Jobs in biotechnology, pharmaceutical, medical devices and life sciences industries.
 
Find the right job
Enter keywords
Category
Location
Position type
Jobs posted within:
 
 
 
 
 

 
Job Search Results: Jobs 11 - 20 of 36  View Titles Only  Page 2 of 4
 
Title   Company Name     Location   Date  
CRA 

  Confidential    Sharon Area   12/1/2012 
Category: Life Sciences, Clinical Research, Pharmacy/Pharmacology, Medical Equipment  
Education: Masters   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Clinical Research  
Description:
 
Requirements:
 
To submit your resume , please sign in...
 
Clinical Research Physician 

  *****    Sharon Area   2/12/2011 
Category: Clinical Research, Management/Executive, Medical Management, Healthcare  
Education:   Position type: Full Time Manager  Experience: No experiece 
Area(s) of expertise desired: Academic, Internal Medicine, Oncology  
Description:


A leading international pharmaceutical company is seeking a Medical Doctor specializing in Oncology for the position of Clinical Research Physician. The CRP will manage medical domains, be responsible for the clinical studies, serve as professional authority supporting Marketing, and develop relations with opinion leaders.

 
Requirements:
An intern with sub-specialty in Oncology and experience in the Pharmaceutical Industry.

A medical graduate / Oncology specialist, experienced in the Pharmaceutical Industry will be considered too.

English fluent.

Analytic skills, presentation & communication skills.

 
To submit your resume , please sign in...
 
Study Coordinator 

  Psychiatry Clinic, Sheba Medical Center    Tel Aviv Area   11/7/2011 
Category: Clinical Research  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired: Clinical Research  
Description:
 
Requirements:
 
To submit your resume , please sign in...
 
Director, Manufacturing 

  Scientific Search    Worldwide   14/3/2011 
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  
Education: Bachelors   Position type: Full Time Manager  Experience: 10+ years 
Area(s) of expertise desired: Bioanalytical Services, Biology, Manufacturing/Production  
Description:
Summary
This position is responsible for the technical oversight of biomanufacturing activities at contract manufacturing organizations associated with the production of critical raw materials, Drug Substance and Drug Product.
Responsibilities
Execute on time and cost the Manufacturing Supply Forecasts through oversight of third party manufacturers based in Japan, Israel and the US : Act as Person in Plant during manufacturing campaigns
Conduct technical audits of manufacturing operations to identify opportunities for Continuous Improvement at third party manufacturers
Technical review of batch documents
Trouble shoot manufacturing issues and support QA in Deviation and CAPA activities
Support QA in the technical review of Change Requests
Assist the Chief Technology Officer in the development of budgets
Provide data to populate the KPI program for Manufacturing
Other projects and assignments as required.
 
Requirements:
Requirements
BS Degree, in either bioengineering or a biological science.
Fifteen-plus years experience in manufacturing of biological products
Five-plus years in the management of biopharmaceutical manufacturing operations.
Excellent communication skills in Hebrew, both oral and written.
Profound knowledge of GMP requirements associated in biomanufacturing in the US and Internationally.
Knowledge of the engineering aspects of biopharmacecutical manufacturing plants
Experience working with CMO's
Goal oriented with a problem solving mindset
Proficiency with computers and major software packages, e.g. Microsoft Excel, Outlook, Powerpoint, Project
Excellent communication skills in English, both oral and written.
Travel - 25%
 
To submit your resume , please sign in...
 
Junior Sales Representative Surgical 

  Covidien    Tel Aviv Area, Tel Aviv   27/12/2010 
Category: QA - Quality Control, Biotechnology, Engineering, Chemistry, Clinical Research, Clerical/Administrative, Management/Executive, Medical Management, Pharmacy/Pharmacology, Medical Equipment, Regulatory Affairs, Healthcare, Sales/Marketing  
Education: Bachelors   Position type: Full Time  Experience: 3 years 
Area(s) of expertise desired: Medical Affairs, Medical Device, Sales  
Description:


Position: Junior Sales Representative Surgical (3)
Location: Central Israel (Tel Aviv)

Covidien

It's a new era with nothing but promise. Today, Covidien is more than a leading provider of medical devices, supplies and pharmaceuticals. Were a $10 billion company with over 40,000 employees who are passionate about helping doctors, nurses, and other medical industry professionals to as effective they can be.
A company with a true global mindset, Covidien has forged dynamic partnerships with medical professionals around the world. In our role as an integral collaborator, we help identify patient needs and translate them into proven procedures and products that improve and save lives.

As a Junior Sales Representative Surgical focused on our prestigious products, you will work closely with doctors, surgeons and specialist groups, selling into hospitals and a variety of practices across the centre of Israel and Central region - Jerusalem.
In return, we will provide you with world-class training, frequent development opportunities, rewarding benefits and the opportunity to work in a varied, challenging role with a large scope for demonstrating your independence, innovation and your talent for sales.

As a Junior Sales Representative your main responsibilities will involve:

Selling a portfolio of world renewed Surgical products across your established customer base
Increasing sales in line with agreed budgets
Building on well established relationships, to become an expert advisor to healthcare professionals
Being resilient, a strong negotiator and advocate for your products whilst identifying new opportunities in your market place
Cooperating with Customer Service Department
Participating in preparation and monitoring outcome of tender offers within the territory

 
Requirements:
As a Junior Sales Representative your skills and qualifications will ideally include:

Comprehensive selling experience B2B business (preferably in medical environment)
Previous sales experience or the desire to develop your sales ability
Good command of English to business standard
A full clean Driving License

What we will be looking for in you:

This role will suit a performance-driven young individual who enjoys working in a competitive environment and seizes the opportunity to get the awards that over-achievement brings. Ideally, youll have excellent presentation and negotiation skills and genuinely enjoy building long-term, trusting relationships with your customers.

Contact:

To apply follow the link:
http://www.tycohealthcarecareers.com/tycohcinternational/jobboard/NewCandidateExt.aspx?__JobID 9449

 
To submit your resume , please sign in...
 
Assistant VP RA/QA 

  Mengo    North Area, Cessaria   17/10/2010 
Category: Clinical Research, Regulatory Affairs  
Education:   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Clinical Data Management, Clinical Research, Quality Assurance, Regulatory Affairs  
Description:

i. Assist VP RA/QA in the following:
1. Manage the informed consent document
2. Manage safety reporting
3. Assist in the preparation of documentation for the study approval and running phases (submissions, responses to regulatory authorities, investigator brochure, progress/annual reports, amendments etc)
4. Maintain Company's Document Control center  
Requirements:
Assist Clinical Quality Manager in the following:
1. Assist Clinical Trial Managers in maintaining in-house study binders
2. Review monitoring reports
3. Assist in follow up of post audit CAPA
4. Review protocol deviations
iii. Israel CRA
1. Perform monitoring trial activities in the local Israeli sites
2. Experience/Skills Required
a. 2-3 years minimum work experience as a CRA
b. High level of English writing skills
c. Experience preparing informed consents and other clinical study related documentation (investigator brochure, progress/annual reports etc)
d. Excellent communication, organizational and recordkeeping skills required
e. Must be able to work in a fast-paced environment with demonstrated ability to juggle multiple competing tasks and demands

3. Required Education
a. Formal CRA training (e.g. BioForum CRA course or in-house CRO courses)
b. Bachelors degree in life science-related field
c. Related degree with an equivalent combination of education and experience will be con
 
To submit your resume , please sign in...
 
Applications Development Engineer (position # 1213) o 

  Mengo    North Area, Yokneam   14/5/2010 
Category: Clinical Research  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired:  
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 1213


Duties & Responsibilities:
Responsible for all operational aspects of pre and clinical trials including all related logistics, communication and coordination with the operating room staff.
Budget, follow up and control of project plans
Managing the technology and clinical databases at DHF standards.
Take active part in integrating technological solutions into the product/application being developed.
Managing tasks with external organizations and staff (e.g. hospitals, labs, suppliers).
Testing of prototypes for clinical performance and engineering evaluation.
Responsible for managing all stages of pre and clinical trials from design to final report including procedural monitoring and documentation (protocols, instruments and accessories order, sterilization etc).
Follow PDI processes related to product definition to release.
 
Requirements:
Academic B.Sc. or preferred M.Sc in either: bio-medical engineering, medical science, medicine (MD) or similar.
At least 3 year experience in a medical device company.
Ability to design and support clinical trials as well as to execute technical tests (protocols, implementation, reports).
Good technical capabilities and creativity.
Familiarity with operating rooms environment and equipment and with surgical procedures - advantage.

Personal
English fluent talking and high level writing - mandatory.
Quick learning curve.
High diligence.
Assertive.
High pressure and workload capabilities.
Teamwork oriented.
 
To submit your resume , please sign in...
 
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.


 
To submit your resume , please sign in...
 
Regulation of drug development 

  ISK Ltd    Jerusalem Area, Jerusalem   21/12/2009 
Category: Life Sciences, Clinical Research, Pharmacy/Pharmacology  
Education: Masters   Position type: Part Time  Experience: 1 year 
Area(s) of expertise desired: Clinical Research, Formulation, GLP, GMP, Pharmacokinetics, Pharmacology, Safety, Toxicology  
Description:
b"h

our company is engaged with anti cancer drug development and we are looking for a part time employee to be resposible for the regulatory affairs of the company BUT not a consultant  
Requirements:
b"h




we ask a regulatory person with 1-2 years of experience of work in the field that can work with our regulatory consultant  
To submit your resume , please sign in...
 
CEO is needed for a pharmaceutical company 

  Mengo    Jerusalem Area, jerusalem   23/9/2009 
Category: Biotechnology, Clinical Research, Management/Executive, Pharmacy/Pharmacology, "  
Education: MBA   Position type: Full Time Executive  Experience:  
Area(s) of expertise desired: Executive, Oncology, "/CEO  
Description:
Experience with accompanying Clinical Trials in the field drugs , preferably oncology drugs .


Experience in Business Development.


Experience from a startup company and preferably from a public company.


Experience with raising capital - as advantage.


The role includes travelling abroad.
 
Requirements:
Experience with accompanying Clinical Trials in the field drugs , preferably oncology drugs .


Experience in Business Development.


Experience from a startup company and preferably from a public company.


Experience with raising capital - as advantage.


The role includes travelling abroad.
 
To submit your resume , please sign in...
 
View saved jobs  
 View Titles Only Page 2 of 4
 
 
מטפלת מאגר מטפלות לילדים , אופרייות לוח דרושים הגדול בישראל כולל אלפי הצעות עבודה
 

Copyright 2005-2018 Biotech Jobs in Israel