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 183  View Titles Only  Page 1 of 19
 
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.  
To submit your resume , please sign in...
 
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.  
To submit your resume , please sign in...
 
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
 
To submit your resume , please sign in...
 
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.  
To submit your resume , please sign in...
 
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  
To submit your resume , please sign in...
 
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:
 
To submit your resume , please sign in...
 
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:
 
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...
 
management 

  Stiepleman Plc    Worldwide   31/5/2008 
Category: Biotechnology  
Education:   Position type: Full Time Employee  Experience:  
Area(s) of expertise desired:  
Description:
Well 1980  
Requirements:
management  
To submit your resume , please sign in...
 
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.

 
To submit your resume , please sign in...
 
View saved jobs  
 View Titles Only Page 1 of 19
 
 
מטפלת מאגר מטפלות לילדים , אופרייות לוח דרושים הגדול בישראל כולל אלפי הצעות עבודה
 

Copyright 2005-2019 Biotech Jobs in Israel