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Job Search Results: Jobs 11 - 20 of 26  View Titles Only  Page 2 of 3
 
Title   Company Name     Location   Date  
Key account manager - custom synthesis 

  Novetide    Worldwide, North   24/6/2010 
Category: Biotechnology, Chemistry, Pharmacy/Pharmacology, Sales/Marketing  
Education:   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired:  
Description:
* Generating new business in the assigned field
* Developing current and future business to ensure growth in all revenue streams by building and leveraging a network of executive ationships with key customers
* Simultaneously managing a substantial number of accounts, being responsible for all revenue otas and forecasts
* Maintaining and documenting accurate,timely forecasts of opportunities, providing appropriate updates to executive management and providing timely updates with accurate customer and pipeline information
* Define product strategy and roadmap, develop and implement a company plans.
* Specifying and prioritizing roduct and customer requirements
* Act as a contact person to R&D and manufacturing experts
* Manage product documentation
* Gain knowledge with respect to the competition in the field
* Perform product service to customers
* Manage customer contacts throughout product life cycle (sales opportunities, customer needs, customer complaints, etc.)  
Requirements:
Capabilities:
1.knowledge and experience in marketing and sales
2.Pharmaceutical knowledge, understanding of API business an advantage
3.Strong negotiation skills
4.Excellent teamwork and communication skills
5.English/Spanish/French mother tongue, High level of spoken and written English a must

Preferred education/experience:
1.B.Sc./M.Sc. in Biotechnology/Chemistry/Biology
2.Minimum 2 years experience pharmaceutical product sales, working with customers abroad
3.Successful track record of generating revenue and business negotiations
4.Demonstrating to scientific/ non scientific audience.
5.Presentation ability

Willing to travel abroad 30-40% of the time.
Place of residence: North
 
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Pharmacist 

  Innodata Isogen Israel Ltd    Jerusalem Area, Work from home/Jerusalem   23/6/2010 
Category: Pharmacy/Pharmacology  
Education:   Position type: Full Time Employee  Experience:  
Area(s) of expertise desired: Pharmacology  
Description:
Israeli subsidiary of US-based outsourcing company seeks a mother-tongue English, U.S. trained Pharmacist to join our team for a full time salaried temporary position. The work involves doing QA and training of drug indexing work.  
Requirements:
Requirements:
U.S. training and experience as a clinical pharmacist
PharmD preferred
Work is exclusively in English
Available to travel for two weeks of training starting the beginning of July 2010; additional travel may be required
Available for a three-month assignment (possibility of becoming permanent)
Must be legally eligible to work in Israel

Location: Jerusalem / home
Most of the work is from home, although one-two days a week may be required in our Jerusalem office (near Malcha Mall / Train Station).

Send resume to: israeljobs@INNODATA-ISOGEN.COM, indicating Pharmacist in the subject line. Please include your salary expectations in your cover letter.

If you previously submitted a resume to the company there is no need to reapply. Only suitable applicants will be contacted.
 
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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:
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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:
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we ask a regulatory person with 1-2 years of experience of work in the field that can work with our regulatory consultant  
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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.
 
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Manager Protein Purification 

  Mengo    Tel Aviv Area   23/6/2009 
Category: Biotechnology, Chemistry, Life Sciences, Pharmacy/Pharmacology, manager  
Education: Doctorate   Position type: Full Time Manager  Experience: 3 years 
Area(s) of expertise desired: Academic, Biochemistry, Chemistry, Protein Chemistry, Proteomics, protein purification  
Description:
Job Description:
Lead, design, develop and optimize purification processes for recombinant proteins as human therapeutics. Lead and manage the development of in-process control methods, characterization studies that evaluate percent recovery, consistency, purity, and stability of selected protein candidates. Industrial experience with techniques including different chromatographic methods, HPLC, SDS-PAGE, western blot, and ELISA is essential.
 
Requirements:
Preferred Qualifications:
Applicants should have a Ph.D. degree in Biological Sciences or Chemistry and demonstrated experience in the Biotech industry with development of purification processes for recombinant proteins, preferably with managerial experience. Applicants must have profound theoretical knowledge of protein chemistry, be able to independently design integrated purification processes for a variety of proteins, supervise the operation of relevant equipment and have experience with a variety of chromatographic and separation techniques. Applicants must be task oriented, perform in a dynamic work environment where objectives can change and deadlines are critical. Excellent communication, teamwork and training skills are essential. Applicants must be fluent in English with strong ability to produce technical and scientific reports and documentation.

 
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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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Senior Researcher 

  L-IL - Top Talent Acquisition    Tel Aviv Area   27/2/2009 
Category: Chemistry, Life Sciences, Pharmacy/Pharmacology  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired:  
Description:
Managing products physiability checking alignment
Joint venturing with international companies
 
Requirements:
MSC in chemistry or pharmaceutics
Experience in transdermatic applications
Experience in large pharmaceutical companies an advantage
English native speaker
Knowledge and experience in negotiations management

 
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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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Analytical Chemist 

  Galpharma - pharmaceutical industries ltd.    Sharon Area, Or-Akiva   12/2/2008 
Category: Chemistry, Pharmacy/Pharmacology  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired: Analytical Chemistry, GMP, Laboratory, Quality Control  
Description:
Analytical laboratory
Galpharma - Pharmaceutical Industries ltd  
Requirements:
Knowledge and expiriene in the field of analytical chemistry and equipment  
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