Hr On Demand Sweden AB jobb

Are you a highly skilled and collaborative in vitro scientist? Would you like to develop assays and run experiments to qualify candidates for our rapidly developing siRNA portfolio? Are you eager to work with super nice colleagues to deliver impactful data and be an integral part in our streamlined organizational structure with short decision routes? If yes, please read further! About usRibocure Pharmaceuticals AB (Ribocure) is an international R&D Centre based at GoCo in Gothenburg, and is a subsidiary of Suzhou Ribo Life Science Co., Ltd. (Ribo). Ribo was established in 2007 in China and is a company with a vertically integrated cutting-edge RNAi technology including patented GalNAc liver-targeting technology -Ribo-GalSTARTM, oligonucleotide design, screen, preclinical proof of concept and clinical testing as well as large scale CMC capacity. Ribocure was established in Jan 2022 in Gothenburg and represents Ribos commitment to globalize its technology and develop life-saving therapies. Ribocure has a Ph2 clinical trial unit and an in vitro lab integrated in our HQ located in GoCo area in Mölndal, Sweden. The clinical trial unit is dedicated to run innovative clinical trials with the focus on rare disease indications to address unmet medical need. (www.ribocure.com) The role We are currently seeking a motivated, skilled and experiencedIn vitro Lab Scientistto help drive the development of our siRNA therapeutics. The scientist will be responsible for conducting advanced cell culture work, including IPS derived cell and organoid models, and molecular analysis of protein and mRNA expression. Experience working with siRNA is highly meriting. Responsibilities: Conduct cell culture experiments (primary, cell lines and pluripotent stem cells) Support in vitro screen in primary cells Set up organoid models to create complex tissue structures in vitro Analyze protein and mRNA expression Maintain accurate records of experiments and data reports Participate in lab meetings, present research findings, and contribute to scientific discussions Keep up-to-date with current literature in the field and implement new techniques and methods as necessary Requirements: PhD or MS in Biology, Biochemistry, or related field A minimum of 2 years experience from Pharma Industry anddrug development Extensive experience with cell culture techniques Experience with IPS derived cell work and organoid models Experience of imaging techniques and analysis Proficiency in molecular analysis of protein and mRNA expression Ability to work independently and as part of a team Excellent communication and organizational skills Attention to detail and ability to maintain accurate records of experiments and findings Ability to multitask and manage multiple projects simultaneously What we offer We offercompetitive salary, comprehensive benefits packageand opportunities for advancement. We are an equal opportunity employer and welcome applicants from all backgrounds. We also offer you opportunities to grow with our fast-expanding global organization towards being one of the leading players in oligonucleotide therapeutics. Come join us at Ribocure and help shape the future of medicine! Send your application by clicking Send Application. Should you have any further questions regarding the position, please do not hesitate contacting Dr Johannes Wikström. Welcome! This recruitment is quality assured by HR On Demand.

We would like to welcome you to a warm yethighly skilled and experienced team ofdrug development professionals focused on oligonucleotide therapeutics. We offer a vibrant collaborative international environment, where science and data are the main driving forces behind our ambition to develop game-changing medicines to our patients. We also offer you the opportunity to grow with our expanding global organization, towards being one of the leading players in the oligonucleotide therapeutics area. About usRibocure Pharmaceuticals AB (Ribocure) is an international R&D Centre based at GoCoin Gothenburg, and is a subsidiary of Suzhou Ribo Life Science Co., Ltd. (Ribo). Ribo was established in 2007 in China and is a company with a vertically integrated cutting-edge RNAi technology including, patent GalNAc liver-targeting technology – Ribo-GalSTARTM, oligonucleotide design, screen, preclinical proof of concept and clinical testing as well as large scale CMC capacity. Ribocure was established in Jan 2022 in Gothenburg and represents Ribos commitment to globalize its technology and life-saving therapies. Ribocure has a Ph2 clinical trial unit integrated in the core business at our HQ located in ourin Gothenburg Sweden and are dedicated to run innovative clinical trials with the focus on rare disease indications to address unmet medical need. (www.ribocure.com) The roleTo further strengthen our global R&D capacity, we are now recruiting a Regulatory Affairs Lead. You will be responsible for providing operational and strategic regulatory leadership to the preclinical and clinical development. With your up-to-date regulatory knowledge, you will contributeto identify future regulatory requirements and proactively drive regulatory interactions to pave the way for innovative clinical development strategies. What you’ll do Provide global regulatory strategy guidance to our pipeline based on up-to-date regulatory knowledge and ensure that they comply with relevant laws and regulations. Responsible for preparation and submission of regulatory agency applications, reports, and correspondence. Prepare and lead interactions with Health Authorities. Represent Regulatory Affairs in cross-functional project teams, to deliver high quality global regulatory strategy documents for assigned products. Communicate regulatory information to multiple departments. Develop and maintain standard operating procedures and local working practices. Lead authoring of regulatory documents. Essential for the role Strategic thinking and influencing toward innovative clinical development approaches through proactive and innovative regulatory strategies. High competencies in oral and written communication skills and have excellent regulatory knowledge including novel regulatory tools and technologies. Academic degree in a science related field. Extensive knowledge of regulatory affairs within one or more therapeutic areas in early and/or late development and FDA and EMA submission. Experience in preparing and/or leading health authority interactions. Demonstrated ability to work collaboratively in a matrix organization. Desirables for the Role Previous experience in oligonucleotide therapies is not a must but strongly preferred. > 5 years of experience from large pharma and/or biotech companies You will be reporting to the Global Head of Regulatory Affairs and the career level will be set based on your experience and competencies. If you are interested, please do apply as soon as possible. For further questions as a candidate for the role,please contact recruiting manager Maria Liljevald. You apply easily by clicking on the Send Application-button no later than April 30th, 2024. Welcome to Ribocure!