2017 KASBP Fall Symposium Job Fair 2017 년 KASBP Fall Symposium 기간중에 Job Fair 가준비되어있습니다. 현재 Job Fair 에참여하는 회사는 ; The following companies are participating in Job Fair during 2017 KASBP Fall Symposium: 대웅제약 Daewoong Pharmaceutical 녹십자 ( 목암생명과학연구소 ) Green Cross & Mokam Life Science Research Center LG 화학생명과학사업본부 LG Chem and Life Science SK 바이오팜 SK Biopharmaceuticals SK Life Science 브릿지바이오 Bridge Biotherapeutics 큐라켐 Curachem 이렇게 7 개회사입니다. 각회사의자세한모집공고는첨부되어있습니다. 한분이여러회사에지원가능합니다. Job Interview 시간은 10/27 금요일오후 3:00 부터 5:30 까지입니다 ( 브릿지바이오는토요일만가능 ). 위시간이여의치않은경우는 KASBP 담당자에게별도의연락으로조정이가능합니다. The interview will be 3-5:30 pm on Friday, 10/27. Bridge bio will be available only for Saturday. For other appointment, please send a request to jobfairkasbp@gmail.com. 지원하고싶은회원께서는각회사들의공고내용을확인하시고, 일차로아래 KASBP 담당자에게해당 회사에서요구하는지원서혹은 CV 를이메일로 10 월 20 일전에보내주시기바랍니다. 회사에직접 보내실경우도아래 KASBP Job Fair 담당자에게보내주셔야인터뷰시간과장소를제공합니다. Please send your CV/application as required in the following posting by each company, by October 20, 2017 to jobfairkasbp@gmail.com for an interview scheduled during the symposium, even though you may apply directly to the company. 제출하신서류를해당회사에서일차로심사한뒤에, 심포지엄현장에서인터뷰가이어질예정입니다. 질문이있으신경우에저희담당자에게연락주시길부탁드립니다. 감사합니다. After reviewing the documents first, there will be an interview during the symposium. Please contact jobfairkasbp@gmail.com for any questions. Thank you KASBP Job Fair 담당자 : 최석태 (Suktae Choi) jobfairkasbp@gmail.com
대웅제약채용공고문 DAEWOONG 대웅제약은 " 삶의질향상을선도하는 Global Healthcare 그룹 " 으로의도약을위해혁신신약등의자체연구개발뿐만아니라오픈콜라보레이션을통한연구개발활동을활발하게진행하고있습니다. 글로벌경쟁력을갖춘 R&D 중심제약회사로거듭나기위해대웅제약연구본부에서함께일한열정적이고실행력을겸비한우수인재를아래와같이모시고자합니다. 직원이성장할수있는모든기회가열려있는곳, 대웅제약에서당신의꿈을이루시기바랍니다. 모집부문 대상분야직무전공우대및필수사항근무지 제제연구 신규플랫폼기술제안및특허출원 데포주 / 패치 / 복합신약등처방및공정연구 신약 fomulation 의약품인허가자료 (CTD 등 ) 작성 약학, 고분자화학및유사전공 약사우대 유기합성 / 의약화학 신약후보물질도출을위한선도물질최적화연구 신규과제기획및과제관리 후보물질대량합성을위한공정연구 신물질및 API 물성, 결정형연구 약학, 의약화학, 유기합성및유사전공 약사, 수의사우대글로벌제약사업무경헙자우대 분자모델링 신약연구를위한분자모델링 (CASS) 업무 구조 - 기반 (SBDD) & 리간드 - 기반 (LBDD) 연구 라이브러리관리, 활용및 Bioinformatics 연구 신약프로그램수행경험우대해당분야박사학위필수 비임상연구 ( 활성 / 약효 /PK/ 독성 ) 신약 / 바이오 / 개량신약활성, 약효, PK, 독성연구및평가생물학, 수의학, 약학및유사전공 약사, 수의사우대글로벌제약사업무경헙자우대 경기용인 바이오분석 분석법개발및검증 cell-based assay 기기분석, 단백질분석 (1 차 / 고차구조및당구조분석 ) 약학, 화학, 생물학및유사전공 CTD 작성경험자우대통계분석전문가우대글로벌제약사업무경험자우대 줄기세포 줄기세포특성분석및기전연구생명과학, 약학및유사전공 박사학위우대글로벌제약사업무경험자우대 바이오의약품 ( 발효공정 / 지속형 ) 발효공정개발및스케일업모델링 스케일업수행 / 문제해결 바이오의약품의지속형플랫폼기술개발 생명공학, 생물화학공학, 고분자공학, 생화학및유사전공 산업체해당자우대 세부안내사항 1. 지원자격 - 석사이상학위자 ( 박사우대 ) - 은관련분야 3년이상 - 군필또는면제자로서해외여행에결격사유가없는자 2. 기타사항 - 국가보훈대상자및장애인은우대하여채용합니다. - 글로벌헬스케어그룹대웅은흡연자를채용하지않습니다.
녹십자 ( 목암생명과학연구소 ) 올해로창립 50 주년을맞이하는녹십자는각종우수의약품을생산, 공급하여국민건강생활에중요한역할을하며우리나라의생명공학산업을선도해온대표적인연구개발중심기업입니다. 녹십자는세계적신약개발에매진하며글로벌리더가되기위한창의와도전을멈추지않고있으며국제적인생명공학전문기업으로발돋움하고있습니다. 목암생명과학연구소는녹십자가세계에서세번째로개발에성공한 B 형간염백신을통해얻어진이익을기금으로출연해 1984 년에설립된연구소입니다. 목암생명과학연구소는생명공학기술발전을통한사회기여와이익창출을도모하고이를연구개발에재투자함으로써안정적이고지속적인연구환경을조성하기위한목적으로설립됐습니다. 우리나라민간연구기관으로는최초로과학기술처 ( 現미래창조과학부 ) 의승인을받아설립된비영리연구재단법인입니다. 녹십자와목암연구소에서아래와같이해외인재채용을진행하고자합니다. 많은관심부탁드립니다. 모집분야 업무내용 자격요건 필요서류 사업개발부 ( 바이오전공자, / 신입 ) 일반바이오연구직 해외사업본부 BD 팀 사업개발본부 Business 녹십자 / 목암연구소 해외사업본부 / BD 팀 Intelligence Team Vaccine, Immunology 사업개발본부 Open Innovation Team, 공정개발팀 Team Analysis of a new business/ 백신, 항암치료제개발 해외신규수출시장발굴 investment opportunity and 제형연구, 분석법개발 Market Research in establishment of business 동물세포배양및정제공정 Vaccine, strategies 개발 Immunodeficiency, Portfolio Optimization and market Autoimmune Diseas, and research Hemophilia Exploring R&D collaboration Management in Technolgy opportunities Transfer Project Early staged research pipeline licensing 학위 : 석사이상 학위 : 박사이상 학위 : PhD (PhD candidate) 전공 : 바이오및제약분야관련 전공 : 바이오및제약분야 전공 : Immunology, 전공자 관련전공자 Hematology, Virology 우대사항 : 우대사항 : 우대사항 : 어학우수자 어학우수자 어학우수자 전략기획 / 시장분석 / 사업개발 / 바이오텍종사자 Licensing 등의관련업무 유경험자 영문 CV 영문 CV 영문 CV
LG 화학생명과학사업본부 채용안내 LG화학생명과학사업본부는 혁신신약개발을통한글로벌제약사로의성장 을목표로지속적인연구개발을수행하고있습니다. 팩티브, 제미글로의합성의약품및백신, 바이오시밀러등의바이오의약품개발역량과경험을기반으로 Unmet Medical Needs를해결할수있는혁신신약개발연구를확대하고있습니다. LG화학에서혁신신약개발에함께하실열정과실행력을겸비한우수인재를모시고자합니다. 여러분들의많은관심과지원바랍니다. 감사합니다. 2017. 09
[ 2017 SK 바이오팜해외우수인재채용 ] 1. 모집대상 박사학위소지자 ( 취득예정자포함 ) 및 Post Doc./ Jr. 급연구원 남자의경우병역필또는면제자 2. 모집분야 구분중추신경계질환신약개발연구항암신약개발연구 내용 * 중추신경계질환신약후보물질설계및합성 * 신경 / 뇌질환관련과제도출 * 중추신경질환약효평가모델구축및운용 (in vitro & in vivo & ex vivo) * 약물의작용기전연구 * 항암제개발과제도출 * 외부도입항암제후보물질평가 * 항암제신약후보물질설계및합성 * 항암제약효평가모델구축및운용 (in vitro & in vivo & ex vivo) 연구분야 : Cancer Biology, Neuroscience, Biochemistry, Cell & Molecular Biology, Immunology, Pharmacology, Organic chemistry, Medicinal chemistry 등 신약개발관련전공 3. 지원방법 KASBP 담당자에게 CV 접수 4. 문의처 최우진선임 (choiwj@sk.com)
SK Life Science, Inc. SUMMARY OF POSITION The Senior Manager of CMC (Chemistry, Manufacturing and Controls)is Responsible and accountable for the development of CMC regulatory strategies, submissions, and compliance activities for biopharmaceutical development programs and commercial product(s). Supports/leads the preparation (writing submissions) of CMC information for submission to global regulatory agencies, generates CMC strategies, assesses risks and develops contingency plans. Act as the global CMC representative or contribute support to the Global CMC representative within cross functional project teams, involving the interpretation of regulations and guidelines and the assessment of global implication for strategic CMC decisions. Accountable for assigned CMC programs, managing day to day activities for specific projects. Depending on the experience, may operate independently to resolve complex issues and manage regulatory risks and ambiguous situations within project teams. Investigates opportunities for regulatory innovation/promote the use of novel approaches within project teams to resolve issues and problems. Creates/contributes to the development of internal policies, processes and procedures supporting progression and maintenance of the SK Life Sciences biopharmaceutical portfolio at large. Ability to collaborate effectively across a network of other stakeholders, partners and other departments, to deliver high quality CMC submissions and ensuring the compliance of the SK Life Science biopharmaceutical portfolio. Manages the resolution of regulatory CMC/information management issues with project/program stakeholders. Uses technical and scientific knowledge to conduct the appropriate analysis of CMC submission documentation. Reponsible for development of CMC documentation, coordination and management of global submissions, including assessment and management of labeling requirements.+ Able to develop and/or lead projects or team initiatives to support short term operational goals and contribute development of global regulatory initiatives. JOB REQUIREMENTS Ph.D, Pharm D, M.Sc. or MBA with formal Chemistry education including RAC certification Technical and scientific understanding of biopharmaceutical drug development with technical writing skills. Extensive experience (minimum 10 years+) leading CMC teams within a matrix environment Project Management training and experience required Successful candidate will be able to excel in a global multifunctional environment A working level understanding of the following: o Pharmaceutical industry API process and drug product development and GMP production o Pharmaceutical industry analytical method validations and stability requirements o Chemistry of pharmaceutical APIs and of analytical techniques for their characterization o Analytical knowledge using the latest state of the art systems and technologies e.g. HPLC, UV, IR, MS, NMR, XRD o Thorough understanding of cgmp, ICH and FDA requirements including global clinical product labelling requirements, submissions and individual regulatory requirements o Interact with global regulatory agencies as needed o Experience in preparing/oversight of CMC section for global regulatory submissions o Solid understanding in clinical trial materials requirements for global studies o Vendor Management, contracting, tracking, day-to-day interactions. Follow company policies and SOPs for vendor selection, funding requests and invoice processing o Ensuring company quality standards are met, assisting with audits as needed o Assist in due diligences as needed o Comfortable working in a virtual team environment over global time zones o Computer literate with MS Office Suite, SAP, and other business tools
브릿지바이오 (Bridge Biotherapeutics) 브릿지바이오는, 회사설립은 2015 년 9 월이고현재한국에 7 명, 미국 JLABS@TMC 에 1 명이직원이있으며, 최근시리즈 B 로 138 억원증자를마쳤습니다. 시리즈 A 를 2016 년에 145 억원을하여서, 2 년사이에총 283 억증자를하였습니다. 두개 NCE 의 P2a 까지의개발준비를최근마쳤습니다. 대표이정규박사님께서금요일밤늦게도착하여토요일일정중에브릿지바이오에대해궁금하시고함께일할기회에관심이있으신분 ( 특히사업개발혹은임상개발담당자 Position 관심이있으신분 ) 들과면담하기를원합니다. 관심이있으신분들은이정규대표님의 Facebook messenger 로 (James Jungkue LEE or posting at KASBP FB page 참조 ) 연락하시거나 james.lee@bridgebiorx.com 으로연락하시기바랍니다. 연락이어려우시면 KASBP Job Fair 담당자에게연락하시기바랍니다.
큐라켐 (Curachem) Established in 2009, Curachem is a global provider of custom synthesis of 14C radiolabeled, 3H radiolabeled and stable-isotope labeled compounds. Curachem is a fast- growing, successful and profitable organization with a team of dedicated and highly experienced chemists from pharmaceutical company and contract research organization backgrounds. As a customer-focused company, we design our services to support our clients and meet their requirements in order to reduce cost and increase productivity. Curachem is conveniently located near Seoul, Korea and has convenient access to two major airports for international shipping. Our 3,000 square feet of space houses well-equipped and modern chemical and radiochemical laboratories. Curachem Inc. 207, Osongsaengmyeong 1-ro, Osong-eup, Heungdeok-gu, Cheongju-si, Chungcheongbuk-do, 28161, Republic of Korea -Job description- 1. Organic chemist with master or higher degree 2. Fluent English in speaking and writing 3. prefer 3+ yrs chemistry experience but will interview no experience, too. Please send your resume to 신숙정 sjshin@curachem.com for an interview during 2017 KASBP Fall Symposium on Friday (4-5:30 pm) or Saturday.