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Job Search Results: Jobs 1 - 10 of 179  View Titles Only  Page 1 of 18
 
Title   Company Name     Location   Date  
Postdoctoral/Research Associate in Cancer Biology at Ariel University 

  Ariel University    Yehuda & Shomron, Ariel   25/1/2016 
Category: Cancer biology research  
Education: Post-Masters   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Animal Services, Biology, Cell Culture, Genetics, Genomics, Laboratory, Molecular Biology, Research  
Description:
Working under general supervision of the principal investigator, the research assistant will plan and carry out studies focused on cancer cell biology. The research assistant will maintain critical cell lines, as well as work in animal models (mice). The overall goal of the laboratory is to understand the key factors that render melanoma aggressive and resistant to therapy, and to then develop better alternative therapies that can overcome the disease.The research work performed in the principal investigators laboratory is in line with the overall mission of the Institute for Personalized Medicine at Ariel University, in particular in enhancing human health by advancing discoveries from the laboratories to patients (translational research).  
Requirements:
ESSENTIAL FUNCTIONS:
1. Conduct experiments in both cell lines and mouse cancer models; record data and analyze results.
2. Assist in developing improved techniques, projection methods or procedures.
3. Maintain rodent colonies and perform experiments on melanoma mouse models.
4. Maintain careful and detailed laboratory notebooks.

QUALIFICATIONS: Education/Experience: PhD/MSc in biological sciences and a minimum of 2 year biological research experience. Previous experience working with animals preferred. Excellent oral and written communication skills and interpersonal skills.  
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Research Assistant in Cancer Biology at Ariel University 

  Ariel University    Yehuda & Shomron, Ariel   27/1/2016 
Category: Cancer biology research  
Education: Post-Bachelors, Pre-Masters   Position type: Full Time Employee  Experience: 1 year 
Area(s) of expertise desired: Animal Services, Biology, Cell Culture, Genetics, Genomics, Laboratory, Molecular Biology, Research, Toxicology  
Description:
Working under general supervision of the principal investigator, the research assistant will plan and carry out studies focused on cancer cell biology. The research assistant will maintain critical cell lines, as well as work in animal models (mice). The overall goal of the laboratory is to understand the key factors that render melanoma aggressive and resistant to therapy, and to then develop better alternative therapies that can overcome the disease.The research work performed in the principal investigators laboratory is in line with the overall mission of the Institute for Personalized Medicine at Ariel University, in particular in enhancing human health by advancing discoveries from the laboratories to patients (translational research).  
Requirements:
ESSENTIAL FUNCTIONS:
1. Conduct experiments in both cell lines and mouse cancer models; record data and analyze results.
2. Assist in developing improved techniques, projection methods or procedures.
3. Maintain rodent colonies and perform experiments on melanoma mouse models.
4. Maintain careful and detailed laboratory notebooks.

QUALIFICATIONS: Education/Experience: MSc/BSc in biological sciences. Previous experience working with animals preferred.  
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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%
 
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director 

  ERICPOSEY CO LTD    Worldwide, FLUSHING   7/1/2011 
Category: QA - Quality Control, Pharmacy/Pharmacology  
Education: Masters   Position type: Full Time  Experience: 1 year 
Area(s) of expertise desired: Academic, Finance  
Description:
Degree Evaluation Interviews Networking ... A less positive attribute of this job search method is that numerous ... However, the main reason why companies refrain from massively posting job details is that employers ... Community Internet Sites Many Israeli cities/regions have dedicated  
Requirements:
Degree Evaluation Interviews Networking ... A less positive attribute of this job search method is that numerous ... However, the main reason why companies refrain from massively posting job details is that employers ... Community Internet Sites Many Israeli cities/regions have dedicated  
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147861 Field Service Engineer - USA 

  CPS    Worldwide   25/3/2008 
Category: Biotechnology, Engineering, Life Sciences, Medical Equipment, IT/Hardware/Software  
Education:   Position type: Full Time Employee  Experience:  
Area(s) of expertise desired:  
Description:
this position is a "roving" position that should be based in new jersey.
the field service engineer [fse] is responsible for the implementation of the company systems at designated medical centers. this role is the primary liaison between the medical center and the company hq for technical and training issues.
primary responsibilities:
responsible for installation, maintenance, troubleshooting and repair of optic-mechanical equipment in the field of medial devices. provide product support, software and hardware, installation, operation & servicing training to customers.
provides weekly status reports, maintains up-to-date database and field service reports.
conducts classroom, on-site and online (remote) training with the customer.
modifies, develops and maintains end-user training materials/guides.
develops and administers customer competency exams - including scoring exams, communicating results, and suggesting remedial action where needed.
facilitates system enhancement requests, system corrections, and customer issues in relevant software.
qualifications:
technical professional with expertise in a healthcare regulated environment. bachelor degree in a technical discipline, with at least 4 years practical work experience in a technical healthcare environment and medical multidisciplinary (mechanics, optics, electronics, software, etc.) devices.
demonstrated success in working with customers (mainly hospitals), vendors, and leading cross-functional teams. interpersonal skills and customer service orientation.
strong process orientation, problem solving & troubleshooting skills, and a firm commitment to quality operating with various computer software.

excellent presentation, communication and conflict management skills.
knowledgeable in the system design, build, testing, training, supporting and go-live activities.
willingness to travel up to 80%, including overnight stays with trips to the company headquarters in israel.
displays professional, team-oriented attitude to co-workers and customers.
ethics and integrity - strong interpersonal with a high degree of self-motivation and ability to work independently away from the headquarters, peers and managers. responsible, independent and accurate.
excellent verbal communication skills.

a calm, helpful demeanor and the ability to handle deadlines and cope with stressful situations.  
Requirements:
 
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$105,000+ Year... Pharmacy Regional Manager Interview Now! 

  LMN and Associates    Worldwide, Sudbury   16/5/2010 
Category: Regulatory Affairs, Healthcare  
Education: Bachelors   Position type: Full Time Manager  Experience: 2 years 
Area(s) of expertise desired: Clinical Research, Genetics, Pharmacokinetics, Pharmacology  
Description:
Attention: $105K Pharmacy Regional Manager Needed!!

The primary purpose of this position is to manage RX Managers within a specific region.
This is a field position so some travel would be required.

The Compensation:
Base Salary - $105,000 - $120,000

Benefits:
Outstanding comprehensive benefit plan

For consideration you must act now!
Send resume today to
lnembhardassociates@gmail.com

LMN and Associates
Executive Recruitment
 
Requirements:
Experience / Requirements:
Must have prior regional or management experience.
Must be a licensed pharmacist in Ontario or be able to obtain licensing.
Must be able to travel.  
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head of oncology department 

  LR GROUP    Worldwide   29/8/2007 
Category: Healthcare  
Education:   Position type: Full Time Manager  Experience: 10+ years 
Area(s) of expertise desired: Oncology, radiotherapist  
Description:
 
Requirements:
 
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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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Senior Sales Executive 

  OB Recruitment Inc    Worldwide, New York   6/7/2007 
Category: Life Sciences  
Education: Bachelors   Position type: Full Time Employee  Experience: 8 years 
Area(s) of expertise desired: Start-Up  
Description:
Can be based from anywhere in the USA but prefer candidate to be on the East Coast.

Our Client is looking for a Senior Sales Executive to build a solid, predictable sales pipeline to meet sales targets. Given the complex, lengthy and consequently expensive, sales cycle it is critical to successfully manage the process of converting qualified prospects into fully licensed customers, while constantly striving to minimize the cost of sale. The successful candidate will report effectively and efficiently on the status of the sales pipeline to VP Sales & Marketing and the Chief Executive Officer.

The typical profile of the successful applicant would be a mature, confident and committed with a demonstrable track record of consistently exceeding targets. Furthermore, the successful candidate must have developed high levels of new business within the software sector, selling $1m deals at board level. The right candidate will be strongly self-motivated, an innovative and independent thinker who will bring an assertive style and individual approach to the new business sales model.

Experience in pharmaceuticals, biotechnology or electronics research sectors would be a considerable advantage. Candidates with direct sales and/or channel sales experience of complex high value software products are required.
Key Tasks
Achieving targeted annual sales of software, consultancy and training services.
Developing and implementing a strategic approach to sales in major direct accounts.
Report regularly and comprehensively to the executive team on all sales matters as required.
Manage the sales process from prospecting through to deal negotiation to satisfy sales objectives.
Ensure that strategic plans are completed and maintained for an agreed core list of clients and prospects.
Prospect identification within assigned territory.
Bid managing response to RFPs.
Co-ordination of appropriate resources as part of the sales process.
Negotiating (with management approval) client contracts and licenses.
Account managing client during project implementation (ensuring client satisfaction) and ensuring client payment.
Achieving follow on/up selling into account base of new products and services.
Working with colleagues in other territories to achieve global sales.
Determining price and volume discount policies in conjunction with executive staff.
Providing a substantial input to forecasting and setting sales quotas for the channel network.

Key Relationships
Reporting relationship reporting to VP Sales & Marketing & CEO.
Establish and maintain close working relationships with opposite numbers and other relevant personnel with Client's partners with a view to optimizing sales and overall corporate success.

 
Requirements:
Key Expectations
Expected to travel extensively.
Flexibility in a new and developing organization.
Experience in implementing enterprise-wide IT systems would be seen as an important advantage  
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Clinical Research Scientist 

  Makro Technologies    Worldwide   28/11/2006 
Category: QA - Quality Control, Biotechnology, Engineering, Chemistry, Regulatory Affairs  
Education: Bachelors   Position type: Full Time Executive  Experience: 4 years 
Area(s) of expertise desired: Clinical Data Management, Clinical Research, Regulatory Affairs, Research  
Description:
Full Requirement : Complete Description: Drafts protocols, formulates requirements for clinical supplies and develops CRFs.As a Clinical Research Scientist, you will participate in preparation of routine clinical documents (i.e. protocols, CRFs, GMRs, ICFs, etc.). You will prepare complex documents with moderate supervision and routine documents independently as directed by supervisor ( AHT, CAP, CDP, IND documents, etc.). You will evaluate and select potential investigative sites with minimal to moderate supervision. You will organize and present complex aspects of protocol design at investigator and internal meetings. You will also conduct initiation/monitoring visits independently, coordinate and monitor activities at clinical/investigational sites with minimal supervision by medical monitors and/or project monitors. You may also participate in training/mentoring new hires. You will oversee and coordinate the collection of and/or collect pre-study documents independently. You will monitor safety with minimal to moderate supervision via any of the following: telephone contacts, study event reports, case report form/safety report reviews, contacts with regional clinical associates (RCA), RCA monitoring trip reports, or direct site visits. You will also participate in data review and discrepancy resolution, team meetings/presentations with increasing levels of independence and may serve as Study Team Leader as well as a member of a broad range of CR&D-related and ad hoc committees as needed. You may represent organizational unit at research-wide meetings and on committees, including Global Clinical Project Teams and Interdepartmental Project Teams. In addition, you will serve as a clinical science resource for the team(s), and for peers and/or subordinates.  
Requirements:
Qualification & Skills:A BS or equivalent with a minimum of 5 years related experience or a MS degree or equivalent in Life Sciences with a minimum of 4 years related experience is required. You must have good interpersonal skills. You must have the ability to work with and negotiate with colleagues to find solutions to resource/supplies/timeline issues.  
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