16.10.2022 | Avoimet työpaikat
Organon
Apply here
Organon is a Women’s Health Company that believes in a better and healthier every day for every woman! We are a passionate, global community of thousands dedicated to redefining the future of women’s health. Our mission is to deliver impactful medicines and solutions for a healthier every day. But what really makes it work at Organon is our people.
We’re looking for real, passionate team players, curious innovators, forward thinkers, empowered by the idea of shaping their career, and ready to bring their fire to embrace change and the opportunities it brings for progress.
At Organon, you’ll get to enjoy the best of both worlds: the open, agile, collaborative culture of a start-up, and operating at the scale of a fortune 500 company with an international footprint that serves people in more than 140 markets.
It’s going to be an exciting future—come be a part of it!
Organon is hiring a Research Senior Scientist to join our team in Turku, Finland.
Purpose of the role
- Independently coordinate basic research activities
- Assist drug discovery lead and senior scientists in drug discovery and development projects
- Assist in establishing priorities and timelines to meet project objectives
- Liaise with both internal cross-functional team members and outsourced partners
The primary responsibilities include but are not limited to the following:
- Coordination of compound logistics and in vitro screening routines
- Coordinating outsourced research activities
- Procuring catalog chemicals, commercial screening compounds and custom synthesis products
- Providing documentation for vendors, couriers, customs, and financial management
- Keeping chemistry database (SAR) up to date, and troubleshooting problems with these databases
- Attending lab meetings, project meetings, and meeting with external collaborators
- Assist project team with preparation of reports and presentations
- Under general guidance
- interpret and evaluate scientific data and screening results
- propose conclusions and follow-up experiments
- review literature and patents
- participate in synthetic route scouting, designing of molecules, SAR analysis
Background Requirements and Qualifications
Required Experience:
- Job experience in the pharmaceutical or biotech industry or in an academic setting is preferred
- General knowledge of synthetic chemistry, common purification techniques, and structure elucidation of organic molecules
- General understanding of drug discovery, medicinal chemistry, and biological principles
- Excellent computer skills and ability to quickly learn and master computer programs, databases, and scientific applications
Position Qualifications:
- MS in organic chemistry, medicinal chemistry, biochemistry, pharmaceutical sciences, or related field
- BSc in organic chemistry, chemical engineering, pharmacy, or related field with 1-5 years of relevant work experience
Required Skills:
- Demonstrated ability to accurately complete detailed work
- Ability to work under deadlines with general guidance
- Strong organizational, teamwork, and problem-solving skills
- Strong verbal and written communication skills in English
- Ability to work effectively with other scientists (chemists, biologists, pharmacologists, etc.) on a complex research project
Who We Are:
Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women’s Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions. Our Vision is clear: A better and healthier every day for every woman.
16.10.2022 | Avoimet työpaikat
FinVector
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As our growth continues, we are now looking for BUFFER PREPARATION SPECIALIST to join our Manufacturing team.
Buffer Preparation is one of the four Manufacturing Streams. Buffer Prep. team produces solutions used in our biological production process. Your main responsibilities as a Specialist include writing and reviewing the documentation of GMP operations. The focus of documentation is on batch record reviews, SOPs, deviations, change controls and CAPAs. Furthermore, you will be (occasionally) performing manufacturing operations in cleanroom environment according to GMP guidelines. You will also be the contact person for the production operators in situations that require problem solving.
It is an advantage if you already have some experience of GMP work and/or you have knowledge of quality systems.
You could be the person, if…
- You produce clear, easily understandable and accurate documentation in English.
- Your working style is precise and you achieve objectives set to you in a timely manner.
- You want to develop yourself and become an expert in your own field.
In order to succeed, you would need a degree in chemistry, biochemistry, biotechnology or any other related field of study. As a person, we would like you to be open-minded towards new challenges and spread good team spirit. All our documentation is in English and the team is international, hence you need to communicate fluently both in written and spoken English. Also earlier experience with project management responsibilities, or similar, is considered as an advantage.
We offer you an active and lively work community, with highly skilled and experienced personnel, in gene therapy manufacturing. Working with us, you are entitled to good employment benefits, such as extensive occupational health-care, and we support your physical and cultural free-time activities. We provide you with a wide initial training and a warm welcome. FinVector is located in vibrant Kuopio, which offers a safe living environment, friendly atmosphere and clean nature.
Our Manufacturing team is working in shifts. We would like you to start preferably in December or January.
Apply by 30th October!
For more information contact Team Lead Saija Callan tel. 044 430 4646 on weekdays between 10-14.
Apply between 10 October 2022 and 30 October 2022 23:59 (Europe/Helsinki)
What we are looking for
- suitable educational background and professional profile
- English skills
Benefits
- ePassi wellbeing benefit
- extensive occupational health-care
- physical and cultural free-time activities
FinVector
FinVector Oy is a growing pharmaceutical company authorized by FIMEA, following the procedure of Good Manufacturing Practice (GMP). FinVector is internationally recognized and is a pioneer in its operational field. FinVector works on the cutting-edge biopharmaceuticals and we’ve invested into building state-of-the-art development and GMP facilities for Viral Vector and Cell Therapy platforms including vaccines. Our research and development agenda is focused on the most commonly used gene therapy vectors: adenoviral, adeno-associated viral (AAV) and lentiviral vectors and innovative cell therapies. FinVector offers a versatile and responsible work environment and the work is done together with a group of professionals from various fields. FinVector is owned by Ferring Ventures and we are located in Kuopio, Finland.
16.10.2022 | Avoimet työpaikat
Invenia Group
Apply here
Do you have significant experience working with NGS-based technologies? Are you open to exploring a new career opportunity?
Invenia Group has partnered with an innovative start-up company specializing in cancer diagnostics. The company provides a dynamic, international, and fast-paced working environment and as part of its rapid expansion plan, we are currently looking for a Field Application Scientist based anywhere in Europe to join the team.
Role responsibilities:
If successful, you will provide technical support and training to customers on-site across Europe. You will work independently from your home office, where you will be responsible for training the commercial teams and working together with the R&D teams to constantly improve the company’s solutions – gathering industry feedback and reporting back internally.
What we are looking for:
We are looking for someone who is creative and has a work-hard-play-hard mindset. Given the technical nature of the role, we are looking for someone with significant experience working with NGS-based technologies, as well as experience with wet lab. A strong background in genetics/molecular biology/genomics is also necessary for this role.
This is a field-based role within Europe, therefore it is suitable for individuals who are highly active with a can-do mindset and happy to spend over 50% of their time traveling across Europe. Fluency in English and any other European language is also a must for this role.
This is a fantastic opportunity to join a company with a great culture, that values work-life balance. Here, you will join a team of experts that value your personal development and make sure that you grow in an environment where you are allowed to learn from your mistakes and improve.
If you are a self-motivated individual with the right background in NGS and are passionate about contributing to the growth of an organisation, then this opportunity could be for you. To find out more information, please apply.
16.10.2022 | Avoimet työpaikat
https://www.linkedin.com/jobs/view/3306122315
About the job
Post-doc researcher for a 2-year position in advanced nanocellulose characterization in Finland
Who are you?
• PhD to be completed soon or completed no longer than four years ago
• Proven track record of using of one of following methods: QCM-D, MP-SPR, AFM
• Fluent in written and spoken English. Finnish is seen as a benefit.
Request full information by e-mail from kari (dot) luukko@upm.com
Send CV and cover letter by October 17th 2022
16.10.2022 | Avoimet työpaikat
https://ats.talentadore.com/apply/paallikko-biopankki/D4goPZ
Haku alkaa 11. lokakuuta 2022 ja päättyy 27. lokakuuta 2022, klo 23.59 (Europe/Helsinki)
Liity auttamisen ketjuun! Haemme Veripalvelun biopankkitoiminnoille ja näytepalvelulle päällikköä.
Biopankkitoiminnan kehittäminen ja tutkimus- ja kehitystoiminnassa tarvittavien näytteiden saatavuuden parantaminen ovat osa Veripalvelun strategiaa. Avaamme uusia tutkimusmahdollisuuksia Veripalvelun biopankin terveiden henkilöiden näytteiden ja tiedon avulla.
Suomessa toimii tällä hetkellä kymmenen biopankkia, joista kaksi toimii Veripalvelussa: Hematologinen biopankki, jonka omistavat Helsingin yliopisto, Suomen Hematologiyhdistys ja Veripalvelu, sekä Veripalvelun Biopankki, joka on erikoistunut verensiirtolääketieteen erityiskysymyksiin sekä luovuttajan että potilaan näkökulmasta. Veripalvelun biopankissa on 55 000 jäsentä ja sen erityispiirteenä on yli 40 000 biopankkisuostumuksen antanutta verenluovuttajaa, joiden antamista näytteistä genomitason variaatio ja HLA-alleelit on määritetty. Säännöllisesti luovuttavilta verenluovuttajilta pyydetään myös lupaa toistuvien näytteiden, muun muassa elävien pakastettujen verisolujen keräämiseen. Näitä tietoja ja näytteitä käytetään suostumusten mukaisesti sekä Veripalvelun johtamissa että muissa merkittävissä tutkimusprojekteissa.
Biopankit ovat biolääketieteellistä tutkimusta tukevia alustoja, joihin kerätään biopankkisuostumuksen antaneiden henkilöiden näytteitä ja tietoja tulevaa tutkimusta varten. Biopankit toimivat biopankkilain säädösten mukaisesti ja ovat viranomaisvalvonnan alaisia.
Tehtäväsi
Keskeisiä tehtäviäsi ovat:
- Kehität biopankkitoimintaa ja tutkimus- sekä tuotekehitysnäytteiden käsittelyä Veripalvelun strategian ja biopankkilain sekä muun lainsäädännön mukaisesti
- Vastaat toimintasuunnitelmasta ja talousarviosta
- Toimit Biopankki ja näytepalvelutoiminnon henkilöstön esihenkilönä
- Vastaat Veripalvelun biopankin kehittämisestä ja toiminnasta lainsäädännön mukaisena vastuuhenkilönä
- Osallistut Hematologisen biopankin johtoryhmätoimintaan ja vastaan operatiivisesta toiminnasta Veripalvelussa
- Huolehdit näyte- ja aineistopyyntöjen käsittelystä ja asiakasprosessien kehittämisestä
- Huolehdit säilytettävien näytteiden laadunvalvonnasta, rekisterien ja tietokantojen ylläpitämisestä, yhdistämisestä ja suojaamisesta
- Kehität tutkimus- ja kehitystoiminnassa tarvittavien näytteiden tarjontaa
- Osallistut sidosryhmäyhteistyöhön.
Teet työtäsi yhdessä osaavan tiimisi kanssa. Raportoit laadunhallinta, tutkimus- ja tuotekehitys vastuualueen johtajalle.
Tehtävä on toistaiseksi voimassa oleva ja aloitus tapahtuu sopimuksen mukaisesti, kuitenkin viimeistään maaliskuussa 2023.
Osaamisesi
Odotamme hakijalta tehtävään soveltuvaa ylempää korkeakoulututkintoa, sekä valmiuksia ohjata ja kehittää biopankkitoimintaa. Edellytämme kokemusta biopankkitoiminnasta ja toiminnasta viranomaisten säätelemässä toimintaympäristössä. Arvostamme soveltuvaa tohtorintutkintoa sekä kiinnostusta isojen tietomäärien käsittelyyn, kokemusta tutkimustoiminnasta ja tutkimusrahoituksen sekä kansainvälisen biopankkitoimintaympäristön tuntemusta.
Tehtävän hoitaminen vaatii hyviä vuorovaikutustaitoja, monipuolisia teknisiä valmiuksia ja vahvaa englannin kielen taitoa. Aiempi kokemus esihenkilötyöstä katsotaan eduksesi.
Tarjoamme
Tarjoamme mielenkiintoisen ja merkityksellisen työn innostavassa ja osaavassa työyhteisössä. Olet osa ainutlaatuista auttamisen ketjuamme vapaaehtoisten luovuttajien sekä terveydenhuollon henkilökunnan kanssa.
Työntekijöidemme hyvinvointi on meille erityisen tärkeää: panostamme muun muassa esihenkilötyön kehittämiseen sekä henkilöstömme jaksamisen tukemiseen esimerkiksi tarjoamalla monenlaisia liikunta- ja hyvinvointietuja. Kattava perehdytys sekä esihenkilösi ja tiimisi tuki auttavat sinua pääsemään työssäsi alkuun ja kehittymään omassa tehtävässäsi. Meille on tärkeää, että jokaisella Veripalvelussa on mahdollisuus osallistua ja vaikuttaa toimintamme jatkuvaan parantamiseen. Lue lisää Veripalvelusta työpaikkana täältä.
Lisätietoja tehtävästä antaa tutkimusjohtaja Jukka Partanen, jukka.partanen@veripalvelu.fi (puh. 050-3707383) ja Kari Aranko, johtaja, laadunhallinta, tutkimus ja tuotekehitys, kari.aranko@veripalvelu.fi (puh 0400-602429). Hae tehtävää viimeistään 27.10.2022 hakulomakkeemme kautta. Käymme hakemuksia läpi jo hakuaikana.
Tarjoamme
- Kulttuuri-, liikunta-, hyvinvointi- ja työmatkaetu (Epassi)
- Laajennettu työterveyshuolto
- Lounasetu
- Työmatkaliikunnan kannustinraha
- Työsuhdepyöräetu
- Pitkät lomat
- Kuntosali ja ohjattuja ryhmäliikuntatunteja omissa tiloissamme Vehkalassa
Suomen Punainen Risti, Veripalvelu
Suomen Punaisen Ristin Veripalvelu tuottaa sairaaloille potilaiden hoidossa tarvittavia turvallisia ja tehokkaita verivalmisteita sekä laboratoriopalveluja. Huolehdimme veren keräämisestä vapaaehtoisilta verenluovuttajilta potilashoidon tarpeiden mukaisesti. Tarjoamme sairaaloille myös kantasolujen ja elinten siirtoja tukevia palveluja. Harjoitamme osaamiseemme liittyvää palvelu-, tutkimus- ja kehittämistoimintaa ja osallistumme biopankkitoimintaan.
Veripalvelu on voittoa tavoittelematon organisaatio. Vuosibudjettimme on noin 60 milj. euroa ja palveluksessamme on noin 500 henkilöä.
16.10.2022 | Avoimet työpaikat
https://www.linkedin.com/jobs/view/3303476509
We are hiring!
Misvik Biology Oy is looking for an enthusiastic research scientist or postdoc to join our toxicology projects. We are involved in European Commission funded Horizon 2020 projects SABYDOMA (https://www.sabydoma.eu/), NanoSolveIT (https://nanosolveit.eu/), HARMLESS (https://www.harmless-project.eu/) and PrecisionTox (https://precisiontox.org/) in which we carry out cell-line-based toxicity assessment utilizing high throughput screening and high content imaging approaches as well as omics analysis.
We are looking for someone who has a background in cell culture work, imaging, data analysis and scientific writing. The work will include (covid permitting) travelling to project meetings.
You would mainly be involved in the PrecisionTox project where our role is to screen 250 human lymphoblast cell lines for toxicity and gene expression differences caused by genetic variability of the cell lines as well as evaluation of causal links between biomarkers and toxic effects predictive of adversity utilising siRNA technology. Most, if not all, of the assays will be carried out in 384-well plate format, so experience using them would be beneficial.
Misvik Biology is a small contract research organization established in 2014 and is based in Turku Finland. Due to our small size, we can offer you great flexibility, competitive salary, and involvement in all aspects of making good science. We are looking for someone who can start in February 2023, at the latest, and stay with us for 3 years. The position will come with a six-month trial period.
Please send your application with a salary request to hongisto@misvik.com.
16.10.2022 | Avoimet työpaikat
https://www.linkedin.com/jobs/view/3309602217
About the job
The University of Oulu is part of the international scientific community producing new scientific knowledge and science-based solutions related to problems of society. The University of Oulu is committed to educate future pioneers for building a more sustainable, intelligent and humane world. Creating new knowledge, taking responsibility, and succeeding together are values that build a strong foundation for all our actions. We offer a working environment where individuals can cultivate their skills, do meaningful work, and develop professionally. The specialized research and service units of the University of Oulu enable extensive and diverse development and career opportunities for experts in various fields. Doctoral researchers in the University of Oulu are part of an international, multidisciplinary scientific community. Doctoral training is coordinated by the University of Oulu Graduate School (UniOGS).University of Oulu has allocated twenty (20) 4-year doctoral researcher positions to the emerging research themes in association with the four focus institutes , , and . The Emerging projects in the strategic focus areas will connect multidisciplinary research across disciplines with the spearhead projects of the University of Oulu.We are now looking for aDoctoral Researcherfor a maximum of four years, starting at the earliest on 01.01.2023 in a research project of Docent/Adjunct Professor Pirjo Åström in the Research Unit of Biomedicine, Faculty of Medicine. The applied position is under the Emerging projects programme 2023-2026 within the context of , which offers a high-level international multidisciplinary environment supplied with cutting-edge infrastructures in the strategic focus areaOur research aims to identify novel mechanisms of immunological disorders. We work in close collaboration with expert clinicians at the Oulu University Hospital and utilize unique, genetically isolated Finnish population to identify novel gene variants leading to dysfunctional immunity. Some gene variants make the individual more prone to infections and may lead to devastating conditions such as viral encephalitis. Such patients, with novel gene variants, provide us with invaluable hints for the biological mechanisms involved in the disease process. In our research, we use human tissue samples and versatile in vitro methodology to study the function of immune system.RequirementsThe position is supervised by Dr. Pirjo Åström and the project’s focus is on identifying novel defense mechanisms of central nervous system (CNS) in viral infection. Eventually, we hope to provide targets for development of novel treatment modalities. Knowledge on neuroimmunology is essential to be prepared for current and future viral threats. Moreover, as neuroinflammation plays a role in various CNS disorders, we may identify mechanisms that, in addition to viral encephalitis, apply for other diseases as well. More information about our research is found on principal investigator’s researcher profile:You must hold a Master’s degree or an equivalent degree (e.g. licentiate) preferably in biochemistry, biotechnology, molecular biology, microbiology, or medicine (or equivalent). We are looking for highly motivated candidate with strong interest in molecular biology and disease mechanisms. A successful candidate has good communication and interpersonal skills. Previous experience in hands-on molecular biology laboratory work and research on immunology is a plus. Degree must have been completed with good grades (at least 60% of maximum grade, or 3/5, in both the taught studies and the Master’s thesis). Ability to pursue independent research and excellent writing and fluency in English is expected.The doctoral researcher position is intended for an Early Stage Researcher (ESR) who, according to the ”European Charter for Researchers and the Code of Conduct for the Recruitment of Researchers”, is defined as a researcher in the first four years (full-time equivalent) of their research activity, including the period of research training. Applicants will either be starting their doctoral training or have completed no more than two full years of training (adjusted for possible previous part-time status) at the time the position is filled. You will carry out your doctoral studies in theWhat We Offer
- We offer you a place in a highly talented research group, working to solve globally significant research problems in the field of immunology.
- University´s wide variety of support services are at your disposal, allowing you to focus on your studies and research.
- In addition to modern research facilities, we offer you personnel benefits such as free occupational healthcare, support for sport services and endless opportunities to develop your skills and competences.
- Regular salary is paid 12 months per year, including paid leave and an additional holiday bonus in the summer.
- The employed person will be insured by the university and provided occupational healthcare. The Finnish government provides benefits to residents and their families, for example possibility to the national healthcare system and high-quality affordable childcare and school services.
Salary and key termsThe salary of selected doctoral researchers will be initially set on level 2, and later on levels 2 – 4 of the national salary scale for the teaching and research staff of Finnish universities. In addition, a supplementary remuneration is given for personal achievement and performance (max. 50 %). In practice, the salary is roughly 2200 – 2700 € (before taxes) per month for an early-stage researcher, depending on the appointee’s qualifications and progress of the doctoral thesis.The positions are fixed term for maximum of four years starting earliest on 1 st of January 2023. A trial period of 6 months is applied to the position.How To ApplyApplications must be submitted through the online system by 6 November 2022, 23:59 (Finnish local time), with the following attachments as three separate pdf files (please note that the online system has a maximum size limit of attachments):
- Complete CV containing contact information of at least two referees and a list of journal and conference publications (if any). A recommended CV template can be found on the webpage of Finnish Advisory Board on Research Integrity (
- Motivation letter describing prior knowledge, research interests and career plans (1-2 pages)
- Certificates/Diplomas: Scanned electronic copies of diplomas and transcripts of the records of relevant previous degrees (MSc and BSc or equivalent). If the original documents are not in English, Finnish or Swedish, each document must be accompanied by an official certified translation into English or Finnish.
Applications sent by email will not be considered.The eligible applicants fitting best in the research profile expected for the position may be invited to an on-site or remote interview. All applicants will be notified when the selection process is completed.For further information
- Docent/Adjunct Professor Pirjo Åström, e-mail: pirjo.astrom
About Oulu, FinlandFinland is one of the most livable countries in the world, with a high quality of life, safety, excellent education system, and competitive economy. The Oulu region is home to over 200 000 people making it the largest urban centre in the Nordics and one of the fastest growing regions in northern Finland. Oulu is a combination of beautiful, northern nature, vivid cultural life and modern technology. Oulu is also known for its highly-educated people and friendly, easy-going atmosphere. Living in Oulu is easy – everything is only max. 20 minutes away! Find out more about Oulu:
16.10.2022 | Avoimet työpaikat
https://www.linkedin.com/jobs/view/3309291432
About the job
I am looking for a Doctoral Researcher for a maximum of four years, starting at the earliest on 01.01.2023. The applied position is under the Emerging projects programme 2023-2026 within Biocenter Oulu, which offers a high-level international multidisciplinary environment supplied with cutting-edge infrastructures for biomedical research.
About the project: Healthy cartilage functions in an environment with low oxygen levels (normoxia) and changes in oxygen sensing have been associated with osteoarthritis. This project aims to clarify hypoxia signaling in cartilage with varying mechanical loading and oxygen pressures. Ultimately our research aims to identify potential therapeutic molecules that can prevent cartilage degeneration and osteoarthritis.
Requirements: You must hold a Master’s degree or an equivalent degree (e.g. licentiate) preferably in biomedical engineering, biotechnology, mechanical engineering or medical/biomedical physics. In this project, it would be beneficial to have some of the following skills:
- Biomechanical testing of tissues
- Tissue and cell cultures
- Sample processing for histology and other methods for tissue composition
- Gene expression analysis
- Microscopy (polarized, confocal, x-ray microscopy) and quantitative image analysis
I am open to candidates with various backgrounds. Please describe in your motivation letter what skills you have and what you would need or like to learn during doctoral studies.
What is Offered
- You will be placed in a highly talented research group, working to solve globally significant research problems in the field of Orthopaedic Research.
- In addition to modern research facilities, we offer you personnel benefits such as free occupational healthcare, support for sports services, and endless opportunities to develop your skills and competences.
- Regular salary is paid 12 months per year, including paid leave and an additional holiday bonus in the summer.
- The employed person will be insured by the university and provided occupational healthcare. The Finnish government provides benefits to residents and their families, for example, the possibility to the national healthcare system and high-quality affordable childcare and school services.
Salary and key terms: Salary is roughly 2200 – 2700 € (before taxes) per month for an early-stage researcher, depending on the appointee’s qualifications and progress of the doctoral thesis. The positions are fixed term for a maximum of four years starting earliest on 1 st of January 2023. A trial period of 6 months is applied to the position.
How To Apply: Applications must be submitted through the online system (Saima) by 6 November 2022, 23:59 (Finnish local time), with the following attachments as three separate pdf files (please note that the online system has a maximum size limit of attachments):
- Complete CV containing contact information of at least two referees and a list of journal and conference publications (if any).
- Motivation letter describing prior knowledge, research interests, and career plans.
- Certificates/Diplomas: Scanned electronic copies of diplomas and transcripts of the records of relevant previous degrees (MSc and BSc or equivalent).
Applications sent by email will not be considered. The eligible applicants fitting best in the research profile expected for the position may be invited to an on-site or remote interview. All applicants will be notified when the selection process is completed.
16.10.2022 | Avoimet työpaikat
https://www.linkedin.com/jobs/view/3314043748
About the job
For further expansion of our Research and Discovery teams, we are now seeking a motivated Technical Scientist with extensive and broad experience in antibody discovery and engineering. Industry research and immunology experience is a plus.
As a technical expert you will be working with project teams and other colleagues to discover and develop therapeutic antibodies. You will use your knowledge, network contacts and literature to scout, evaluate and translate into practice technical and technological opportunities to keep argenx in the forefront of antibody discovery and engineering.
You should be able to work independently and guide the day to day responsibilities of others, helping research associates and other colleagues on the work floor. Candidate must have good communication skills in English – our corporate language – and should be able to work well in a team.
Profile
- Bachelor, master’s degree or PhD who have a long standing and deep research experience in antibody discovery, screening, and/or protein engineering. Industry research and immunology experience are a plus
- Demonstrated hands-on experience with antibody display techniques (e.g. phage display), screening, characterization and engineering of lead antibodies
- Motivated to work in the laboratory, provide support and training across the majority of experimental procedures within argenx
- Quality conscious attitude
- Proactive and creative mind to solve scientific problems
- Excellent team player with focused attitude
- Able to operate in a dynamic surrounding of a fast growing biotech company with challenging timelines
- Fluent in English – our working language
Offer
- A competitive salary package with extensive benefits
- Involvement in discovery and preclinical development of therapeutic antibodies
- A work environment in a human-sized, dynamic biotech company
16.10.2022 | Avoimet työpaikat
https://www.linkedin.com/jobs/view/3231288449
Description
Senior Qualified Person for Pharmacovigilance (QPPV) Office Specialist with Medical Device expertise needed
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.
Job Responsibilities
- Assist the assigned QPPV team in relation to various tasks, meetings and deliverables in relation to specific allocated projects.
- Provide input to proposals and project budgets.
- Participate in the generation and maintenance of quality documents as needed (Policies, SOPs, Charters, Agreements, etc.) in Syneos or in relation to allocated projects.
- Mentor and train global and local PV and non-PV staff to ensure knowledge sharing and in relation to PV processes and required quality, legislation and compliance.
- Liaise with local Safety officers in allocated projects as needed and where required assume vendor management activities for any outsourced post-marketing services included via Syneos Health in global assigned projects.
- Draft, analyze and help develop safety and pharmacovigilance documents as needed to ensure overall project compliance.
- Maintains continuous knowledge and expertise in GVP requirements for pre- and post-marketing pharmacovigilance to ensure sufficient update- to-date advisory skills.
- Support and guide relevant client members and other project team members to deliver relevant objectives in relation to the SDEA including but not limited to safety training, inspection readiness and PV system set-up and PSMF deliverables.
- Performs other work-related duties as assigned.
- Assigned as primary responsible for delivering the Client PSMF.
- Overall responsible for supporting and coordinating the PSMF including all stages in the built, registration and maintenance of the assigned client’s Pharmacovigilance System Master File(s).
- Draft and finalize all documents associated with the PSMF process and facilitate all review processes and approvals.
- Maintain PSMF Repository for allocated projects.
- Assist the QPPV Office team to ensure delivery and updates to the client’s PSMF. Ad hoc and upon urgent request.
- Act as a quality and compliance specialist in the post approval PV area
- Interact directly with clients to collate information for PSMF.
- Implement the PSMF outlined KPIs in client’s PV systems.
- Perform Maintenance of the PV system in Syneos Health and provide attention to detail with allocated client’s quality documents and processes as they related to the PV Quality system.
- Support in enhancement of the PV Quality system for allocated projects as needed.
- Draft, update, and author PV Corrective and Preventative action (CAPA) plans to ensure correct reflection of open findings and deviations in the PSMF and when needed work on associated changes or updates to the Syneos Health or client procedures whichever apply.
- Can act as lead operational PV CAPA support for clients identified deviations or findings to enhance their PV quality System.
- Lead or support gap analysis of client pharmacovigilance systems.
- Assigned as primary responsible SDEA Specialist to specific projects and is responsible for ensuring that the client SDEAs are in place and the components included in the SDEAs are updated and prepared according to plan, procedures, and legislation to ensure compliance.
- Complete contractual review and manage Client/customer third Party agreements, or draft new or update existing contracts, with respect to pharmacovigilance and the exchange of safety data.
- Arrange meetings to overall coordinate negotiate and finalize the client’s third Party Agreements to ensure finalization and implementation.
- Maintain contractual overview for the assigned clients when relevant in relation to SDEA oversight.
- Participate in internal improvements of the Syneos SDEA processes and SDEA templates covering the post marketing PV system.
- Interact directly with clients, their third parties, including their respective operational teams and legal stakeholders, to collate, update or clarify information for the contracts & agreements including SDEAs as needed.
- Implement the finalized SDEA and train all involved parties responsible for safety activities and timelines outlined in the SDEA.
- Act as contact point for business partners, other departments, third party provider(s), authorities and other partners regarding SDEAs for allocated projects.
- Draft, update, and author PV corrective and preventative action (CAPA) plans when related to the SDEA area or other area as defined in the SDEA template.
- Act as SDEA SME and go-to point of contact for allocated projects.
- Minimal travel may be required (up to 25%).
Qualifications
What we’re looking for
- BA/BSc. in life sciences, Registered Nurse (RN), pharmacist or equivalent combination of education and experience or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills and abilities to perform the job
- Exposure to and knowledge of QPPV related activities
- Very structured and detail-oriented with an excellent ability to keep the overview of complex projects.
- Excellent communication skills including written and verbal communication.
- Excellent understanding of post-marketing safety requirements, ICH GCP, GVP and regulations related to Safety and Pharmacovigilance.
- Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), Visio, email (Outlook), TeamShare (or other management/shared content/workspace), and internet. Basic MS Project skills are preferred.
- Above average attention to detail, accuracy, and organizational, interpersonal, and team-oriented skills.
- Ability to perform several tasks simultaneously to meet deadlines preferred.
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.