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| Jobs in biotechnology,
pharmaceutical, medical devices and life sciences
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Welcome to
BiotechJobs!
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BiotechJobs.co.il is the
Internet’s leading recruitment portal for the
Biotechnology,
Pharmaceutical, Medical Devices
and Life Sciences industries in Israel.
Whether you are a graduate or currently employed
scientist looking for jobs in science, biotechnology,
chemical engineering, pharmaceutical sales,
bioinformatics, chemistry, academic posts, or medical
careers this is the place for you to search for
vacancies and submit your resume.
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Senior Protein Purification Scientist |
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Education: |
Masters |
Position type: |
Full Time |
Experience: |
6 years |
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Area(s) of expertise desired: |
Academic, Biochemistry, Laboratory, Molecular Biology, Process Development, Project Management, Protein Chemistry, Research, Protein Purification
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Description: |
Fantastic Farms is a fast-paced biotechnology-oriented food-tech company, working to change how humanity is making food. Fantastic Farms is a pioneer in the alternative proteins landscape, as we are harvesting the power of plants to produce animal proteins and use them to recreate dairy and eggs. We put our heart, soul, and skills into making a difference for people, animals and the planet.
This is a new role that requires someone highly-motivated, energetic and an excellent team player focused on creating disruptive technology in the lab. The work requires hands-on process development for protein extraction, purification and characterization from plants.
Working together to push the boundaries, we blend the best of our talents to unlock innovation. We welcome you to join us in our adventure. Location: Tel-Aviv.
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Requirements: |
M.Sc or Ph.D. in Life Sciences/Chemistry/Biochemistry with at least 6 years of industry experience
Expertise in protein purification demonstrated through purification of several types of proteins using a wide range of methods for at least 4 years hands on experience
Ability to perform and interpret protein analytical assays such as SDS-Page, WB, ELISA, HPLC
Independently develop new purification protocols, identify and resolve product and production related issues
Self-starter and highly independent individual comfortable to work under pressure and deadlines
Passionate to perform cutting edge protein science, using advanced laboratory equipment
Flexibility to work varying schedules and hours as needed according to changing deadlines
Industrial experience and demonstrated success in process and product development, scale-up - advantage
Familiarity with ISO9000, or cGMPs - advantage
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Senior Protein Purification Scientist |
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Education: |
Masters |
Position type: |
Full Time |
Experience: |
6 years |
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Area(s) of expertise desired: |
Academic, Biochemistry, Laboratory, Molecular Biology, Process Development, Project Management, Protein Chemistry, Research, Protein Purification
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Description: |
Fantastic Farms is a fast-paced biotechnology-oriented food-tech company, working to change how humanity is making food. Fantastic Farms is a pioneer in the alternative proteins landscape, as we are harvesting the power of plants to produce animal proteins and use them to recreate dairy and eggs. We put our heart, soul, and skills into making a difference for people, animals and the planet.
This is a new role that requires someone highly-motivated, energetic and an excellent team player focused on creating disruptive technology in the lab. The work requires hands-on process development for protein extraction, purification and characterization from plants.
Working together to push the boundaries, we blend the best of our talents to unlock innovation. We welcome you to join us in our adventure. Location: Tel-Aviv.
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Requirements: |
M.Sc or Ph.D. in Life Sciences/Chemistry/Biochemistry with at least 6 years of industry experience
Expertise in protein purification demonstrated through purification of several types of proteins using a wide range of methods for at least 4 years hands on experience
Ability to perform and interpret protein analytical assays such as SDS-Page, WB, ELISA, HPLC
Independently develop new purification protocols, identify and resolve product and production related issues
Self-starter and highly independent individual comfortable to work under pressure and deadlines
Passionate to perform cutting edge protein science, using advanced laboratory equipment
Flexibility to work varying schedules and hours as needed according to changing deadlines
Industrial experience and demonstrated success in process and product development, scale-up - advantage
Familiarity with ISO9000, or cGMPs - advantage
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Senior Protein Purification Scientist |
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Education: |
Masters |
Position type: |
Full Time |
Experience: |
6 years |
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Area(s) of expertise desired: |
Academic, Biochemistry, Laboratory, Molecular Biology, Process Development, Project Management, Protein Chemistry, Research, Protein Purification
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Description: |
Fantastic Farms is a fast-paced biotechnology-oriented food-tech company, working to change how humanity is making food. Fantastic Farms is a pioneer in the alternative proteins landscape, as we are harvesting the power of plants to produce animal proteins and use them to recreate dairy and eggs. We put our heart, soul, and skills into making a difference for people, animals and the planet.
This is a new role that requires someone highly-motivated, energetic and an excellent team player focused on creating disruptive technology in the lab. The work requires hands-on process development for protein extraction, purification and characterization from plants.
Working together to push the boundaries, we blend the best of our talents to unlock innovation. We welcome you to join us in our adventure. Location: Tel-Aviv.
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Requirements: |
M.Sc or Ph.D. in Life Sciences/Chemistry/Biochemistry with at least 6 years of industry experience
Expertise in protein purification demonstrated through purification of several types of proteins using a wide range of methods for at least 4 years hands on experience
Ability to perform and interpret protein analytical assays such as SDS-Page, WB, ELISA, HPLC
Independently develop new purification protocols, identify and resolve product and production related issues
Self-starter and highly independent individual comfortable to work under pressure and deadlines
Passionate to perform cutting edge protein science, using advanced laboratory equipment
Flexibility to work varying schedules and hours as needed according to changing deadlines
Industrial experience and demonstrated success in process and product development, scale-up - advantage
Familiarity with ISO9000, or cGMPs - advantage
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Bioanalytical / Research and Development |
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Education: |
Bachelors |
Position type: |
Full Time |
Experience: |
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Area(s) of expertise desired: |
Bioanalytical Services, Biochemistry, Biology, Chemistry, Clinical Research, Pharmacology
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Description: |
Entera Bio, a Jerusalem based, clinical-stage small biopharmaceutical company focused on oral delivery of large molecules is recruiting an employee to join their research and development team. Located in Hadassah Ein Kerem.
Job opportunity entails hands-on bioanalytical lab work, developing study reports, and overall R&D support. The position is a maternity leave replacement position, with potential to extend.
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Requirements: |
Requirements:
• B.Sc/M.Sc in biology, pharmacology, or medical sciences
• Lab experience (preferably experience with bioanalytical ELISA kits)
• Scientific writing capabilities
• High proficiency in English
• Hard-working, organized, attention to detail, and fast learner
Advantages:
• English Mother-tongue
• Experience and/or familiarity with drug development (Pre-clinical/clinical/ regulatory)
• Experience with in-vivo models
• Background in regulatory submissions
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Healthtech & life science positions across aMoon Fund Portfolio |
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Category: |
QA - Quality Control, Chemistry
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Education: |
Doctorate |
Position type: |
Full Time Employee |
Experience: |
2 years |
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Area(s) of expertise desired: |
Academic, Administration, Analytical Chemistry, Applied Chemistry, Biochemistry, Bioinformatics, Biology, Business Analyst, Business Development, Chemistry, Clinical Data Management, Clinical Research, Executive, Finance, GLP, GMP, Human Resources, Manufacturing/Production, Medical Affairs, Medical Device, Molecular Biology, Neurosciences, Nutrition, Orthopedics, Pharmacokinetics, Pharmacology, Postdoctoral, Process Development, Production Planning, Professional Services, Project Management, Purchasing, Quality Control, Radiology, Regulatory Affairs, Research, Start-Up, Technical Services
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Description: |
aMoon is a leading Israeli venture capital. We invest in companies that are accelerating cures for the world’s most life-threatening conditions and providing solutions for global healthcare’s biggest cost drivers. Our mission is to identify, invest, and drive growth in companies of all development stages across biopharmaceutical, device, and digital technologies.
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Requirements: |
With over 30 local vacancies in leading healthtech & life sciences companies we encourage you to visit our job board!
https://jobs.amoon.fund/
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Healthtech & life science positions across aMoon Fund Portfolio |
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Category: |
QA - Quality Control, Chemistry
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Education: |
Doctorate |
Position type: |
Full Time |
Experience: |
2 years |
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Area(s) of expertise desired: |
Academic, Biochemistry, Biology, Business Analyst, Business Development, Cell Biology, Clinical Data Management, Clinical Research, Communications, Genetics, GMP, Human Resources, Immunology, Infectious Disease, Internal Medicine, Manufacturing/Production, Marketing, Medical Device, Neurosciences, Pharmacology, Postdoctoral, Process Development, Production Planning, Professional Services, Project Management, Quality Assurance, Quality Control, Regulatory Affairs, Research, Sales, Software Development, Start-Up
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Description: |
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aMoon is a leading Israeli venture capital. We invest in companies that are accelerating cures for the world’s most life-threatening conditions and providing solutions for global healthcare’s biggest cost drivers. Our mission is to identify, invest, and drive growth in companies of all development stages across biopharmaceutical, device, and digital technologies.
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Requirements: |
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With over 30 local vacancies in leading healthtech & life sciences companies we encourage you to visit our job board!
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Clinical trials site manager |
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Category: |
Clinical trials
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Education: |
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Position type: |
Full Time Manager |
Experience: |
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Area(s) of expertise desired: |
Biology, Clinical Research, Medical Affairs, Medical Device, Research
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Description: |
nRollmed, an online clinical trials recruitment agency, is seeking a professional to fill the role of a clinical sites manager, to begin in January or February 2020.
Develop relationships with teams at clinical sites in the U.S. and oversee their recruitment activities
Manage a team of nRollmed recruitment agents who screen patients for studies.
Full time position
Partially work from home. In Tel Aviv office 2-3 times a week
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Requirements: |
Exceptional interpersonal skills and the ability to manage many people and tasks at once.
English as mother tongue
Excellent written English
Ability to work US hours
Academic or professional experience in the fields of life sciences and healthcare required.
CRA/GCP certification an advantage
To apply, please submit your CV to gil.pal@nrollmed.com.
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Clinical trials recruitment agent |
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Education: |
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Position type: |
Part Time |
Experience: |
No experiece |
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Area(s) of expertise desired: |
Biology, Clinical Research, Pharmacology, Research
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Description: |
nRollmed, an online patient recruitment & retention company, is seeking professionals to conduct phone screenings of potential patients considering participation in clinical trials.
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Requirements: |
Meticulous record keeping and administrative capabilities
High level of interpersonal communication and sensitivity required. Ability to build trust and confidence over the phone.
Academic or professional experience in the fields of life sciences and healthcare required.
Medical and nursing school students welcome to apply.
CRA/GCP certification an advantage.
English as mother tongue
Ability to work US hours
Work from home
The job will approximate to part time (around 20 hours a week), but the daily amount of hours will vary based on the number of patients who express interest in a given trial.
To apply, please submit your CV to gil.pal@nrollmed.com.
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Work as a software developer without experience - for graduate students |
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Category: |
Biotechnology, Engineering, Chemistry, Life Sciences, Pharmacy/Pharmacology, Healthcare, IT/Hardware/Software
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Education: |
Bachelors |
Position type: |
Full Time |
Experience: |
No experiece |
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Area(s) of expertise desired: |
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Description: |
InfinityLabs R&D(a Matrix company) is looking for Graduates with high grades who want to develop a career! You have the option to change your future by 180 degrees. If you have high analytical capabilities and you are interested to work in the high-tech industry - this is your chance to try your luck and test your suitability for work as a software developer. Qualifying will be given training at the expense of the company.
Full-time job.
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Requirements: |
Bachelor's degree average of 85 and above.
Independent learning ability.
high-level English.
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Director, Clinical Operations |
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Category: |
Life Sciences, Clinical Research, Pharmacy/Pharmacology
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Education: |
Bachelors |
Position type: |
Full Time |
Experience: |
10+ years |
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Area(s) of expertise desired: |
Clinical Research, Regulatory Affairs, Start-Up
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Description: |
The Role:
Reporting to the Senior Director, Clinical Operations & Site Head, the Director of Clinical Operations will be responsible for leading and managing the execution of Eloxx’s clinical studies from protocol inception through study closure. This key role will manage, plan and execute clinical studies, including creating and managing study timelines, budgets and study management plans in a full out-sourced model to ensure that our corporate goals. This is a great opportunity for visibility and professional growth; the Director of Clinical Operations will manage a team of Clinical Project Managers and partner with the Senior Director to represent the Clinical Operations team cross-functionally and with key stakeholders.
Responsibilities:
• Ensures that clinical trial projects are properly resourced, managed and executed within budget and in accordance with established timelines and quality standards.
• Oversees the day-to-day clinical operations through a team of Project Managers with a focus on vendor management(e.g., CRO, laboratories), monitoring clinical trial recruitment rate, and coordination of activities.
• Executes high quality, integrated cross-functional plans for the project/clinical trial.
• Represent Clinical Operations in cross-functional teams, clinical meetings and regulatory meetings. Provide regular status updates to senior management.
• Provide strategic input and drive the planning and execution for assigned clinical trials with direct responsibility for time, cost, quality, and risk mitigation.
• Responsible for the oversight of protocols development; protocol preparation, amendments, CRF, informed consent form, operations and other documentation required for conduct of a clinical trial.
• Accountable for internal clinical trial files and documents.
• Participates and manages investigator meetings and follow up.
• Travels for meetings and site visits when necessary.
• Maintains proper communications with other departments to ensure good relationships in connection with ongoing set up and progress throughout trial planning and execution.
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Requirements: |
Competencies Include:
• Complex problem-solving abilities with a focus on accomplishing assigned goals and objectives in a dynamic environment.
• A team player who is able to effectively and flexibly lead cross functional teams across diverse cultures, backgrounds and styles.
• Excellent communications and presentation skills, able to effectively inform key stakeholders and management of the status, issues and solutions.
• Strong organizational and planning skills are required, with a proven ability to manage budgets and timelines.
• Detail-oriented, a self-starter and comfortable with broad responsibilities in a fast-paced, small company environment.
• Excellent computer skills, proficiency with project management software tools.
• Prepared to travel internationally (US and EU) for approximately 7-10 days once every 2-3 months.
• Flexibility to work US hours a few times a week.
Experience:
• Minimum of 10 years’ experience in the pharmaceutical industry, with 5-7 years’ direct experience in planning and managing global clinical trials.
• Strong people management skills with experience managing at least 2 or 3 direct reports required.
• Strong bi-lingual verbal and writing skills in English and Hebrew required.
• Extensive experience managing clinical programs, CROs, budgets and timelines.
• Regulatory/EMA/FDA experience.
• Good working knowledge of medical terminology, physiology and pharmacology and an excellent knowledge of applicable U.S. and international regulations and guidelines.
• Solid understanding of pharmaceutical clinical development processes and have experience with clinical monitoring.
• Ability to thrive in a fast-paced, entrepreneurial environment with busy, high performing colleagues.
• Strong leadership skills and self-awareness.
• Experience presenting to a varied audience, including investors and upper management.
Education:
• Bachelor’s Degree or equivalent biologic science degree is preferred.
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מטפלת מאגר מטפלות לילדים , אופרייות
לוח
דרושים הגדול בישראל כולל אלפי הצעות עבודה | |
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