Biovian on vahvasti kasvava turkulainen bioteknologiayritys. Tarjoamme sopimusvalmistusta, -analysointia ja prosessikehitystä biotekniikkayrityksille, jotka kehittävät innovatiivisia geeniterapioita tai biofarmaseuttisia tuotteita. Saatamme asiakasprojekteja laboratoriosta kliiniseen potilaskäyttöön asti taidolla, innolla ja sydämellä – tämä on meillä Manufacturing Happiness.
Scientist, microbiology
Yhtiön kasvaessa haemme vahvistusta laadunvalvontaan, mikrobiologisten lääkkeiden analytiikan pariin. Tutkijan työtehtävät ovat monipuolisia laadunvalvonnan tehtäviä, joista keskeisimpiä ovat mikrobiologisten analyysien tarkastus, raportointi ja laboratoriotöiden ohjaus.
Tehtävässä osallistut biologisten lääkkeiden kehitys- ja tuotantoprojekteihin ja pääset rakentamaan modernien lääkkeiden laatua. Lisäksi osallistut analyysimenetelmien kehittämiseen ja validointiin sekä laboratorion laatutason ylläpitoon. Työskentelet asiakasprojekteissa yhdessä Biovianin muiden asiantuntijoiden kanssa. Työ on itsenäistä ja tukenasi on osaava laadunvalvontatiimi.
Job requirements
Työssä onnistuaksesi
Odotamme sinulta tehtävään soveltuva ylempi korkeakoulututkinto (esim. mikrobiologiasta tai biokemiasta). Sinulla on hyvät perustiedot sekä käytännön kokemusta mikrobiologisesta analytiikasta.
Toivomme vahvaa osaamista joillakin alla mainituilla osa-alueilla ja hyvää asiantuntemusta useimmista niistä:
Kokemusta lääketeollisuudesta
Kokemusta GMP-ympäristössä työskentelystä
Raportoinnista ja dokumentoinnista
Olet työskentelytyyliltäsi tarkka, järjestelmällinen, reipas ja toimelias henkilö. Sinulla on vastuunkanto- ja paineensietokykyä. Sinulla on myös hyvät vuorovaikutus- ja ryhmätyötaidot.
Sinulla on hyvä suomen kielen taito ja pystyt työskentelemään sujuvasti sekä kirjallisesti että suullisesti myös englannin kielellä.
Mitä sinä saat meiltä?
Tarjoamme sinulle näköalapaikan biologisten lääkkeiden kehitykseen ja sopimusvalmistukseen sekä monipuolisen työn biologisten lääkkeiden kehityksen kärjessä.
Kattavan perehdytyksen tehtävään ja mahdollisuuden ammatilliseen kehittymiseen.
Viihtyisän työpaikan sekä hyvät henkilöstöedut – tarjoamme työntekijöillemme esimerkiksi laajan työterveyshuollon, terveysvakuutuksen sekä hyvinvointi- ja liikuntaedun.
Työtehtävä on kokoaikainen ja vakituinen. Työtä tehdään Turussa Kupittaalla, jossa toimipisteemme sijaitsee.
Lisätietoja tehtävästä antaa laatujohtaja Marjo Hämäläinen (puh nro 040 706 0874) ja tiimin esihenkilö QC Manager Leena Pitkänen (puh nro 045 678 5827). Marjon tavoitat parhaiten 22.11. klo 14:30-15:30 ja Leenan parhaiten 16.11. klo 15:30-16 ja 28.11. klo 8:30-9:30.
Kiinnostuitko?
Lähetä hakemuksesi palkkatoiveineen viimeistään keskiviikkona 30.11.2022. Käymme hakemuksia läpi hakuaikana ja täytämme tehtävän heti sopivan henkilön löydyttyä.
Tule mukaan työskentelemään kanssamme tulevaisuuden biologisten lääkkeiden parissa ja muuttamaan ideoita tuotteiksi!
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.
The University of Eastern Finland invites applications for a project researcher position at the Institute of Public Health and Clinical Nutrition, Faculty of Health Sciences, Kuopio campus. The positions will be filled for a 2-year term from January 2, 2023 (or as agreed). Please find more information below and submit your applicationno later than November 30, 2022.
Role and salary
The University of Eastern Finland (UEF) is seeking highly motivated applicants for a postdoctoral position in epidemiological analyses of microbial exposures and respiratory health.
As our new project researcher, you will be working at the Institute of Public Health and Clinical Nutrition in a consortium project focusing in identifying early-life microbial exposures affecting asthma risk. The project aims at facilitating the development of asthma preventive interventions. The work builds on our previous findings and existing data from a globally unique compilation of prospectively followed birth cohorts from different countries. Your main role will be to perform statistical analyses, draft manuscripts and drive the harmonization of birth cohort datasets obtained from multiple study centers around the world.
The salary is determined according to the salary system of Finnish universities, and it will depend on the expertise of the recruited applicant and based on either level 5 or 6 on the job requirement chart for teaching and research staff. In addition to the job requirement component, the salary includes a personal performance component, which ranges from 6% to 50% of the job requirement component. With a level 5 job requirement component and the personal performance component, the starting salary will be from 3,350 to 3,900 euros per month. The position is filled for a fixed term as it is tied to a fixed project, but extension may be applicable. A probationary period is applied to all new members of the staff.
Requirements and expectations
Required: The applicant should hold a PhD in a relevant field or an MD and have a strong background in microbiome data analyses, experience in statistical modeling utilizing high quality cohort datasets and have a good understanding of epidemiology. A proven track record of high-quality peer-reviewed publications as a leading author, excellent communication skills and proficiency in verbal and written English is essential. In exceptional cases if other requirements are fulfilled, a candidate with an MSc or equivalent degree may be considered.
Desired: Prior experience in research addressing immunological disorders especially in regard to respiratory and allergic diseases, strong R skills, data illustration and basic understanding of bioinformatics are desired.
Your benefits
You will have an opportunity to work in multi-institutional collaboration with experts in epidemiology, bioinformatics, statistics, data management and national and global collaboration networks. With dedication and enthusiasm, you will have a unique opportunity to address and solve intriguing scientific questions with high public health impact, produce high quality publications and to advance your research career in an innovative environment.
You will have access to the university’s staff benefits, including:
Extensive occupational health care
Staff discount on lunch in our campus restaurants and other services
Enjoy your life in the middle of the beautiful Finnish Lakeland! Finland is known for its cleanliness, welfare know-how, modern technology and superb education system. It is an exotic and safe country to work in. Please visit the Life in Finland section on our website to learn more.
How to apply?
Submit your application using our electronic application form no later than November 30, 2022 (by 24.00 hours Finland time).
Please note that you must include the following appendices in your application
Global Preclinical CRO Seeking Scientists and Senior Scientists with Experience in Ophthalmic Drug Discovery
Experimentica Ltd. is seeking Scientists and Senior Scientists to complement their team at multiple locations, including Kuopio (Finland), Vilnius (Lithuania) and Fort Worth, TX (USA).
We are seeking individuals with proven experience in preclinical biomedical sciences and experience with rodent models for ophthalmic diseases and ocular pharmacology. Candidates will apply their scientific and leadership skills in support of colleagues and projects focused on the discovery of novel therapeutics for ocular diseases. The ideal candidate is someone who is flexible and excited to be a part of a collaborative, fast-paced biotechnology company committed to improving the lives of patients through accelerating the preclinical drug discovery pipelines of our Sponsors.
Responsibilities
In support of our In Vivo Pharmacology teams, develop and execute laboratory work, plans/schedules independently following division/site performance standards and metrics. Techniques may include any or all of the following:
Perform various types of preclinical ocular safety and efficacy studies in preclinical laboratory animal species
Author technical documents, such as study protocols, study reports, and operating procedures
Review technical documents for accuracy, thoroughness, and compliance
Supervise technical staff, including work assignments and performance management
Communicate with customers
All other duties as assigned.
Qualifications
Education: M.S., D.V.M. or Ph.D. in Biology, Molecular Biology, Biochemistry, Neuroscience, Pharmacology or related field
Experience: Masters with 2-4 years of relevant experience preferred, Doctorate Degree with 0-2 years of relevant experience preferred.
Knowledge/Skills Requirements
Maintain high quality laboratory documentation in accordance with applicable regulatory guidance and site SOPs
Develop and execute complex procedures or methods with high quality
Becoming familiar with drug development milestones and their context
Excellent written and verbal communications skills with internal and external customers
Supervisory skills are expected for Scientists with direct reports
Lead by example according to Experimentica’s values and culture
Strategy is focused on personal and team time management and efficiency
Well-organized with ability to multitask
Ability to work effectively under pressure to meet deadlines
Familiarity with safe and efficient laboratory practices
Eagerness to be part of a fast-growing, global Contract Research Organization that helps improve patient lives by accelerating preclinical drug discovery for ocular diseases
About us
Experimentica is a global preclinical contract research organization helping sponsors from pharma, biotech, and academia accelerate their drug discovery and development efforts for ophthalmic disorders with an urgent unmet clinical need. Headquartered in Kuopio, Finland, we support our global client base from laboratories in Fort Worth, TX, DeKalb, IL, Vilnius, Lithuania and our Business Development team in Marseille, France.
Experimentica Ltd. is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. Experimentica Ltd. makes hiring decisions based solely on qualifications, merit, and business needs at the time. For more information, please contact us: info_us@experimentica.com
To apply
Please submit your resume and cover letter to careers@experimentica.com referencing job #22-03.
Two PhD positions are open for enthusiasts of stem cells and cancer metabolism in the recently established Najumudeen Lab at the University of Helsinki.
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.
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.
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.
We are looking for 1-2 motivated Doctoral Researchers who have enthusiasm for the development of protein-based next-generation second-generation vaccine technologies against pandemic pathogens.
Job description
Business Finland, Tampere Tuberculosis Foundation and Finnish Cultural Foundation-funded project PREPARE at the Faculty of Medicine and Health Technology will demonstrate proof-of-concept for the functionality of our protein-based coronavirus vaccine, strongly emphasizing the identification of the optimal route of commercialization for the developed vaccine.
To strengthen our team, we are looking for highly motivated Doctoral Researchers to contribute to the research, proof-of-concept as well as commercialization activities of the developed vaccines. Full-time doctoral studies are expected to be completed in four years.
Requirements
The project is intended for any suitable candidate with MSc degree in the field of molecular cell biology, biotechnology, immunology, protein engineering, process engineering, bioprocess development, immunobiology or any other relevant field connected to vaccine development, vaccine manufacturing or immunology. We value efficiency, perseverance, flexibility, positive team-player attitude, honesty, motivation, and skills to learn new things. In this regard, we greatly appreciate your success in your previous assignments. However, you may be able to convince your suitability to the project with successful application and interview as well.
Extra credits are given if your track record shows experience from the following:
Protein engineering
Recombinant protein production in insect, mammalian and/or bacterial cells
Recombinant protein purification (especially with industrially compatible methods)
Proficiency in working in GLP-/GMP-compliant laboratories
Ability to create and adjust Standard Operating Procedures for the working environment and for the methodology
Quality control analyses for protein-based vaccines
Preclinical mouse work (and qualifications to design and conduct preclinical studies)
Immunological and safety analyses for the vaccine (especially determination of vaccine-specific T-cell immunity)
Applicants are invited to describe their experience of the methods/assignments listed above. Successful applicants may complement each other’s skills. Successful applicants are expected to devote most of their time to research, commercialization activities, publishing and collaboration with other project members and international partners.
Successful candidates must be pursuing or will be accepted to study towards a doctoral degree in the doctoral programme of the discipline. Please visit the admissions webpage https://www.tuni.fi/en/study-with-us/programmes/doctoral-programmes for more information on eligibility requirements.
The work will be done in cooperation with experienced researchers and the ideal candidate must be ready to learn new techniques/methods and continuously develop his/her skills, as well as be able to work in international environment. The work requires good/excellent command of English.
We Offer
The positions will be filled for a fixed-term period of 18 months and successful applicants are expected to apply funding for completion of their doctoral studies from Tampere University graduate school as well as private foundations. We hope the selected candidate(s) can start as soon as possible (earliest 1st of September, 2022) based on mutually agreed start date. A trial period of six months applies to all our new employees.
The salary will be based on both the job requirements and the employee’s personal performance in accordance with the Finnish University Salary System. According to the criteria applied to teaching and research staff, the position of a doctoral researcher is placed on level 2-4 of the job requirements scale. The salary of the Doctoral Researcher follows the university policy. A typical starting salary for a Doctoral Researcher is about 2500 EUR per month. The salary increases based on experience and the progress of doctoral studies.
We offer a wide range of staff benefits, such as occupational health care, flexible working hours, excellent sports facilities on campus and several restaurants and cafés on campus with staff discounts. Please read more about working at Tampere University.
Our team is known for working hard with a humorous attitude, so you are welcome to enjoy our bad jokes, too!
How to apply
Please submit your application through our online recruitment system (link below). The closing date for applications is 31st of August 2022 (at 23.59 EEST / UTC+3). Please write your application and all accompanying documents in English and attach them in PDF format.
Applications should include the following documents:
// The application deadline has been extended to 31st of August 2022 (at 23.59 EEST / UTC+3). //
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Tampereen yliopisto ja Tampereen ammattikorkeakoulu muodostavat yhdessä Suomen toiseksi suurimman monitieteisen, innostavan ja vaikuttavan tutkimus- ja oppimisyhteisön. Korkeakouluyhteisömme osaamiskärjet ovat tekniikka, terveys ja yhteiskunta. Lue lisää: www.tuni.fi
Dosentti Minna Hankaniemen tutkimusryhmä lääketieteen ja terveysteknologian tiedekunnassa etsii 1-2 väitöskirjatutkijaa Business Finlandin Research to Business (R2B) hankkeeseen, jossa pyritään löytämään paras väylä kehitetyn proteiinipohjaisen koronarokoteteknologian kaupallistamiseen. Tutkimusryhmä keskittyy pääasiassa kehittämään toisen sukupolven proteiinipohjaisia rokoteteknologioita pandeemisia taudinaiheuttajia vastaan ja tutkimustyössä huomioidaan tutkimustulosten kaupallistamisen potentiaali ja pyritään rakentamaan tutkimustuloksista uutta liiketoimintaa.
Väitöskirjatutkijalla on oltava tai hänen tulee hakea oikeutta suorittaa tohtorintutkinto Tampereen yliopistossa.
Hakuohjeet
Lue tarkemmat tiedot tehtävästä ja hakuohjeet yllä olevasta englanninkielisestä ilmoituksesta.
Jätäthän hakemuksesi yliopiston sähköisellä hakulomakkeella (linkki löytyy tämän ilmoituksen alta). Hakuaika tehtävään päättyy 31.8.2022 klo 23.59.
// Hakuaikaa on jatkettu 31.8.2022 klo 23:59 asti. //
Innostaisiko sinua työ nopeasti kehittyvällä alalla? Geneettinen analytiikka kehittyy kiihtyvällä vauhdilla ja vaikuttaa yhä useamman potilaan hoitoon. Genetiikan laboratorio tarvitsee lisää ammattilaisia vastaamaan tähän haasteeseen.
HUS Diagnostiikkakeskus on Suomen johtava kliinisten laboratorio- ja kuvantamispalvelujen tuottaja. HUS Diagnostiikkakeskuksen pääasiallinen toiminta-alue on HUS-kuntayhtymän erikoissairaanhoito ja HUSiin kuuluvien kuntien perusterveydenhuolto sekä Kymenlaakson sosiaali- ja terveyspalvelujen kuntayhtymän (Kymsote) ja Etelä-Karjalan sosiaali- ja terveyspiirin (Eksote) alueen laboratorio- ja kuvantamistoiminta. HUS Diagnostiikkakeskuksessa työskentelee noin 3500 laboratorio- ja kuvantamisalan asiantuntijaa ja toimintaa on yli 170 toimipisteessä.
HUS Diagnostiikkakeskuksen Genetiikan laboratorio on nopeasti kasvava diagnostisia genetiikan laboratoriotutkimuksia tarjoava laboratorio. Laboratorion tutkimusvalikoima kattaa laajasti sekä perittyjen että somaattisten muutosten tutkimuksia ja toiminta on voimakkaasti siirtymässä genomin laajuisiin tutkimuksiin. Laboratoriossa voi siten saada monipuolisen ja vahvan koulutuksen ja ammattitaidon sairaalageneetikon tehtäviin.
Haettavana oleva sairaalageneetikon koulutustoimi tähtää asetuksessa (564/94) tarkoitettuun sairaalageneetikon pätevyyteen. Toimi täytetään erikoistumiskoulutuksen edellyttämäksi ajaksi. Liitä hakemukseesi selvitys omasta sairaalageneetikon koulutuksen vaiheestasi (hyväksytyistä kliinisen ja teoreettisen koulutuksen suorituksista tai suunnitelma koulutukseen hakeutumisesta, mikäli et ole vielä koulutusohjelmassa) erillisenä liitteenä.
Tehtävän hoitaminen edellyttää sinulta aloitteellista ja itsenäistä työotetta, hyvää organisointikykyä, hyviä vuorovaikutustaitoja sekä innostusta uuden oppimiseen ja kehittämiseen.
Edellytämme asiakas- ja potilastiloissa työskentelevältä tartuntatautilain pykälien 48 ja 48 a mukaista rokotussuojaa, ja terveydenhuollon toimintayksiköissä työskentelevältä terveydentilan selvitystä keuhkotuberkuloosista.
Yhteystiedot
Lisätietoja tehtävästä antavat ylilääkäri Anna-Kaisa Anttonen, puh. 050 427 0523 ja sairaalageneetikko Kirsi Kiiski, puh. 050 428 7258.
Etsimme uusia osaajia tuotantoomme injektiovalmistukseen Espooseen!
Tehtävän kuvaus
Oletko kiinnostunut työskentelemään merkityksellisen työn parissa Orionin toiminnan keskiössä? Varmuus tuotteidemme ja toimintamme laadusta, luotettavuudesta ja turvallisuudesta on yksi tärkeimmistä toimintamme kulmakivistä. Tule kanssamme rakentamaan hyvinvointia!
Prosessinhoitajana tehtäviisi kuuluu injektioliuosten valmistusta, laitteiden ja välineiden puhdistamista, työvaiheiden kirjaamista sekä laaduntarkkailua. Työ tehdään kirjallisten ohjeiden mukaisesti puhdastilassa steriilituotannon GMP-määräyksiä noudattaen.
Työ on osittain itsenäistä, mutta teet tiivistä yhteistyötä vuoron muiden työntekijöiden kanssa. Välillä voi tulla suunnitelmiin nopeitakin muutoksia ja niihin pyritään reagoimaan joustavasti ja asiakaslähtöisesti. Työ on osittain fyysisesti rasittavaa.
Palkkaamme henkilön vakituiseen, kokoaikaiseen työsuhteeseen. Töitä tehdään keskeytyvässä 2-vuorossa. Työt sijaitsevat hyvien kulkuyhteyksien päässä Espoon Mankkaalla, Urheilupuiston metroaseman lähellä.
Yksikön kuvaus
Injektio-osastolla työskentelee yhteensä n. 50 henkilöä. Osaston päätehtävä on huolehtia injektiotuotteiden valmistuksesta aina liuoksesta pakkaamiseen asti. Valmistuksen jälkeen liuos täytetään pulloihin tai ampulleihin. Jokainen pullo ja ampulli tarkastetaan visuaalisesti ennen kuin ne siirtyvät pakkaamoon, jossa tuotteet pakataan asiakkaille. Lisäksi osastolla on oma pesula ja välinehuolto, missä käytettävät välineet pestään ja steriloidaan.
Tarjoamme sinulle erittäin hyvän perehdytyksen ja koulutuksen tehtävääsi sekä mahdollisuuden kehittyä ja lisätä osaamistasi urasi aikana.
Lisäksi tarjoamme:
kilpailukykyisen kuukausipalkan, joka voi perehtymisen jälkeen kaksivuorotyössä ja tehtävästä riippuen olla jopa 2300–2700 € kuukaudessa. Palkkaan sisältyvät työehtosopimuksen mukaiset vuorolisät sekä työsuoritukseen perustuva tuotantopalkkio.
mahdollisuuden yhtiön tulokseen perustuvaan vuosipalkkioon.
kattavat henkilöstöedut kuten liikunta- ja kulttuurietu, terveys- ja kosmetiikkatuotteiden laajan valikoiman ikiomassa henkilökuntamyymälässämme.
Orionin kuntosali ja erilaisia liikunta- ja harrastekerhoja.
talon sisäisen työterveyspalvelun Espoon toimipisteessämme.
Ihmisten hyvinvoinnin kehittämiseen liittyvä työn merkityksellisyys on avaintekijä siinä, miksi Orionilla viihdytään erinomaisesti. Lue lisää arvoistamme nettisivuiltamme. Tarjoamme sinulle myös mahdollisuuden kehittyä ja lisätä osaamistasi urasi aikana.
Edellytykset
Aikaisempi kokemus erilaisista tuotannon työtehtävistä tai puhdastilatyöskentelystä katsotaan eduksi. Olet oma-aloitteinen ja yhteistyökykyinen sekä luonteeltasi tarkka ja huolellinen. Tehtävissä menestyminen edellyttää hyvää suomen kielen taitoa, sekä valmiutta 2-vuorotyöhön.
Lisätiedot
Mikäli kiinnostuit, niin haethan tehtävään viimeistään keskiviikkona 31.8.2022! Jätäthän hakemuksesi pian, sillä etenemme sopivien hakijoiden kanssa jo hakuajalla. Lisätietoja tehtävästä antaa työnjohtaja Susanna Veini (puh. 050-9663495, ma-pe klo 10-14).
