risks and identify how they can improve their preventative health.
• Work with other data scientists and software engineers in an agile environment to bring new discoveries into our products.
• Carry out bespoke analysis for clinical partnerships using our technology to evaluate a wide range of preventative health care applications, including clinical trials.
• Write clean, readable code for your own analysis and to be used as the basis for future products.
• Communicate internally and externally about how our rigorous science underpins our products.
• Bring new ideas on how to make our health insights more understandable and exciting for customers.

You’ll be a perfect fit if you:

• Have studied and/or worked on data science before, and are excited about learning new things from big datasets.
• Have an MSc or PhD in a scientific field like bioinformatics, biomedicine, data science, epidemiology, or statistics.
• Can work in a fast-paced environment with a focus on translating new science into products.
• Can clearly communicate scientific findings to both expert and lay audiences.
• Want to make a difference in building better preventative healthcare.

We also value:

• Real-world data science experience, including data acquisition, cleaning, modelling, and interpretation.
• Knowledge of the R and Python programming languages.
• Experience with large-scale metabolomic or genomic datasets.
• Understanding of molecular biology and medicine.
• Diverse backgrounds! Don’t worry if you don’t exactly match these requirements; we’d still like to hear from you.

What we offer:

• Meaningful, pioneering work that offers you the opportunity to constantly develop your skills.
• A unique opportunity to work in an international and multidisciplinary team of scientists, developers, designers, and biotech business experts.
• Responsibility and independence as an accountable member of our Data Science team.
• Premium health and travel insurance (valid during and outside working hours) on top of the mandatory occupational health package.
• Full fringe benefits for health and well-being, including massage, dental care commuting, sports, and culture.
• An industry competitive salary.
• A flexible and informal working environment with both professional office capabilities as well as remote working possibilities.
• An in-house chef and café that serves warm lunch every day.
• Team get-togethers.
• Interest clubs from running to music (we have an in-house band!)

This is a full-time position based in Helsinki.

Your next steps

Step 1: Follow the link below and fill in your information along with your CV and a cover letter.

Step 2: Have a video chat with our Chief Scientific Officer Jeff Barrett.

Step 3: Complete our data science assignment, which will be reviewed by the team.

Step 4: Meet Jeff, and other members of our team at an in person interview.

Step 5: Meet our CEO Teemu Suna for the final interview.

The position will be filled as soon as the right candidate is found.

Want to know more?

In case you have questions, feel free to mail our recruiting team at people [at] nightingalehealth.com

A bit more about us

Nightingale Health is The Preventive Health Company. Staying healthy is one of the top priorities in human life. Our health has a profound impact on our quality of life, and it’s also strongly connected to the lives of those close to us. Health is, eventually, about all of us – healthy citizens have the power to fuel entire societies to prosperity. Nightingale Health enables prevention by combining the power of our in-house developed, advanced blood analysis technology with unprecedented access to global health repositories and world-leading medical research. With this combination, we go beyond the traditional healthcare and wellbeing tools: We provide the scientific connection to multiple health and disease outcomes and the ability to predict future healthy years.

Research Assist-ant/​Doctoral Researcher and Postdoctoral Researcher – University of Helsinki

https://www.linkedin.com/jobs/view/3049271132

Job Description

The groups of Research director Mart Saarma and Docent Maria Lindahl at the Institute of Biotechnology, HiLIFE, at the University of Helsinki invite applications for the position of 1) a research assistant/doctoral researcher and 2) a post-doctoral researcher for a fixed term of 2 years starting June 1st, 2022, with a possibility for continuation.

The groups have previously identified a neurotrophic factor MANF, as a protective and regenerative factor for pancreatic beta cells (Lindahl et al, Cell Reports 2014, Hakonen et al., Diabetologia 2018). The groups received funding from the Juvenile Diabetes Research Foundation (JDRF) for two projects aiming at studying the effect and safety of MANF and MANF mimetics in beta cell protection and regeneration in vitro and in vivo type 1 diabetes models.

We are looking for applicants with 1) a M.Sc. degree or comparable and 2) a PhD in biology, biochemistry, genetics, biotechnology, pharmacy or equivalent, and a keen interest in the research field of diabetes and diabetic mouse models. Successful candidates are expected to have experience in laboratory work; cell culture, cell biology, PCR techniques, protein biochemistry techniques. Competence to carry out procedures with laboratory mice is considered a benefit. Ability to work independently and as part of a multidisciplinary research team is required as well. Good written and verbal communication skills in English is also necessary.

Further degree requirement for doctoral researcher position: The appointee must apply, and obtain, the right to pursue a doctoral degree at the University of Helsinki within the probationary period of 6 months: https://www.helsinki.fi/en/admissions-and-education/apply-doctoral-progr…

Further degree requirement for postdoctoral position: The degree requirement must be met by the beginning of the employment.

The work includes isolating Langerhans islets from mouse pancreases and testing regeneration-promoting effects of proteins and chemical compounds on islets in vitro and in vivo in type 1 diabetes mouse models.

The Application Should Include

• A motivation letter (max. 1 page), clearly stating why you consider yourself a good candidate for the position.
• CV including prior laboratory work/research experience and list of publications.
• One or more recommendation letters or names and contact information of reference

The salary is based on the salary system of the Finnish Universities for teaching and research staff for the doctoral and postdoctoral positions; research assistant position follows the salary system for specialist and support staff. In addition, the appointee will be paid a salary component based on personal work performance.

A trial period of 6 months will be applied.

Please, submit your application by May 10th, 2022, together with required attachments through the University of Helsinki electronic recruitment system by clicking on the ”Apply for job” button. Internal applicants (i.e., current employees of the University of Helsinki) submit their applications through the SAP Fiori portal.

More information about the work carried out by the team can be found at: https://www2.helsinki.fi/en/researchgroups/neurotrophic-factors-and-rege… and questions can be addressed to maria.lindahl@helsinki.fi.

University of Helsinki

The University of Helsinki is the largest university in Finland and one of the leading multidisciplinary universities in the world. International experts working at the University are also attracted by Helsinki’s unique atmosphere and Nordic lifestyle. The University of Helsinki offers comprehensive services to its employees, including occupational health care and opportunities for professional development. Further information at www.helsinki.fi/en/about-us/careers.

Helsinki Institute of Life Science (HiLIFE) supports high quality life science research across the University campuses and faculties. HiLIFE builds on existing strengths and new recruits and partnerships to create an attractive international environment for researchers to solve grand challenges in health, food, and environment.

Institute of Biotechnology (BI) is an internationally renowned research institute with an inclusive and curiosity-driven working culture. Using cutting-edge infrastructures we advance breakthrough discoveries, technology development and innovations. https://www2.helsinki.fi/en/hilife-institute-of-biotechnology

Due date

10.05.2022 23:59 EEST

Application Details

To Apply: Please use the ”Apply” Button Below or see the Job Description Above

When inquiring or applying for this job opening, please also reference AcademicCareers.com.

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Medical Advisor, Respiratory Finland – Sanofi

https://duunitori.fi/tyopaikat/tyo/medical-advisor-respiratory-finland-scsom-14833984?utm_source=loimu&utm_medium=email

Our team:

Join Sanofi Finland as Medical Advisor Respiratory. In this role, you will implement the country medical affairs plan and other key medical affairs initiatives in collaboration with internal and external stakeholders, in alignment with the Respiratory North Europe medical strategy, and according to the highest ethical and compliance standards.

Travel expected in this role is approx 20%. This is a permanent role.

Main responsibilities:

• Be a strong partner to the local Commercial, Market Access, Regulatory, Pharmacovigilance and Public Affairs, and provide continuous medical advice and training. Support local market access medical alignment and new indication launch preparation. Provide input to local medical budget
• Drive development and execution of local Medical Affairs plan as well as local communication strategy in alignment with the Respiratory North Europe medical strategy
• Conduct internal and external medical education to enhance disease and product knowledge and awareness. Regular external scientific/medical presentations, e.g. scientific conferences, high-level scientific or business audiences. Maintain and develop strong relationships with KOLs and health authorities
• Oversee and interpret new scientific data, literature, competitive trends and product opportunities and adjust medical and educational activities accordingly. Support to all company sponsored clinical trials
• Drive, coordinate, support and ensure regular follow up of medical -, investigator initiated – and other research projects, including driving approval processes
• Drive organization and implementation of Advisory Boards and other scientific meetings

About you

• Academic scientific or medical degree, Pharm D, MSc and/or PhD in life sciences, or equivalent
• Knowledge of the pharma/biotech industry
• Relevant experience in a healthcare environment
• Clinical study and/or project management experience
• Experience from a Medical Affairs position in the pharmaceutical industry is desirable
• Self-motivated, organized and being able to work independently
• Ability to adapt to new procedures and software
• Capability for continuously update and follow scientific literature of relevance
• Excellent presentation skills and proficient in public speaking
• Possesses integrity and self-awareness
• Analytical whilst able to retain a broad perspective
• Ensures that projects, assignments, and deadlines are completed on schedule
• Excellent command of both verbal and written English and Finnish
• Driver’s license is required

Pursue progress. Discover extraordinary.

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

#LI-EUR

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

Account Manager Genomics/NGS, Finland – PerkinElmer, Inc.

https://www.linkedin.com/jobs/view/3001150685

About the job

PerkinElmer’s commitment to scientific innovation is at the heart of everything we do. In PerkinElmer meaningful work arises to a whole new level. We help customers make smarter decisions, earlier diagnoses, more effective treatments and scientific breakthroughs.

Now we are looking for an Account Manager Genomics/NGS in Finland

The Account Manager will be responsible for achieving business targets, through sales development and field marketing programs, for the PerkinElmer Applied Genomics product portfolio in Finland, as well as supporting the business development of the NGS market in the Nordics.

Key Responsibilities

• Competes for all Genomics, Proteomics, and Biologics sales opportunities throughout Finland
• Builds and maintains strong customer relationships
• Constantly attempts to secure business in new accounts and follows customer account receivables
• Provides accurate monthly forecasting, updates, and next steps within SFDC on a weekly basis as well as timely, accurate and competitive pricing to customers, and submits internal approval requests
• Attends seminars, exhibitions, and demonstrations to promote business
• Maintains knowledge of PerkinElmer products, as well as knowledge of competitors’ products, prepares, documents, and updates PerkinElmer presentation aids accordingly
• Supports the account managers in the rest of the Nordics with insight and technical expertise on the NGS products and workflows
  

Your Profile

• Bachelor’s or Master’s degree in Science, preferably in Biology, Molecular Biology, or Biochemistry
• Strong experience within the Biotechnology, clinical diagnostics, or Life Science markets with a solid network in the sector.
• Strong background and knowledge base within NGS workflows and reagents.
• Results driven, energetic, effective, a self-starter with a strong motivation for sales
• Excellent in verbal and written communication and presentation skills, and who can excel in an international sales environment
• Independent, with good organizational and teamwork skills, driving you to continuously seek new opportunities
• Flexible and able to communicate with colleagues and customers locally and internationally
• Willingness to travel across all of Finland and the Nordics, and occasionally across Europe. Most customers are in the southern part of Finland, and candidates located in the southern part of Finland will be preferred
• Desire to learn, grow, and take the lead in a sales role within a fast-paced matrix organization
• Fluent in Finnish and English, both verbal and written
  

What We Offer

• Inspiring leadership and exceptional employees
• Dynamic and innovative culture
• Focus on career development with both local and international career opportunities
• Collaborative and diverse environment
  

For further information, please contact Nordic Life Science Leader Christine Regnell (christine.regnell@perkinelmer.com). Please note, that we will start interviews as soon as we find suitable candidates.

Join us today – For the better!

PerkinElmer is a drug free employer and a medical examination for new employees includes a drug test.

Product manager II / Sr PM (oncology)

Apply here

Senior Project Manager – Oncology, EMEA based role

Come discover what our 25,000+ employees already know: work here matters everywhere. We’re a growing and evolving biopharmaceutical industry leader, which means you’ll have endless opportunities to work with experts around the world and build the career you’ve dreamed of.

As a part of the Syneos Health team, you’ll help us deliver results for a rewarding reason – we improve patients’ lives around the world. Because to us, a patient isn’t just a number, they’re our family, friends, and neighbors.

Why Syneos Health

#SyneosHealthLife means we’re committed to our Total Self culture – where everyone can authentically be themselves. Our Total Self culture is what unites us globally, and we know every person’s unique contributions make a difference.

We believe our success is a direct result of the people who are driving it – you! We value your dedication to care for our customers and patients, so we want to focus on taking care of you. That’s why we offer a comprehensive benefits program encompassing your total health – physical, mental and financial.

We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.

Equal Opportunities Plan. Its objective is to achieve the principle of equality of opportunity in Syneos Health’s employment practices ensuring that our workforce is truly representative of each gender and that every employee is respected and is able to work under equal conditions.

Job responsibilities;

The position provides customer focused leadership in managing and delivering the operational and financial aspects of one or more clinical projects from proposal development to final deliverables and ranging in size and complexity from single service studies to full scope, multiple protocol projects and/or global projects across various phases and functional areas with limited interaction from supervisor. May oversee less experienced Project Managers (PMs) and have line management responsibilities.

Project Leadership And Delivery

• Manages a project as Project Manager overseeing interdisciplinary clinical research programs ensuring compliance with Good Clinical Practices (GCPs), relevant Standard Operating Procedures (SOPs) and regulatory requirements.
• Acts as primary liaison between the Company and the Customer to ensure project launch, conduct, and closeout according to the Customer’s and the Company’s contractual agreement.
• Leads clinical team to ensure quality, timelines and budget management.
• Accountable for the financial performance of assigned projects
• Accountable for all project deliverables for assigned projects and/or project regions.
• Coordinates activities and deliverables of all project conduct partners and proactively identifies and manages issues.
  

Reporting And Communication

• Accountable for maintenance of project information on a variety of databases and systems.
• Maintains and evaluates project progress by maintaining timelines and other tracking/analysis tools.
• Responsible for project management components of inspection readiness for all aspects of the project conduct, including Trial Master Files.
• Provides oversight for development and implementation of project plans in accordance with Controlled Documents.
• Independently prepares, coordinates, and presents project material at internal and external meetings.
• Directs the activities of assigned Project Support staff; line manages and mentors other project management team members and clinical staff; facilitates team building and communication.
• Prepares project management reports for clients and management.
• Implements resource strategies to achieve project goals.
• Develops contingency planning and risk mitigation strategies to ensure successful delivery of project goals.
  

Business Development

• Participates in bid defense meetings where presented as potential project manager/director.
• Develops strong relationships with current clients to generate new and/or add-on business for the future.
• Keeps a current awareness of business unit’s and assigned projects’ therapeutic environment and drug development trends
  

Management

• May train and support new Project Managers. Facilitates team training in accordance with protocol and/or project requirements, including therapeutic, protocol specific, and process training.
• May be required to line manage other project management team members and clinical monitoring staff
  

Qualifications

What we’re looking for;

• Bachelor’s Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or related field or equivalent combination of education and experience.
• Strong knowledge of Good Clinical Practice/ICH guidelines, regulatory requirements, drug development process and clinical monitoring procedures.
• Clinical research organization (CRO) and relevant therapeutic experience preferred.
• Strong ability to manage time and work independently.
• Ability to embrace new technologies.
• Excellent communication, presentation, interpersonal skills, both written and spoken
• Flexibility and the ability to mentor and manage new staff and to handle multiple tasks to meet deadlines delivering high quality work in a dynamic environment.
• Ability to travel as necessary (approximately 25%).
  

Get to know Syneos Health;

We are the only full-service biopharmaceutical solutions company in the world. That means we bring together the best clinical and commercial minds to create a better, smarter, faster way to get medicines into the hands of patients who need it most. Learn more about Syneos Health.

Additional Information;

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities.

Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above.

Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms.

Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Syneos Health is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Syneos Health is willing to provide reasonable accommodations required for a medical condition or disability.

Technical support specialist, qPCR: Oulu, Finland

Link to the job

Technical Support Specialist, qPCR: Finland

For an innovation based Life-Science Research company, a global leader in the field of developing most advanced technologies in Molecular Diagnostics sector, we are currently looking for an Technical Support Specialist who will provide training, demonstration & technical support on their state-of-the-art qPCR systems to the lab professionals in(bio) pharmaceutical, Hospitals, CROs & Academia research sector.

Region – Oulu, Finland

Requirements:

• Masters in Molecular Biology, Biochemistry or similar streams
• Hands-on experience with qPCR is a must have
• Fluent Finnish & English
• Living in or willing to relocate to Oulu in Finland

Should you like to find out more about the function please get in touch with Paurush Dhiman via LinkedIn.

NonStop is one of the largest and fastest growing specialised life-sciences & Med-tech recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences for all EU8 countries. Please visit our website for a full list of the niche markets we cover

Key account manager, haematology-oncology (Remote – Nordics)

Apply here

Job Description

Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases – often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines and novel product candidates, from early- to late-stage development, in neuroscience and oncology. We actively explore new options for patients including novel compounds, small molecules and biologics, and through cannabinoid science and innovative delivery technologies. Jazz is headquartered in Dublin, Ireland and has employees around the globe, serving patients in nearly 75 countries. For more information, please visit www.jazzpharmaceuticals.com and follow @JazzPharma on Twitter.

Are you experienced in sales within the life science industry and looking for a Nordic opportunity within hematology/oncology?  Do you want to play a key role allowing you to have a positive impact on the lives of patients and their families by taking part in our exiting pursuit as we build our Nordic organisation and strive to serve many more patients with rare diseases in the Nordics?

We are looking for a self-driven, scientific, and digitally savvy person taking the lead for the Nordics within haematology/oncology as we are looking to expand our footprint in the Nordics.

The Jazz Commercial Ambition is to be the #1 partner of all HCPs involved with Jazz, be trusted, and recognized for our empathy, agility and relevance of action. Our KAMs play a pivotal role in fulfilling our commercial ambition. As such, the Jazz Vision for our KAMs is to be a cornerstone of Jazz interactions in-field and to be accountable for the definition and coordination of personalised, targeted, multichannel HCP engagement strategies to maximize outcomes for HCPs and patients along with the commercial development of our Jazz portfolio

Brief Description:

The role of the Nordic Key Account Manager (KAM) is to maximise the full sales potential of the Haematology/Oncology (H/O) product portfolio in the Nordics, achieving sales and related performance targets (as defined by the management team). This will be achieved through coordination and collaboration with internal and external stakeholders to ensure the appropriate patients have access to Jazz Pharmaceuticals H/O products. Developing professional working partnerships with relevant stakeholders to positively influence sales potential, future guidelines, funding, positioning of products and ensure effective implementation of peer to peer/advocacy programs.

The Nordic KAM will take full accountability for the preparation and execution of strong territory business and key account management plans as agreed with the management team, fully utilizing agreed processes and procedures.

Essential Functions

• Deliver sales and related objectives against targets
• Develop a partnership relationship with KOLs and stakeholders by being an expert in the Jazz Pharmaceuticals products and relevant disease areas as well as local/regional and national healthcare policy as appropriate
• Build customer networks that enable the rapid identification, diagnosis and treatment of patients
• Collaborate with market access on local and national reimbursement
• In close cooperation with the H/O Brand Manager; medical affairs and your manager develop, implement, and review cross-functional country and key account business plans for H/O Nordics which are aligned with the Nordic strategy and the H/O brand strategy plans. The plans are to be endorsed by the GM and the H/O Brand Manager.
• Monitor and evaluate performance against business plan and deliver within agreed matrix of activity (effective account call coverage and frequency) and budget (appropriate use of promotional spend) as agreed with the manager
• Work with medical, market access and marketing to enable customer access to Jazz Pharmaceuticals support programmes e.g., educational events, relevant symposia, peer to peer programmes
• Identify and capture opportunities for business growth e.g., key account potential, new projects or added value services
• Profiling (and regular updating of) key customers and accounts into currently available CRM system
• Accurate and timely reporting of customer and business records, through CRM system, using agreed performance measures
• Willingness and ability to assist with ad hoc business projects as defined and directed by the GM and/or the manager
• Behave ethically, responsibly, and professionally in accordance with Jazz Pharmaceuticals values and Nordic codes of practices

Required Knowledge, Skills, and Abilities

• Previous knowledge and experience of disease area essential
• Previous speciality pharmaceutical sales experience ideally with a proven track record in H/O or orphan disease area in at least one of the Nordic countries. Preferably outside of Denmark.
• Genuine interest in working across borders and with Nordic HCPs
• Experience in working cross-functionally; self-starter with a strong sense of personal accountability as well as the ability to work in a cross-functional team in a dynamic environment.
• Efficient and skilled in working digitally with customer engagement
• Proven track record in negotiating and influencing within a healthcare setting to deliver agreed and measurable objectives
• Effective and persuasive communicator with excellent presentation skills
• Ability to access funding for new and existing drugs, with a demonstrable understanding of funding processes
• Advanced account management skills that demonstrate business acumen and an innovative approach to projects and solutions that bring added value to Jazz Pharmaceuticals and other stakeholders
• Experience in working with appropriate partners on joint projects that deliver benefits to all stakeholders, in particular patients

Required/Preferred Education and Licenses

• Bachelor’s degree
• Fully valid driving license
• Strong written and verbal communication skills (In English and one of the Scandinavian languages)

Description of Physical Demands

• Responsibilities may require working outside of “normal” hours, in order to meet business demands.
• The size of the Nordics will necessitate appropriate management of travel requirements to ensure coverage of customers.

Jazz Pharmaceuticals is an Equal Opportunity Employer.

Research scientist

Apply here

About the job

Research Scientist, Research and Development

Are you interested in producing new sustainable food ingredients with one of Europe’s hottest start-up companies? Would you like do impactful work to produce animal free egg white proteins with cutting edge technology with superb colleagues who are top experts in their field? Onego Bio might be just the place for you.

Onego Bio Ltd is a Finnish biotechnology company developing animal-free products such as egg white proteins. The company, founded in 2022, is a VTT spin-off that salutes the remarkable work done by VTT Biotechnology to create next level cell agriculture products and applications. Onego Bio has raised 10 million Euros in seed funding to commercialize a breakthrough technology to produce egg white without chickens. The Onego Bio Ltd shareholders include venture capital investors such as Agronomics and Maki VC. Get to know us better by exploring our webpage www.onego.bio

We are now looking for an experienced research scientist to join our R&D team.

In this position, you will play an essential role in developing, planning, and carrying out research projects with a project team and contribute towards our greater goal of providing animal free egg protein ingredients to the world. Ultimately, we aim to be part of building a sustainable food system with the help of our partners throughout the world. Towards this goal our R&D team will create microbial production systems for expressing egg white proteins using filamentous fungi.

Read more about our past work on the topic:

• https://www.vttresearch.com/en/news-and-ideas/finnish-startup-onego-bio-ltd-raises-eur-10-million-seed-funding-commercialize
• https://www.vttresearch.com/en/news-and-ideas/vtts-technology-production-egg-white-protein-without-chickens-awarded-earto
• https://www.eu-startups.com/2022/03/10-fantastic-fast-growing-finnish-startups-to-watch-in-2022/

Your responsibilities as Research Scientist:

• Scientific project work in the fields of protein production and fungal biology
• Using your expertise in molecular biology and strain engineering to create excellent fungal production strains for egg white proteins
• Developing strain screening technologies and workflows for filamentous fungi
• Further developing our fungal expression platforms using the newest innovations
• Working with our bioprocess team to improve the strains and bioprocess conditions

Who we are looking for:

• Proven, excellent laboratory skills and experience in molecular biology techniques such as DNA cloning, genome engineering, protein analysis, protein purification, and possibly genome analysis
• Completed MSc or PhD in biotechnology, molecular biology, or related field.
• One year or more of experience working with filamentous fungi, or possibly yeast.
• Good scientific reporting skills
• Good written and spoken English skills
• Industrial experience working in a biotechnology company would be a big plus

As a person, we hope that you:

• Skilfully and precisely plan and perform experiments
• Self-motivated and willing to take the initiative to get projects accomplished
• Have strong communication and collaboration skills
• Work well with other team members and contribute to a good working environment
• Can tolerate pressure and maintain a good work-life balance
• Are flexible to take on a variety of tasks anticipated in a start-up company

With Onego Bio, you’ll enjoy: / What we offer you:

• Molecular biology with an impact. Onego Bio works on creating cutting-edge microbial protein production systems. Microbial production technology to produce chicken ovalbumin could mitigate the environmental impacts of chicken-egg-derived ovalbumin according to recent study published in Nature Food (https://www.nature.com/articles/s43016-021-00418-2)
• Superb colleagues. With Onego Bio, you’ll join a small, focused group of top experts who foster a culture of trust, openness and sharing ideas.
• Competitive salary. We want to attract the best people, so we will provide competitive salaries.
• Nordic work–life balance. Working in Finland, the happiest country in the world, enables a great quality of life. At Onego Bio, we make our people’s well-being a priority. We offer 6 weeks paid vacation a year and occupational healthcare.

Apply now and join our community of brilliant minds!

Please send your CV and application letter as soon as possible but at the latest by 30 April 2022. We will process applications as they come in and fill the position as soon as we find the right candidate.

Interested and want to hear more?

For further information, please contact Chris Landowski, Chief Technology Officer, chris@onego.bio

We look forward to hearing from you!

Apply between 12 April 2022 and 30 April 2022 23:59 (Europe/Helsinki)

Employment type: Full-time, Permanent

Location: Helsinki, Finland

Scientist

Hakulinkki

Biovian Oy on vakiintunut turkulainen uuden sukupolven bioteknologiayritys, joka on erikoistunut bioteknologisten lääkeaineiden ja aseptisten lääkevalmisteiden sopimusvalmistukseen ja -analysointiin sekä prosessikehitykseen. Biovianin laboratorio- ja tuotantotilat sijaitsevat Kupittaalla Biocityssä ja Pharmacityssä. Monilla palkinnoilla huomioitu yritys toimii bioalan ytimessä, hyödyntäen modernia biotekniikkaa tuotteissaan ja palveluissaan. Biovian on investoinut uusiin teknologioihin, on tärkeä työllistäjä alalla ja on kasvattanut tasaisesti liikevaihtoaan, josta suurin osa (80 %) tulee viennistä. Lisätietoa yrityksestä www.biovian.com.

Haemme Scientistiä soluviljelyyn

Yhtiön kasvaessa haemme henkilöä Scientist tehtävään soluviljelyyn tuotantotiimiimme. Tutkijan tehtävässä työskentelet sekä käytännönläheisesti soluviljelyn parissa että dokumentoinnin ja raportoinnin parissa.

Tehtäviisi kuuluu asiakasprojekteihimme tehtävä soluviljelytyö sekä työhön liittyvä materiaalihallinta ja dokumentointi. Solupankkitoiminnan työvaiheita ovat asiakasprojektin solupankin prosessin suunnittelu, solupankin materiaalien käytön suunnittelu ja materiaalin hallinta, soluviljely tuotannossa puhdastiloissa, soluviljelyprosessit prosessikehityslaboratoriossa sekä tarvittavan laitteiston hallinta. Tehtäviisi kuuluu myös raportointi, dokumentointi, dokumenttien tarkastaminen ja työohjeiden laatiminen. Raportoit asiakasprojekteille solupankkitoiminnan tuloksista ja laadit ja päivität työohjeita. Toimit tehtävässä kokeneen Scientistin työparina, joka myös perehdyttää sinut työhön.

Job requirements

Odotamme / toivomme sinulta:

Odotamme sinulta kokemusta nisäkässolujen soluviljelystä. Sinulla on soveltuva ammatillinen tutkinto (esim. biologiasta, biokemiasta, farmasiasta tai vastaavasta) sekä käytännön kokemusta laboratorio- tai tuotantoympäristöstä.

Toivomme sinulta

• Kokemusta lääketeollisuudesta
• Kokemusta GMP ympäristössä työskentelystä
• Kokemusta puhdastiloista.

Olet työskentelytyyliltäsi tarkka, järjestelmällinen, reipas ja toimelias henkilö. Sinulla on kyky reagoida muuttuviin tilanteisiin ja erinomaiset vuorovaikutus- ja ryhmätyötaidot.

Sinulla on hyvä suomen kielen taito. Työohjeet ja dokumentointi tehdään englanniksi, joten toivomme sinulta myös hyvää englannin kielen taitoa.

Tarjoamme sinulle:

Tarjoamme merkityksellisen työn, mielenkiintoisia ja monipuolisia työtehtäviä solupankkien parissa sekä hyvän perehdytyksen työhön.

Saat viihtyisän työpaikan, jossa työntekijöitä arvostetaan sekä hyvät henkilöstöedut – tarjoamme työntekijöillemme esimerkiksi laajan työterveyshuollon, terveysvakuutuksen sekä hyvinvointi- ja liikuntaedun.

Työtehtävä on kokoaikainen ja vakituinen ja työtä tehdään pääosin Turussa Kupittaalla, jossa toimipisteemme sijaitsee. Jatkossa sinun on mahdollista työskennellä myös etänä, toivomme kuitenkin, että olet paikan päällä noin neljä päivää viikosta.

Kiinnostuitko?

Täytä hakemuslomake palkkatoiveineen ja liitä mukaan hakemuksesi sekä CV:si 24.4.2022 mennessä.