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 1 - 10 of 30  View Titles Only  Page 1 of 3
 
Title   Company Name     Location   Date  
Operation Deputy Manager 

  confidential    All, Rehovot   26/12/2011 
Category: Biotechnology, Engineering, Chemistry, Life Sciences,  
Education:   Position type: Full Time Team Leader  Experience:  
Area(s) of expertise desired:  
Description:
The position includes: production of company products
Maintaining and co-managing the pilot plant
Managing as well as " hand" working
the job is for Rehovot and Hedera  
Requirements:
Relevant education- Engineer/practical Engineering degree or technologist in the fields of Chemistry/food/ Biotech/engineering or first degree (Bsc) in Biotechnology
Ability for intensive and hard work and unusuall working times
wanted yet not obligated:
previous experience in producing of plant extracts; work with mechanical manufacturing devices, such as centrifuges; reactors; filtration equipment and clean room work
background and experience in food or biotechnology industry  
To submit your resume , please sign in...
 
Clinical Research Associate/Senior Clinical research associate- office/home based 

  Hays Pharma    All, Izrael (anywhere)   6/11/2007 
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 Employee  Experience: 2 years 
Area(s) of expertise desired: Clinical Research  
Description:
JOB FUNCTIONS/RESPONSIBILITIES:

Recruitment of investigators.
Co-ordinate all the necessary activities required to set up and monitor a study, including the following:
Identify investigators
Help, when requested, in preparation of regulatory submissions
Design patient information sheets and consent forms.
Ensure timely submission of protocol/consent documents for ethics/IRB approval.
Placement and initiation visits.
Conduct regular monitoring visits in accordance with site monitoring SOP / Sponsor site monitoring SOP, as appropriate
Maintain all files and documentation pertaining to studies.
Motivate investigators in order to achieve recruitment targets.
Complete accurate study status reports.
Ensure the correct storage of drugs and the diligent account of all drugs in accordance with SOPs.
Keep the project manager informed.
Process case record forms to the required quality standards and timelines.
Deal with Sponsor generated queries in a timely manner.
Ensure the satisfactory close-out of investigator sites.
Participate, if requested, in the preparation of and review of study documentation, e.g. draft protocols, draft CRFs, monitoring guidelines and elements of final report.
Ensure correct archiving of files on completion of a study.
Co-operate with sponsor and/or QA personnel in the conduct of QA audits.
Maintain patient and sponsor confidentiality.

 
Requirements:
Cost effectiveness.

To participate in training new staff as appropriate.

Assist with marketing the company if and when appropriate.



QUALIFICATIONS/EXPERIENCE REQUIRED:

Medical/science background and relevant experience.

Ability and willingness to travel at least 50% of the time.(lnternational and domestic: fly and drive).

Ability to review and evaluate clinical data.

Computer literacy desirable.

Foreign language skills desirable.

Current full driving licence essential.

Good oral and written communication skills.



 
To submit your resume , please sign in...
 
management 

  MECO IND    All, new york   15/10/2007 
Category: Chemistry  
Education:   Position type: Full Time Employee  Experience:  
Area(s) of expertise desired: Administration  
Description:
kidjirourirhujfririeioeikjfufiriiodjkdjfdidikdjkifjfjfjfjfjfncnvbvnvmkdksowowowieuryrjfjfjhfhjdmxnxbcbcbvnmxkwkwiwi  
Requirements:
iwiuejhhfgfhjdksowowieiruryuyhfhfjdfncnvnbvncmckxkswowiuruyruyrudjdjfhfghfjdkdkwowowowieuiruruhfjfjfdjdjd  
To submit your resume , please sign in...
 
Manufacturing 

  Fellen Project    All   2/8/2007 
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: Masters   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Manufacturing/Production  
Description:
Our client, a manufacturing company. has an immediate opening for cost accountant with 4-year accounting degree and a minimum of 2-4 years experience in a manufacturing process cost environment. Responsibilities include preparation of manufacturing budgets, month-end close, standard cost and variance analysis, financial analysis, and inventory reconciliation. The successful candidate should have the ability to work with various levels of management and a working knowledge of Microsoft Excel. JD Edwards or other MRP package experience preferred. Salary 45-55K. DOE  
Requirements:
Our client, a manufacturing company. has an immediate opening for cost accountant with 4-year accounting degree and a minimum of 2-4 years experience in a manufacturing process cost environment. Responsibilities include preparation of manufacturing budgets, month-end close, standard cost and variance analysis, financial analysis, and inventory reconciliation. The successful candidate should have the ability to work with various levels of management and a working knowledge of Microsoft Excel. JD Edwards or other MRP package experience preferred. Salary 45-55K. DOE  
To submit your resume , please sign in...
 
manager 

  Kristin Burrows investments    All, waterford   30/7/2007 
Category: Chemistry  
Education: Masters   Position type: Full Time Manager  Experience: 9 years 
Area(s) of expertise desired: Administration, Human Resources  
Description:
y rj,he j. fd ihldfz hlf dz hdz hd.z fdz hjfdz. fdz hj.fkdz hjfkd.z hjfd.z fdz jd jd.z k. hkdz l.bdz gdz hkgdz lg.l hkg ldl gz. khdz k.fdzh k.d.k hdzf hk.dzf. hkdz .jdz. jkdz. hkzd. hkdzf. hkzd. hjgdz jdz hjdz hjgd.z. khzd. jz. hkdz. hkjdz. hjkd. jgdz. hjkgdzj h,dz. hkdz. hdz. dz. hkdzg hj.kzkjzd. hjkdz hjdz kj.dz hjd.z lkdz lhkd. .ldz .hdzzj k.lhdz jgd.z hjgd.z hj.fkdz. hjfdz hjfd.zh j.kzzfd h.df hjf. hj.fdz hjfkd.z hjfd.z .hfdz lfdz hfdzld.z lkhdz lkzfd l.fdzl hdz l.fdz l.fdz l.fdz lfdz hddl khf lkhdfl fdz lkjdzl khdzl . hd.l hk.f h hkfd h.hlkd  
Requirements:
oh i.e shil. li dzlhi dzlz dk j.df z kj.dz kj.dfz hlk.dfzk j.dfz hljdfz kj.zd hj.dzf lh.dzf lhkdfz lhkdz lhkdz lhdz lhkdz ldz lhkzd ldzf hlkdzf lhdz hjdl ldz hldz lhkdzf lhkdz lkjdz lkdz lhkdz lkdz hjd lhkdz hlzd hldz hldfz hldzf hldfz hldfz hldfz hldfz lhdfz hldfz hljdzf hldfz lhdzf lhdzf lhdzf lhzd jk.dz lhkdfz lh dz lfdz lhkzdf lidzf lhdzf lhkfdz lhdzf lhkdz hlkfdz hlkfdz lfdz lfdz hljfzd lhfdz hjlzd jlzdf hlfdz hdzf hlzfd hlkdzf hldfzl hdfz lkfdz lhdfz hldzf lkdfz lfdz hldfz lhfdz hlfdz lfdz lkfdz lfdz hlfdz klfdz hlkfdz lkfdz hkl fdz hlkjfdzj lfdzk lfdz lkd lk fdz lkfdz lkdfzl kzdk ldfzl kdfzl kdzfl dzf kldzf kldfz lhdz kjldzf lkhdfzk ldz kldzf lzdf lkz lkzd lkz lkz lkz lkz d lkzlkjz klzdlkzlkzd lkzd lkzd lkzd klhzd lkzfd lkz lkzfdk lzfdk lzfd kjlfzdl kfzd lkfdz lkfzdl kfzd lkfdz lkzfd klfzdl kfdz klfzd kldzfk lfdzkl fdzkl fdz lkdfz klfdzl kfdz ldzf lkfdzk lfdzl kfdz kldfzl kdzf lkfdz klzd klzfdl kz df lkzfdl kzdfl kzdfl dzf lfzd lfdz lkfdz lkdzf lkzdf lkdfz lkd zf lkdzk lzdk ldzl kdzf lkdzfl dzf lkdzf lkfdz lkdzfl kdzf lkfdz lkdz lkdzf lkdzf ldzk l kl lk kld kldfz kldfz klfdz lkdfl kfdz ldk lk l f  
To submit your resume , please sign in...
 
CRA II 

  Hays Pharma    All   13/7/2007 
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 Employee  Experience: 2 years 
Area(s) of expertise desired: Clinical Data Management, Clinical Research  
Description:
Our client, a worldwide Contract Research Organization, is seeking for its branch in Milan a Senior CRA to Identify, select, initiate, and close-out appropriate investigational sites for clinical studies. Monitor those sites in order to ensure that studies are carried out according to the study protocol, SOPs/WPs, applicable regulations and the principles of ICH-GCP. Depending upon experience, become involved, when required, in other areas of study management and staff training and contribute to the review of the Company"s systems and procedures as appropriate. Provide a benchmark of monitoring competence to inexperienced/less experienced colleagues and acting according to Company"s values and as a positive promoter.

 
Requirements:
For this role is required significant experience as a CRA for at least 18 months.

This is for an international company- please provide all CV's in English format
Thankyou  
To submit your resume , please sign in...
 
Clinical Project Manager 

  Hays Pharma    All   10/7/2007 
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  Experience: 4 years 
Area(s) of expertise desired: Clinical Research  
Description:
Managing all aspects of studies or study programmes allocated by the GM or SPM and to be responsible for ensuring control of allocated study budget.

 
Requirements:
Responsibilities include:

To participate in the preparation of clinical development plans
To manage clinical studies
To ensure that studies are performed and completed in accordance with the pre-defined budget, timelines and quality specifications
To participate in CRO evaluation and selection and be responsible for making selection recommendations to SPM/DGM
To coordinate the establishment of service provider contracts.
To ensure that a safety reporting system is in place and that safety reports are provided to the Safety Department in a time manner
To ensure that studies are conducted in accordance with EU GCP requirements and relevant company SOPs
To produce or co-ordinate the preparation of study protocols  
To submit your resume , please sign in...
 
Extra Money in a new Sales Project 

  Con    All   23/5/2012 
Category: Biotechnology, Chemistry, Life Sciences, Pharmacy/Pharmacology, Healthcare, Sales/Marketing  
Education:   Position type: Full Time Employee  Experience: No experiece 
Area(s) of expertise desired:  
Description:
International nutrition company is looking for 5 new employees to join a dynamic sales team.
Challenging job in marketing & sales.
Min 10 hrs/week.
Extra 2000-4000 nis (predictable income)
Option to work from home.
Please send CV to: project@slimail.com  
Requirements:
Please send CV to: project@slimail.com  
To submit your resume , please sign in...
 
Job Offer in UK 

  LSC & Construction Engineer Ltd    All   28/6/2013 
Category: Engineering, Chemistry, Clerical/Administrative, Pharmacy/Pharmacology  
Education: Masters   Position type: Part Time  Experience: 3 years 
Area(s) of expertise desired:  
Description:
Engineers, Foremen, Captain, Mate Engineer, 2nd Engineer, 2nd/3rd Officer, Deckhand, Steward, Chef, Seafarers , Crew Job Seekers , Chief Engineer , Doctors, Nurses, Laborers, Pharmacists, Dentists, Masons, Plumbers, Drivers, Heavy equipment operators, architects, Surveyors, Customer Care Representatives.  
Requirements:
Certificates required  
To submit your resume , please sign in...
 
Clinical Research Associate II 

  Hays Pharma    All   10/7/2007 
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: 2 years 
Area(s) of expertise desired: Clinical Data Management, Clinical Research, Regulatory Affairs  
Description:
My client, a global leading organisation within the pharmaceutical industry, is presently seeking a Senior CRA to work over in Berkshire.

My client is looking for candidates to perform trial initiation, monitoring and close out activities in Phase II-IV clinical research, managing study site activities to ensure clinical data integrity in line with company and regulatory guidelines, and providing clinical and technical support to other CRAs and administrative staff.

As Senior CRA you will provide clinical and technical support, conduct co-monitoring/training visits and assist with protocol review, CRF and informed consent development, plus study start up activities. Where required, you will be the primary client contact for project related activities, and also act as mentor for CRAs.

 
Requirements:
Reporting to project leader, you may assume the role of a Lead CRA on projects by providing direction to the project team, coordinating monitoring activities, developing CRFs and acting as liaison between monitoring and other functions.  
To submit your resume , please sign in...
 
View saved jobs  
 View Titles Only Page 1 of 3
 
 
מטפלת מאגר מטפלות לילדים , אופרייות לוח דרושים הגדול בישראל כולל אלפי הצעות עבודה
 

Copyright 2005-2018 Biotech Jobs in Israel