JOB BOARD SPOTLIGHT FROM THE PETRIDISH Production Technician / Environmental Compliance Coordinator / Quality Control Chemist - BIOVECTRA Research Technician - Ottawa Hospital Research Institute Sr. Process Engineer - Eurofins CDMO Alphora Inc. Gestionnaire Comptes Clés – Myélome Multiple / Gestionnaire régional de l’écosystème, Québec et Atlantique / Key Account Specialist – Oncology – Quebec East /Nova Scotia / Medical Science Liaison Vaccines / Regional Ecosystem Manager, Québec and Atlantic / Critical Materials Management Assistant – VIE Contract - Sanofi Executive Assistant/Office Manager / Senior Scientist, CMC, Drug Product - Xenon Pharmaceuticals Inc. Research Associate I, Immunology / Research Associate II, Immunology / Senior Manager GLP Quality Assurance / Senior Project Manager / Senior Scientist, Drug Safety - Zymeworks Inc. Please apply directly with the employer. Job postings are available at <https://bit.ly/46KPrqn> Veuillez postuler directement auprès de l'employeur. Les offres d'emploi sont disponibles sur le site <https://bit.ly/46KPr9R> Are you looking for new and better ways to recruit talent? Contact Soufiane at [info@biotalent.ca]<mailto:info@biotalent.ca> to learn more.
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#GSK is currently hiring 𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐨𝐫𝐲 𝐀𝐟𝐟𝐚𝐢𝐫𝐬 𝐒𝐩𝐞𝐜𝐢𝐚𝐥𝐢𝐬𝐭. Position is based in 𝐁𝐨𝐮𝐦𝐞𝐫𝐝𝐞𝐬. 𝐁𝐚𝐬𝐢𝐜 𝐐𝐮𝐚𝐥𝐢𝐟𝐢𝐜𝐚𝐭𝐢𝐨𝐧𝐬: • Bachelor’s degree of pharmaceutical science is a must. • Min. one-year of experience in similar job within pharma industry. • Good command of English language. 𝐏𝐫𝐞𝐟𝐞𝐫𝐫𝐞𝐝 𝐐𝐮𝐚𝐥𝐢𝐟𝐢𝐜𝐚𝐭𝐢𝐨𝐧𝐬: • Master’s degree. • Excellent verbal and written communications skills. • Ability to work carefully under time constraints and prioritize accordingly. • Adaptable to fast-paced environments with changing circumstances, direction, and strategy. • Exposure to work within a regulated environment, ideally in drug development. 𝐅𝐨𝐫 𝐦𝐨𝐫𝐞 𝐝𝐞𝐭𝐚𝐢𝐥𝐬 𝐨𝐫 𝐭𝐨 𝐚𝐩𝐩𝐥𝐲, 𝐅𝐨𝐥𝐥𝐨𝐰 𝐭𝐡𝐞 𝐥𝐢𝐧𝐤: (https://lnkd.in/eBYpsBVj). ---
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#ABBOTT is currently hiring a 𝐌𝐞𝐝𝐢𝐜𝐚𝐥 𝐑𝐞𝐩𝐫𝐞𝐬𝐞𝐧𝐭𝐚𝐭𝐢𝐯𝐞 based in 𝐁𝐚𝐭𝐧𝐚. 𝐑𝐞𝐪𝐮𝐢𝐫𝐞𝐦𝐞𝐧𝐭𝐬: • Science degree ( biologist, pharmacist, medicine………..). • 2 years’ experience in pharmaceutical company. 𝐅𝐨𝐫 𝐦𝐨𝐫𝐞 𝐝𝐞𝐭𝐚𝐢𝐥𝐬 𝐨𝐫 𝐭𝐨 𝐀𝐩𝐩𝐥𝐲, 𝐅𝐨𝐥𝐥𝐨𝐰 𝐭𝐡𝐞 𝐥𝐢𝐧𝐤: (https://lnkd.in/dSYEKCaE).
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Pharma Career Expert | Professional Speaker | Helping Healthcare Professionals Land high-paying Corporate jobs through Interview Coaching & Personal Branding
The Pharmaceutical industry is a dynamic and ever-evolving field. It offers a wealth of opportunities for job seekers. From research and development to regulatory affairs, medical affairs, sales, and marketing, there is a wide range of roles to suit various skill sets and interests. With advancements in biotechnology, personalised medicine, and digital health, the industry is at the forefront of innovation. This not only means a chance to work on groundbreaking projects but also a stable and rewarding career path. If you're passionate about improving healthcare and making a difference in people's lives, now is the perfect time to explore a career in Pharma. Learn more about what it takes to start your career in this exciting field💊🚀 by joining this live webinar. You will find the link to this event in the comments below. 👇
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★☆ Global 제약사 분자진단 RA Manager (부장급) ==> closing !! [업무내용] MD(Molecular Diagnostics) RA Manager 담당 - As an individual contributor, the function of a Regulatory Affairs Manager is to provide support for the regulatory department to ensure efficient and compliant business processes and environment. - The individual may execute tasks and play a consultative role by partnering across business functions. - The individual may assist in identifying data needed, obtaining these data and ensuring that they are effectively presented for the registration of products worldwide. - The individual may prepare and submit documentation needed for registration worldwide or may oversee such preparation. [자격조건] 1. 학사이상. Science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields is preferred. 2. 진단 관련 경력 최소 4년 이상, total 경력 10년 이상. 3. 영어 가능자(미국팀과 call 자주 있음) [근무조건] 1. 급여: 기존 + @, 면접 후 협의 (ABS, Target Incentive) 2. 근무지: 서울 강남구 * 관심 있으시면...연락주세요 (주)SCOUT 헤드헌팅사업부문 정경 전무 // 010-4201-0264 // chogosu@scout.co.kr SCOUT Co., Ltd. / Headhunting Div./ Senior Director #MD(Molecular Diagnostics) #Regulatory Affairs #molecular biology techniques
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#Amgen is currently hiring: 𝟏- 𝐁𝐢𝐨𝐩𝐡𝐚𝐫𝐦𝐚𝐜𝐞𝐮𝐭𝐢𝐜𝐚𝐥 𝐑𝐞𝐩𝐫𝐞𝐬𝐞𝐧𝐭𝐚𝐭𝐢𝐯𝐞 (𝐄𝐚𝐬𝐭 𝐑𝐞𝐠𝐢𝐨𝐧). (https://lnkd.in/eB7wUmuZ). 𝟐- 𝐁𝐢𝐨𝐩𝐡𝐚𝐫𝐦𝐚𝐜𝐞𝐮𝐭𝐢𝐜𝐚𝐥 𝐑𝐞𝐩𝐫𝐞𝐬𝐞𝐧𝐭𝐚𝐭𝐢𝐯𝐞 (𝐖𝐞𝐬𝐭 𝐑𝐞𝐠𝐢𝐨𝐧). (https://lnkd.in/eQYS-HGH). 𝐌𝐢𝐧𝐢𝐦𝐮𝐦 𝐑𝐞𝐪𝐮𝐢𝐫𝐞𝐦𝐞𝐧𝐭𝐬: • Minimum 3 to 5 years of experience in the pharmaceutical industry in a sales-related job. • Experience in a hospital environment. • Some experience with computer systems (CRM databases and MS Office). • Fluency in local language, both in oral and written communication. • Relevant local legal qualification. 𝐏𝐫𝐞𝐟𝐞𝐫𝐫𝐞𝐝 𝐑𝐞𝐪𝐮𝐢𝐫𝐞𝐦𝐞𝐧𝐭𝐬: • Bachelor’s degree in life science or (bio) medical sciences. • Knowledge of Customer Relation Management principles. • Exposure to interactions with various disciplines and organizational levels. • Exposure to project management principles. ---
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Calling all professionals with a #PharmD, MS in #PublicHealth, or BS in #Pharmacology, #Pharmacy, #Biochemistry, Biology, Chemistry, or #Biomedical Sciences! Are you aiming for that long-awaited #promotion, seeking to #enhance your #expertise, or move into a different career area, now is the time to invest in yourself. Explore our Master's degree in #Clinical #Research #Management with a focus on Drug Safety and Pharmacovigilance! https://lnkd.in/eRnSprag Gain expertise in risk and signal management while advancing your professional skills. No GRE required. Gain hands-on experience. Apply before the Monday, April 15th deadline now to secure your spot for Fall 2024 admissions and pave the way for your future success! https://lnkd.in/eRnSprag Don't miss out on this chance to redefine your career path. Limited spots available! #MasterYourFuture #CareerGrowth #ProfessionalDevelopment #Pharmaceutical #MedicalDevices #DrugSafety #Pharmacovigilance #MasterYourFuture #CareerGrowth #VirtualInfoSession #newcareer #promotion #nurses #biology #chemistry #fda #labeling #qualitymanagement #compliance #DEI #decentralized #projectmanagement
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#Adamco_Pharm is hiring a 𝐒𝐞𝐧𝐢𝐨𝐫 𝐏𝐫𝐨𝐝𝐮𝐜𝐭 𝐌𝐚𝐧𝐚𝐠𝐞𝐫. Position based in 𝐀𝐥𝐠𝐢𝐞𝐫𝐬. 𝐑𝐞𝐪𝐮𝐢𝐫𝐞𝐦𝐞𝐧𝐭𝐬: • Bachelor's degree in pharmacy, Medicine, or Veterinary Medicine. • 3+ years of relevant work experience in the generic pharmaceutical industry. • A business or Marketing diploma degree will be a plus. • French language proficiency is a Must. • Excellent Communication & Presentation skills. 𝐅𝐨𝐫 𝐦𝐨𝐫𝐞 𝐝𝐞𝐭𝐚𝐢𝐥𝐬 𝐨𝐫 𝐭𝐨 𝐚𝐩𝐩𝐥𝐲, 𝐅𝐨𝐥𝐥𝐨𝐰 𝐭𝐡𝐞 𝐥𝐢𝐧𝐤: (https://lnkd.in/d7VXypeF). --- 𝘼𝒅𝙖𝒎𝙘𝒐 𝑷𝙝𝒂𝙧𝒎 𝑖𝑠 𝑎 𝑓𝑎𝑠𝑡 𝑔𝑟𝑜𝑤𝑖𝑛𝑔 𝑖𝑛𝑡𝑒𝑟𝑛𝑎𝑡𝑖𝑜𝑛𝑎𝑙 𝑃ℎ𝑎𝑟𝑚𝑎𝑐𝑒𝑢𝑡𝑖𝑐𝑎𝑙 ℎ𝑜𝑙𝑑𝑖𝑛𝑔 𝐶𝑜𝑚𝑝𝑎𝑛𝑦 𝑏𝑎𝑠𝑒𝑑 𝑖𝑛 𝐶𝑎𝑖𝑟𝑜 - 𝐸𝑔𝑦𝑝𝑡. ---
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#NewBridge_Pharmaceuticals is hiring a 𝐌𝐞𝐝𝐢𝐜𝐚𝐥 𝐒𝐜𝐢𝐞𝐧𝐜𝐞 𝐋𝐢𝐚𝐢𝐬𝐨𝐧. The position is based in 𝐀𝐥𝐠𝐢𝐞𝐫𝐬. 𝐑𝐞𝐪𝐮𝐢𝐫𝐞𝐝 𝐂𝐨𝐦𝐩𝐞𝐭𝐞𝐧𝐜𝐢𝐞𝐬, 𝐐𝐮𝐚𝐥𝐢𝐟𝐢𝐜𝐚𝐭𝐢𝐨𝐧𝐬 𝐚𝐧𝐝 𝐄𝐱𝐩𝐞𝐫𝐢𝐞𝐧𝐜𝐞: • Bachelor Degree in Medicine, Pharmacy, Dentistry or other life science. • Master Degree or Master of Business Administration is desirable. • Minimum of 1 year of experience as Medical Science Liaison, Medical advisor or Clinical research associate in a Multinational Pharmaceutical Company in the AfMET region (Africa, Middle-East and Türkiye) is required. • Previous experience as medical representative and/or commercial role is desirable in a Multinational Pharmaceutical Company. • Previous experience working with Multiple Sclerosis is preferred but not essential. 𝐅𝐨𝐫 𝐚𝐝𝐝𝐢𝐭𝐢𝐨𝐧𝐚𝐥 𝐝𝐞𝐭𝐚𝐢𝐥𝐬 𝐨𝐫 𝐭𝐨 𝐚𝐩𝐩𝐥𝐲, 𝐅𝐨𝐥𝐥𝐨𝐰 𝐭𝐡𝐞 𝐥𝐢𝐧𝐤: (https://lnkd.in/eh_c8Db9). ---
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Good Opportunity
AH pharma Research center committed to providing outstanding medical research services for drug industry is seeking a skilled and dedicated Pharmacist to join our team....... Position : Data processing & medical writing specialist Qualification: Pharmacist /Chemist 1-3 years experience Location: Hadayek Elahram Type: Full-time Responsibilities: 1-Conduct comprehensive literature and fulfill the requirements of pharmaceutical research. 2-Write and Review the Scientific Medical data, covering all phases of clinical research for submission to regulatory agencies 3-Preparation of Final study report of In-vitro comparative dissolution studies. • Preparation of Final study report of Bioequivalence studies including the documentation of clinical steps, scientific data of the investigated product, summaries of (PK, Statistical results), bio analytical method validation and in vitro testing results. 4-Preparation of final study files of BE/BW studies including report and all related document Requirements. To apply, please submit your CV and any relevant certifications to [hendfathy336@gmail.com] We will review applications on a rolling basis and contact qualified candidates for interviews.
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