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Trendlines Group 
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Job Search Results: Jobs 1 - 2 of 2  View Titles Only  Page 1 of 1
Title   Company Name     Location   Date  
Lead Scientist 

  Trendlines Group    Tel Aviv Area   8/5/2017 
Category: Life Sciences  
Education: Doctorate   Position type: Full Time  Experience: 4 years 
Area(s) of expertise desired: Academic, Biochemistry, Biology, Immunology, Molecular Biology, Protein Chemistry  
An agtech company in the plant protection sector is looking for a Lead Scientist (Doctoral degree with several years of post-doctoral experience).
Primary Responsibilities
The qualified candidate is responsible for contributing intellectual and experimental knowledge to the strategic development of the company.
•Design and implement a screening cascade using an antibody platform to key drugable targets
•Optimize protein expression and purification scheme of lead candidates to ensure maximal protein quality
•Design strategic experiments to address critical scientific questions
•Identify, assist and/or lead external collaborations
•Ability to perform protein/antibody engineering
•Manage team members and subcontractors  
•Ph.D. in molecular biology, biochemistry, bioengineering, immunology or related discipline with a minimum of 4 years of postdoctoral experience
•Experience in industry
•Experience in engineering and screening antibodies
•Experience with characterization of antibodies and proteins using a variety of biophysical and biochemical techniques
•Deep understanding of immunization strategies
•Proficient in transfection, expression and protein purification techniques
•Ability to take initiative and independence, together with a capacity for collaboration and team work
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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  
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 company’s processes and products are in compliance with applicable quality standards and requirements
•Establish quality assurance and quality control inspection and testing procedures
•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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מטפלת מאגר מטפלות לילדים , אופרייות לוח דרושים הגדול בישראל כולל אלפי הצעות עבודה

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