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 179  View Titles Only  Page 1 of 18
 
Title   Company Name     Location   Date  
Very capable High-tech Medical equipment Marketing Representatives 

  Yaad Center    All, Haifa/ Tel-aviv   23/7/2007 
Category: Management/Executive, Medical Equipment, Sales/Marketing  
Education: Bachelors   Position type: Full Time  Experience: No experiece 
Area(s) of expertise desired: Academic, Business Analyst, Business Development, Executive, Finance, Investor Relations, Legal, Marketing, Medical Tech, Sales  
Description:

Very capable High-tech Medical equipment Marketing Representatives - for a very interesting and chalanging position.
 
Requirements:
No marketing experience is required !!!

Bachelor's degree in Law or Economics mandatory.

Master`s degree in Business an advantage.

Three years of work experience

Business orientation

Credibility and very good skills in comunication





 
To submit your resume , please sign in...
 
Postdoc and Ph.D. positions available 

  Volcani Institute    Tel Aviv Area, Rishon Le Zion   5/6/2016 
Category: Chemistry  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired:  
Description:
We have open postdocs and Ph.D. positions in our successful, interdisciplinary and dynamic laboratory at the Volcani Institute

Research areas
- Nanomaterials - Precise delivery systems
- Smart polymers - Natural polymers' chemistry
Requirements
- M.Sc. (Ph.D. for postdocs) in Chemistry / Chemical engineering / Materials Science
- Research experience with polymers / nanomaterials / materials chemistry is an advantage

Appropriate candidates will enjoy excellent conditions and fellowships
Different projects integrate academic research as well as industrial collaboration opportunities

For applications, please send your CV to Elena Poverenov elenap@volcani.agri.gov.il
Webpage: http://www.agri.gov.il/en/people/1024.aspx Tel: 03-9683354
 
Requirements:
We have open postdocs and Ph.D. positions in our successful, interdisciplinary and dynamic laboratory at the Volcani Institute

Research areas
- Nanomaterials - Precise delivery systems
- Smart polymers - Natural polymers' chemistry
Requirements
- M.Sc. (Ph.D. for postdocs) in Chemistry / Chemical engineering / Materials Science
- Research experience with polymers / nanomaterials / materials chemistry is an advantage

Appropriate candidates will enjoy excellent conditions and fellowships
Different projects integrate academic research as well as industrial collaboration opportunities

For applications, please send your CV to Elena Poverenov elenap@volcani.agri.gov.il
Webpage: http://www.agri.gov.il/en/people/1024.aspx Tel: 03-9683354
 
To submit your resume , please sign in...
 
Scientist, Formulation of Biologics 

  virdisPharma    Worldwide, Paris   28/4/2008 
Category: Biotechnology, Engineering, Life Sciences  
Education: Bachelors   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Formulation, Protein Chemistry, Proteomics, Research, Biologics  
Description:
Our client is a global biopharmaceutical company who is looking for Scientist in the Formulation of Biologics.
The appointed candidate will be Responsible for Pre-Formulation activities and Formulation Development of new biological entities.

Duties:
*Design and screening of protein formulation candidates
*Protein stabilisation studies
*Formulation optimization of biotherapeutics
*Process design and Scale up
*Responsible for running benchtop, pilot and manufacturing scale-up.

Other responsibilities:
*Technology transfer of drug product formulation and process to cGMP manufacturing team up to Industrial Affairs.
*Represent the department within project teams.
*Collaborate with other operating units within and outside the department (e.g. Discovery, Analytical, Chemistry,)
*Supply all the supportive documentation for CMC Regulatory documents.
 
Requirements:
The candidate will have experience in protein formulation (liquid and lyophilisation), Protein degradation pathways and Protein characterization methods (HPLC, SDS-PAGE, Biophysical methods)

They will also have,

*A degree in Pharmaceutical Science, Biochemistry, Chemical Engineering, Analytical Chemistry or related scientific field is required.
*Educated ideally to PhD level.
*Experience in formulation, process and dosage form development for biotechnology derived drug products for administration by various routes.
*Experience in parenteral liquid products,aseptic process and lyophilized protein development would be valued.
*Good understanding of analytical tools ( protein characterization, ).
*People management and team player skills.
*Must be able to communicate effectively in a cross-functional team environment (written / verbal).
*Excellent command of English, spoken and written.  
To submit your resume , please sign in...
 
Senior Director of Clinical Development 

  Verna scientific    All, mountain view, CA   19/1/2007 
Category: Life Sciences  
Education: Doctorate   Position type: Full Time Employee  Experience: 5 years 
Area(s) of expertise desired: Biochemistry, Bioinformatics, Biology, Biophysics, Biostatistics, Pharmacokinetics, Pharmacology  
Description:
Responsible for all medical aspects, medical monitoring, meeting Regulatory Authority requirements, develops clinical protocols, publish, manages CRO staff, Drug Safety Service/Global Pharmacovigilance Department, Post Marketing Surveillance campaigns, interfacing with sites, vendors, investors, collaborators, customers, Regulatory Authorities and Board of Directors.

supervises biostatistical support, Clinical Program Managers (CPMs) & Clinical Research Associates (CRAs) and other clinical staff.

Acts as safety monitor for all clinical programs.

Plans and builds fully integrated Drug Safety Service (Pharmacovigilance) for products marketed or co-marketed.

Responsible for oversight of all clinical safety reports and updates to all regulatory authorities and IRBs/IECs, as well as Annual IND updates, IB revisions, protocol (safety) amendmentsl, and input to ISS (ISEs) for NDAs.
 
Requirements:
Education: MD degree is required with Minimum 5 years of experience in clinical development and all aspect of clinical trials.  
To submit your resume , please sign in...
 
SAS Programmer 

  Verna scientific    North Area, Jersey City   11/6/2007 
Category: QA - Quality Control  
Education: Bachelors   Position type: Full Time Employee  Experience: 3 years 
Area(s) of expertise desired: Biostatistics, SAS  
Description:
Are you looking for professional growth opportunities as a full time employee enjoying OUTSTANDING BENEFITS? Do you have 1-4 years of professional experience in the biotech/pharmaceutical industry? We offer a rare opportunity to work within an organization where individual contribution makes a significant difference.

What Youll be Doing:

1-4 years of pharmaceutical/CRO experience as a SAS programmer

- Degree in Statistics or related field

- Phase II-IV clinical trial experience

- Safety and some efficacy experience

- Good understanding of the clinical process

- Good understanding of important study documents (e.g. Protocol, Case Report Forms, Statistical Analysis Plan)

- Good communication skills

- Any additional qualifications will be considered a plus (e.g. integration experience, handling FDA and marketing requests)

How to Reply

The most effective way of communication is via email please forward us your updated WORD FORMAT resume (Address, Contact number and email is must) Please mention your best hourly rate, availability and visa status. Any questions, do feel free to email us
to bob.harold@vernascientific.com

No Time to send out your Resume? Current Employed but Still Looking for a New Job? Just send your contact details and let our recruiters contact you
 
Requirements:
Minimum of 1-4 year pharmaceutical/CRO experience as a SAS programmer  
To submit your resume , please sign in...
 
Statistician - Validation/Process 

  Verna scientific    All, Swiftwater   6/6/2007 
Category: perm  
Education: Masters   Position type: Full Time  Experience: 3 years 
Area(s) of expertise desired: GLP, GMP, Laboratory, Quality Control, Validation  
Description:
Responsible for providing statistical support for validation, qualification, and comparability experiments, as well as performing data analysis upon protocol execution. Will support QC in method trending and provide statistical support for laboratory investigations as needed.  
Requirements:
We are an equal opportunity employer M/F/D/V Education/Years Experience/Other Skills : MS in Statistics, Minimum 3-5 years related experience in GxP environment
Requires cGMP/cGLP training and strong writing skills along with excellent statistical, analytical and computer skills.
 
To submit your resume , please sign in...
 
Statistical (SAS) Programmer 

  Verna scientific    All, Irvine   28/6/2007 
Category: Life Sciences  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired: Biostatistics, GLP, GMP  
Description:
Urgent requirement for one of the our top client located in 'CA.

Position Description:

This position will provide statistical programming support under the direction of the senior staff for the creation, quality control, documentation and maintenances of analysis data set, tables, listings and graphs.  
Requirements:
Requirements:

Education or education/experience combination equivalent to a post graduate degree in Computer Science, Life Science, Statistics or Statistic related field. One (1) years of pharmaceutical clinical research experience with Masters degree or Masters equivalent, or two (2) years of pharmaceutical clinical experience with a Bachelors degree or Bachelors degree equivalent.
General knowledge of medical terminology and clinical trial methodologies
Working knowledge of Base SAS, SAS/STAT; SAS Macro language a plus
Good analytical and problem solving skills
Excellent English communication skills (verbal and written) as well as good interpersonal skills
Focused, well organized, detail-oriented
Works well under pressure, with initiative to take on unfamiliar tasks.
Works well in a team environment.

Contact:

The most effective way of communication is via email please forward us your updated WORD FORMAT resume (Address, Contact number and email is must) Please mention your best hourly rate, availability and visa status. Any questions, do feel free to email us to bob.harold@vernascientific.com  
To submit your resume , please sign in...
 
Level II Source Inspection 

  Verify, Inc.    North Area, Haifa & Nazareth   5/1/2009 
Category: QA - Quality Control  
Education:   Position type: Temporary Employee  Experience:  
Area(s) of expertise desired: Quality Assurance, Quality Control  
Description:
Contract position in Haifa and Nazareth. 40 hours p/week on an on-going basis. Pay per hour depends on candidate's skills and qualifications. Please see further details below. Candidate will be contracted through Verify, Inc., but the position is for General Dynamics Ordnance and Tactical Systems. Please call Michelle Katz at 203 638 6325 or e-mail to mkatz@vscnet.com.

Primary Duties: MUST BE US CITIZEN
Report on potential and actual process, product and schedule issues as they arise
Assess production readiness of the subcontractor(s) from material receipts through final USG approvals (Lot Acceptance Tests-(LAT), Ammunition Data Card (ADT), and DD 250); this includes materials availability (line of balance information), human resources, training, work loading and equipment status
Identify production risks and work with supplier(s) to develop risk mitigation plans (single point failures, automated systems, etc)
Aid in processing of all paperwork necessary to support production (ADC, DD250s and Bills of Lading)

Quality:
Provide source inspection/acceptance services for the first articles and lot acceptance tests at subcontractor facilities in accordance with the technical data package
Witness, approve, prepare and submit Product Acceptance Documentation (Inspection Records and Supporting Certifications) per the training and direction received from GD-OTS Quality Assurance Personnel. The documentation is to be submitted through the Subcontract Administrator
Monitor and recommend subcontractor improvements based on process audits, inspection results and delivery
Participate in testing and failure analysis, as required
Provide corrective action suggestions for process improvement at subcontractor facility based on performance and customer complaints
Provide support for GD-OTS executed process audits
Assist GD-OTS personnel with the review of Ammunition Data Cards (ADC) and Certificate of Conformance (C of Cs) prior to official submittal from subcontractor
Support quality system audit with GD-OTS personnel, as directed

Primary Products:
Links (connect the bullets to make an ammo belt for example when ammo is being fed into a machine gun, the bullets are connected by links)
Ammunition


 
Requirements:
 
To submit your resume , please sign in...
 
Development Lead 

  Vensica Medical    Tel Aviv Area, Givataim   16/8/2015 
Category: Engineering, Medical Equipment  
Education:   Position type: Full Time  Experience: 3 years 
Area(s) of expertise desired: Engineering, Start-Up  
Description:
Vensica Medical is a start-up developing a Revolutionary Needle-Free Way To Effectively Deliver Drugs To The Urinary Bladder based on therapeutic ultrasound.

We are looking for a talented and experienced engineer to lead the product development.

The position entails:

Product design and lead
Lab and para-clinical trials management
Model building
Managing sub-contractors
 
Requirements:
Mechanical / Bio-medical / Physics Engineer
At least 3 years of experience managing product development in a bio-medical company
Experience in project lead and lab management
Para-clinical trial experience
Familiar with development protocols, QA and POCs
Independent and Motivated  
To submit your resume , please sign in...
 
Work in Singapore 

  TWLink Technologies Pte Ltd    All   13/9/2007 
Category: job posting  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired: Cardiology, Career Planning/Placement, Genetics, Oncology, Pharmacology  
Description:
All the expertise areas listed below.  
Requirements:
Able to work in Singapore  
To submit your resume , please sign in...
 
View saved jobs  
 View Titles Only Page 1 of 18
 
 
מטפלת מאגר מטפלות לילדים , אופרייות לוח דרושים הגדול בישראל כולל אלפי הצעות עבודה
 

Copyright 2005-2018 Biotech Jobs in Israel