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Job Search Results: Jobs 11 - 20 of 179  View Titles & Details  Page 2 of 18
 
Title   Company Name     Location   Date  
Lab manager / Research scientist 

  Technion Faculty of Medicine    North Area, Haifa   15/3/2017 
Category: Life Sciences  
Education: Doctorate   Position type: Full Time Employee  Experience:  
Area(s) of expertise desired: Academic, Biology, Genomics, Molecular Biology, Research  
Description:
The Lab of Genome Structure and Function is seeking an excellent lab manager or research scientist. Our lab, at the Technion Faculty of Medicine (within walking distance of Bat Galim train station), uses a combination of advanced computational and experimental methods to study the profound connection between genetic information and its physical organization.

Our goal is to decipher how the genome encodes its 3D organization, and how this organization mediates biological function.

For further information about the lab, see: https://kaplanlab.net.technion.ac.il

 
Requirements:
We are seeking an outstanding lab manager or research scientist with a PhD in molecular biology. Experience in genomics, sperm, mammalian cells or CRISPR is an advantage.
 
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Patient recruitment for clinical trials 

  nRollmed Ltd.    All, all over   27/11/2016 
Category: Clinical Research, Clerical/Administrative, Sales/Marketing  
Education: Associate   Position type: Part Time  Experience: No experiece 
Area(s) of expertise desired: Administration, Clinical Research, Communications, Customer Service, Marketing, Sales, Technical Services  
Description:
nRollmed - online patient recruitment & retention, is seeking for professionals to conduct phone pre-screening of potential patients considering participation in clinical trials.

 
Requirements:
high marketing capabilities
ability to build trust and confidence over the phone
active listening and empathy
availability during different hours of the day
administrative capabilities
experience in clinical trials - an advantage

This job is suitable for those looking for a partial position and wishing to work from home. For more details please contact Hagit Nof at 054-4708077, hagit.nof@nrollmed.com
 
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SENIOR SCIENTIST IN BIOLOGICAL MANUFACTURING 

  SuperMeat    Jerusalem Area, Jerusalem   13/11/2016 
Category: Biotechnology  
Education:   Position type: Full Time  Experience: 2 years 
Area(s) of expertise desired: Biology, Cell Biology, Cell Culture  
Description:
SuperMeat is a groundbreaking biotechnology start-up that develops machines to organically grow chicken meat using cutting-edge regenerative technologies. The company was founded to address the technological and ecological challenges in feeding a growing global population. SuperMeat is an ideologically and scientifically driven effort to create a humane, animal-free solution to nutritional security that will drastically reduce carbon emissions while increasing food safety worldwide.

The Senior Scientist will work independently and as part of a team to develop large-scale culture methods for chicken mesenchymal cells, as well as a novel organ perfusion device. The Senior Scientist will be responsible for producing scientific progress reports and funding applications.

Candidates for the position must have a PhD and extensive research or industrial experience in biological manufacturing and mammalian cell biology. The candidate must show strong technical knowledge and expertise in industrial manufacturing of antibodies, proteins or vaccines in mammalian cells. Hands-on, wet-lab research and operation/care of instrumentation is required for this position. Specific experience in tissue engineering or stem cell biology is preferred. Candidate must have excellent oral and written communication skills in English, a strong work ethic, and a track record of meeting deadlines.
 
Requirements:
PhD in biology, bioengineering, chemical engineering or a related area
5+ years experience in stem cell biology, tissue engineering or closely related field required
2+ years industry experience in biological manufacturing required
Excellent ability to maintain detailed documentation
Highly motivated, creative, and devoted to project goals
Able to communicate effectively with colleagues and management teams
 
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Director of Quality Assurance 

  Salzman Capital Ventures, Ltd.    North Area, Katzrin   11/8/2016 
Category: Biotechnology  
Education: Doctorate   Position type: Full Time  Experience: 5 years 
Area(s) of expertise desired: Biochemistry, Chemistry  
Description:
Salzman Capital Ventures is seeking a Director of Quality Assurance to fill a post at our biotechnology laboratory in Kazrin, in the Golan Heights.

Responsibilities will include operation and leadership of a multinational quality assurance system in the pharmaceutical arena.
 
Requirements:
Position will require at a minimum a Ph.D. with experience creating and working with small molecules. Candidates must live in northern Israel with preference given to individuals living in the Golan. Must have near native English with excellent writing skills.  
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Synthetic Organic Chemists 

  Salzman Capital Ventures, Ltd.    North Area, Kazrin   11/8/2016 
Category: Biotechnology  
Education: Masters   Position type: Full Time  Experience: 3 years 
Area(s) of expertise desired: Chemistry  
Description:
Salzman Capital Ventures is seeking Synthetic Organic Chemists to join our team of 10 scientists in a drug development biotechnology laboratory in Kazrin, in the Golan Heights. The successful candidate will synthesize novel drugs and related compounds.  
Requirements:
MS or PhD in Chemistry
Near native English Proficiency
 
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Analytical chemist 

  Salzman Capital Ventures, Ltd.    North Area   11/8/2016 
Category: Staff Chemist  
Education: Masters   Position type: Full Time Employee  Experience: 3 years 
Area(s) of expertise desired: Chemistry  
Description:
Salzman Capital Ventures is seeking Analytical Chemists to join our team of 10 scientists in a drug development biotechnology laboratory in Kazrin, in the Golan Heights. The successful candidate will perform HPLC and Mass Spec on novel compounds and metabolites.



 
Requirements:
MSc or PhD in Chemistry
Near native English Proficiency  
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CRA 

  Notal Vision    Tel Aviv Area, Tel Aviv   1/8/2016 
Category: Clinical Research  
Education: Bachelors   Position type: Full Time  Experience:  
Area(s) of expertise desired: Clinical Research  
Description:

Responsible for all administrative support
in the clinical research department
Involved in the execution of clinical studies and documentation of findings according to established company guidelines
Responsible for ongoing data entry using IT systems, as well as other administrative supports
 
Requirements:
A degree or equivalent in a scientific or healthcare discipline.
Certified Clinical Research Associate (CRA)
Knowledge and understanding of medical facilities.
Exceptional interpersonal skills.  
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Clinical and Quality Assurance Manager 

  Trendlines Group    North Area, Misgav Industrial Park ( Near Carmiel)   27/7/2016 
Category: QA - Quality Control, Clinical Research  
Education:   Position type: Full Time  Experience: 5 years 
Area(s) of expertise desired: Clinical Research, Medical Device, Orthopedics, Quality Assurance, Start-Up  
Description:
Manages all clinical aspects of a clinical study, including:
Assesses operational feasibility and recommends study execution plan; participates in site monitoring visits as appropriate.
Select countries and sites for trial participation; develops relationships with K.O.L and site staff; coordinates and assists in the planning of regulatory or ethics committee activities, as appropriate;
Design clinical trial protocols;

Prepares/reviews site study documents
Manages clinical monitoring activities (including approval of visit report templates, monitoring plan, etc.)
Ensures all clinical trials are executed in compliance with ICH/GCP guidelines/regulations and applicable SOPs:
Manages all aspects of quality assurance activities including:
Ensure compliance with FDA and other regulatory affairs
Develop, administer and maintain quality assurance procedures and activities required to ensure that the companys processes and products are in compliance with applicable quality standards and requirements
Establish quality assurance and quality control inspection and testing procedures
 
Requirements:
Minimum 5 years clinical trial management experience in a medical device company - Mandatory
Advanced knowledge of Good Clinical Practices and current knowledge of FDA regulations for clinical trials is required;
International clinical trial experience
Minimum 2 years Quality Assurance experience in a medical device company - Mandatory
Thorough knowledge of FDA Quality System requirements, ISO 13485:2003 (Quality System) requirements
Knowledge of Good Manufacturing Practices (GMP) and applicable Quality System Standards
Experience working with subcontractors
Excellent English - written and verbal
Excellent communication and organizational skills, along with problem solving,

Travel- Travel abroad required per week, per month

Location: Misgav Industrial Park
 
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Marcom manager 

  Medasense    Tel Aviv Area   7/7/2016 
Category: Sales/Marketing  
Education:   Position type: Full Time  Experience: 3 years 
Area(s) of expertise desired:  
Description:
Medasense is looking for a marcom manager to join our dynamic and fast-paced environment!
 
Requirements:
Requirements:
3 years of marcom experience from a medical device company.
Building business plans and market analysis
Writing marketing materials
Developing and maintaining CRM programs
Producing and participating in conferences and exhibitions
Maintaining company website and social media assets
First degree (preferably from life science program)
Native-level English speaker. German and French a significant advantage.  
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experienced QA/RA professional 

  Li-Med - Asaf Azulay    Tel Aviv Area, Petach-Tikva   14/6/2016 
Category: QA - Quality Control, Biotechnology, Life Sciences, Medical Equipment, Regulatory Affairs, (, )  
Education: Masters   Position type: Full Time  Experience: 3 years 
Area(s) of expertise desired: GMP, Quality Assurance, Radiology, Regulatory Affairs  
Description:
We work with clients in the Medical Device field to build and implement their quality management system, as well as prepare regulatory strategy plans and files.  
Requirements:
B.A. in Mechanical Engineering/ Quality Engineering/ Biotechnology/ Life Sciences
2 years of experience with medical device Quality and Regulatory requirements (ISO13485, GMP)
Experience in writing and submitting regulatory documents for the European and American regulatory bodies
Experience with CE regulatory requirements
Has participated at least once in a CE quality/regulatory audit
Languages: proficient in Hebrew and English (reading, writing and speaking)  
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