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Job Search Results: Jobs 11 - 20 of 30  View Titles Only  Page 2 of 3
 
Title   Company Name     Location   Date  
Clinical Application Development Scientist (position # 1296) o 

  Mengo    North Area, Yokneam   14/5/2010 
Category: Clinical Research, Medical Equipment  
Education:   Position type: Full Time  Experience: 4 years 
Area(s) of expertise desired: Clinical Research, Surgery  
Description:
Please send your resume in a .doc format to jobs2@mengo.co.il
You must indicate at the headline of your email the no. of the position 1296

Affiliation: reporting to the Medical Director

Job Description and Main Tasks:
Acquisition, analysis and reporting of application related technological, scientific and clinical data including and maintenance of a clinical and scientific database (scientific literature, internet, market reports, etc.).
Professional support of the Medical Director activities including: writing protocols, multi-centers studies, coordination with physicians, laboratories and hospitals, issuing reports, etc.
Writing reports for in-house and external purposes and preparing multimedia presentations.
Assisting in writing scientific papers.
Working closely with bodies within and outside the company including CROs, clinical monitors, MDs nurses, etc.
Active participation in the R&D Application Group activities.
 
Requirements:

Qualifications:
Academic M.Sc. or preferred Ph.D. in either: bio-medical engineering, medical science, biology, medicine (MD) or equivalent.
At least 5 year experience in a medical device company.
Mother tongue level English.
Ability to read and analyze high volumes of scientific data.
Journal level scientific papers writing capability.
Familiarity with operating rooms environment and equipment and with surgical procedures.
Familiarity with regulatory processes (FDA, CE, IRB) - advantage.
Reliability, team worker, excellent inter-personal relationships.


 
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Hardware developer Eng. 

  electronic    Tel Aviv Area, Petach-tikva   11/10/2009 
Category: Medical Equipment  
Education:   Position type: Full Time  Experience: 10+ years 
Area(s) of expertise desired:  
Description:
1. Over 45 years old
2. planning and creativity abilities
3. 12 years experiance in Electronic development
4. prefferable power suppliers and RF developers
5. Work place in Petah-Tikva
6. working hours 08:00-17:00 without Fridays  
Requirements:
 
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software engineer C++ 

  Mengo    Tel Aviv Area   16/7/2009 
Category: Engineering, Medical Equipment, IT/Hardware/Software  
Education: Bachelors   Position type: Full Time Employee  Experience: 5 years 
Area(s) of expertise desired: Academic, Other, Software Development, , software  
Description:
 
Requirements:
 
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Software / Image processing engineer 

  Confidential    Tel Aviv Area   8/6/2009 
Category: Medical Equipment, IT/Hardware/Software  
Education: Bachelors   Position type: Full Time  Experience: 3 years 
Area(s) of expertise desired: Software Development, Image processing  
Description:
Medical Imaging product development experience in image processing.
Design and develop concepts for new algorithms. Design and implemention of GUI. Debugging and system integration. Interact with customers  
Requirements:
3+ years experienced with C/C++.
Strong understanding of Object Oriented Design (OOD) and Programming (OOP).
Extensive knowledge experience in one of the following: Image Processing/Image recognition processing - preferred.
Oral and written communication skills in English Must.
Strong problem solving and troubleshooting skills.
Ability to work in a team, ability to work independently.
Commitment to work plans and schedules.
Creativity, Self learner, Quick learner.

Education
Masters/Bachelor degree in engineering (Computer, Electronics).  
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VP/ Director RA / QA 

  Mengo    All   8/5/2009 
Category: QA - Quality Control, Biotechnology, Pharmacy/Pharmacology, Medical Equipment, Regulatory Affairs  
Education:   Position type: Full Time Executive  Experience:  
Area(s) of expertise desired: Medical Device, Pharmacology, Quality Assurance, Regulatory Affairs  
Description:
Responsibilities:

1. To establish, maintain and improve the quality system in accordance with 21CFR820, ISO9001 and ISO13485
2. To act as the management representative as defined in the quality system responsible for:
ensuring that quality system requirements are effectively established and maintained; and
reporting the performance of the quality system to senior management for review

3. To manage the following quality system processes to ensure compliance with the applicable regulations, standards and directives including:
Documentation control, auditing, training, management review, complaints, product quality acceptance, supplier control, change control and quality planning.

4. Assist with the preparation, filing, and negotiation of submissions to regulatory bodies to obtain market or clinical research approvals including ongoing trials and post-approval activities.
5. Review clinical trial documents including clinical protocols/reports, investigator brochures, nonclinical reports, CMC protocols/test methods;
6. Reviews labeling, promotional material, product changes and documentation for changes requiring government approval
7. Monitor changes to domestic and international regulations and standards and ensure compliance with those regulations and standards
 
Requirements:
Qualifications:

** More than 10 years experience in the Biopharmaceutical or Medical Device industries.
**At least 5 years management experience in Quality assurance and Regulation in Biopharmaceutical or Medical Device industries.
** Experience with Notified Bodies in Europe.
** Experience with quality requirements for clean rooms and sterilization

 
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VP Marketing & Sales 

  L-IL - Top Talent Acquisition    Tel Aviv Area   27/2/2009 
Category: Biotechnology, Medical Equipment  
Education:   Position type: Full Time  Experience: 7 years 
Area(s) of expertise desired:  
Description:
Building a marketing strategy, closing agreements, locating and managing international distributors.  
Requirements:
MBA in Business Administration/ Economic/Life Science
Former positions as VP Marketing & Sales
Proven experience in managing international Marketing & Sales in bio companies
Tele-Medical/ Distress buttons/ Medical Device/ Elderly field experience
Experience in locating and managing international distributors
Excellent familiarity with US and Europe regulation and territories
Experience in Hi Tech / biotech Companies
Presentation skills
English as mother tongue
Experience in living and working in the US
 
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R&D Manager for a drug delivery biotech startup company 

  Confidential    Tel Aviv Area   9/2/2009 
Category: Medical Equipment  
Education:   Position type: Full Time Manager  Experience:  
Area(s) of expertise desired:  
Description:
 
Requirements:
 
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CRA 

  Hays Pharma    Tel Aviv Area   4/11/2008 
Category: QA - Quality Control, Biotechnology, Engineering, Chemistry, Life Sciences, Clinical Research, Clerical/Administrative, Management/Executive, Medical Management, Pharmacy/Pharmacology, Medical Equipment, Regulatory Affairs, Healthcare, Sales/Marketing, IT/Hardware/Software  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired:  
Description:
Our client, a global CRO is looking for Clinical Research Associates with minimum 1 year of experience join a professional team.

The responsibility of a Clinical Research Associate II (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with companys SOPs. As Regional CRA or Primary CRA (on smaller studies) responsibilities will include managing clinical monitoring activities in addition to the ownership of investigator sites, including investigator/site selection, collating regulatory documentation, initiation and monitoring (source data verification, drug accountability and data collection) in accordance with ICH GCP guidelines.

Responsibilities

Perform clinical trial initiation, monitoring and closeout activities.
Assists with study start-up activities, site selection, and pre-study activities to identify and evaluate potential investigators.
Assists in site evaluation and reports to Lead CRA / Project Leader as appropriate.
Assists in submission of documents to the Ethics Committees, when required.
Participates in study specific training.
Assists with the preparation and coordination of investigator meetings and attends meeting.
Provide status updates of pre-study and initiation activities to Lead CRA / Project Leader.
Completes initiation visits with study staff through training, reviewing regulatory requirements, collecting outstanding documents, reviewing patient screening/randomization procedures, reviewing SAE reporting requirements, and reviewing drug storage and accountability procedures.
Assists in development of patient enrollment strategies with the project team and study site coordinator
Ensures proper storage, dispensation, and accountability of all Investigational Product(s) and trial-related materials.
Completes monitoring visits to ensure the integrity of clinical data and appropriate follow up procedures, including source document verification and SAE reporting in accordance with the project plan.
Manages study site activities and provides ongoing updates of site status to Lead CRA / Project Leader.
Maintains tracking records for assigned sites such as tracking of status and source document review per patient.
Completes study site closeout visits.
Assists with Project specific administrative activities as a member of the project team.
Ensures site registration in Investigator Database.
Increases knowledge of drug development process, therapeutic areas, Good Clinical Practices, and any applicable local regulatory requirements.

 
Requirements:


MD
Fluent official language of the country
English, written and spoken, upper intermediate
PC user
 
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Medical Advisor-Greece 

  Hays Pharma    Worldwide   4/11/2008 
Category: QA - Quality Control, Biotechnology, Engineering, Chemistry, Life Sciences, Clinical Research, Clerical/Administrative, Management/Executive, Medical Management, Pharmacy/Pharmacology, Medical Equipment, Regulatory Affairs, Healthcare, Sales/Marketing, IT/Hardware/Software  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired:  
Description:
Medical Advisor opportunity has arisen within a blue-chip pharmaceutical company in Athens. This is a highly interactive role, demanding effective strategic thinking and planning skills and the ability to network, teamwork and build influential relationships with your colleagues, customers and external opinion formers.
As a Medical Advisor you will provide a specialist role in a number of therapeutic areas. You will work closely with your commercial colleagues to provide pro active input into the strategic management of the business, jointly agreeing, developing and implementing strategic direction within key therapeutic areas, allowing commercial aims and ambitions to be met.

The role requires a good understanding of clinical development processes and of the changing health care environment


Accountabilities

Providing authoritative opinion on medical, legal and regulatory matters to support your colleagues across the UK, enabling them to comply with the relevant statutory requirements (e.g. Code of Practice, Medicines Act, and EU Directives).
Provision of pro active input to the development of business strategy.
Effectively developing relationships with key influencers and external organizations to ensure that the company retains a leading voice in the pharmaceutical industry.

Coordinating and utilizing specialist knowledge with brand aligned colleagues in formulating and implementing short and long term medical strategy for optimal commercial benefit.
Working closely with regulatory, commercial and clinical colleagues on pre-launch planning, including strategic evidence planning and generation.
Influencing clinical research strategies in support of market needs
Provide medical information
Knowledge of the clinical practice, care pathways, key competitors, etc. and input where required into study allocation process.
Input into a development of local protocols, patient information customer-initiated research projects (CIRPs) and named patient programmes.
Input into reviews and sign off of abstracts, reports and publications.
Pro active input into European Medical meetings to ensure strategy is supported.
Review and sign-off Regulatory documents as required.

 
Requirements:
Qualifications/Experiences

A registered medical doctor.
Expert therapy knowledge in a broad range of therapeutic areas,
Continuous record of career achievement through clinical development and/or medical affairs positions.
Previous industry experience would be beneficial
A good understanding of the changing health care environment.

 
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R & D MANAGER 

  BINA HR CENTER    Sharon Area   12/8/2008 
Category: Engineering, Medical Equipment, IT/Hardware/Software  
Education:   Position type: Full Time Executive  Experience: 5 years 
Area(s) of expertise desired:  
Description:
WE NEED A R & D MANAGER  
Requirements:
Bsc in Electrical Engineering

Few years of experience in board design

Few years of experience in managing small projects with many point

of contacts

Few years of experience in working with micro-controllers, specifically ARM processors

Experience in working with sub-contractors, 3rd party companies and external consultants.

Good understanding of algorithmic design and digital design flows

Understanding of software methodologies

Ability to define requirements and derive specifications

Experience with real-time design - an advantage

Experience with bio-signal processing - an advantage
 
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