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 11 - 20 of 30  View Titles Only  Page 2 of 3
 
Title   Company Name     Location   Date  
Chemist / A Research Management 

  halufa    North Area   7/3/2011 
Category: Chemistry  
Education: Doctorate   Position type: Full Time Team Leader  Experience: 10 years 
Area(s) of expertise desired: Analytical Chemistry, Chemical Engineering, Chemistry  
Description:
Require a leading industrial plant chemist / research manager
Education: Dr. in analytical chemistry
Masters degree in analytical chemistry with relevant experience of at least 10 years - a possible
Previous experience of between 8-10 years or more in research, analytical chemistry  
Requirements:
Proven administrative ability - Manage direct subordinates 3
Communication with external bodies
Previous experience in the field of phosphates - a significant advantage
Excellent human relations
Willingness to work hard  
To submit your resume , please sign in...
 
Engineering site manager 

  ETHOSIA    Jerusalem Area   20/1/2011 
Category: Engineering, Chemistry  
Education: Bachelors   Position type: Full Time  Experience: 8 years 
Area(s) of expertise desired: Engineering  
Description:
Leading engineering aspects at plant.
Leading engineering team.
Support all operational departments
Support projects progress.
Lead Eng projects.
Further optimization and development, malfunction reduction.
Specific support on HVAC, Machines and Control issues.  
Requirements:
Senior Mechanical engineer.
Min 8 yrs experience in Machines and controlled plants.
Proven ability to manage complex engineering activities.
Previous experience in managing of outsource vendors and work with international teams and suppliers.
Experienced with aseptic processes, automatic operations, controlled systems.
Familiar with pharmaceutical GMP
Deep technological understanding, problems solving abilities.
Team player, motivated, highly responsible and target oriented.  
To submit your resume , please sign in...
 
Junior Sales Representative Surgical 

  Covidien    Tel Aviv Area, Tel Aviv   27/12/2010 
Category: QA - Quality Control, Biotechnology, Engineering, Chemistry, Clinical Research, Clerical/Administrative, Management/Executive, Medical Management, Pharmacy/Pharmacology, Medical Equipment, Regulatory Affairs, Healthcare, Sales/Marketing  
Education: Bachelors   Position type: Full Time  Experience: 3 years 
Area(s) of expertise desired: Medical Affairs, Medical Device, Sales  
Description:


Position: Junior Sales Representative Surgical (3)
Location: Central Israel (Tel Aviv)

Covidien

It's a new era with nothing but promise. Today, Covidien is more than a leading provider of medical devices, supplies and pharmaceuticals. Were a $10 billion company with over 40,000 employees who are passionate about helping doctors, nurses, and other medical industry professionals to as effective they can be.
A company with a true global mindset, Covidien has forged dynamic partnerships with medical professionals around the world. In our role as an integral collaborator, we help identify patient needs and translate them into proven procedures and products that improve and save lives.

As a Junior Sales Representative Surgical focused on our prestigious products, you will work closely with doctors, surgeons and specialist groups, selling into hospitals and a variety of practices across the centre of Israel and Central region - Jerusalem.
In return, we will provide you with world-class training, frequent development opportunities, rewarding benefits and the opportunity to work in a varied, challenging role with a large scope for demonstrating your independence, innovation and your talent for sales.

As a Junior Sales Representative your main responsibilities will involve:

Selling a portfolio of world renewed Surgical products across your established customer base
Increasing sales in line with agreed budgets
Building on well established relationships, to become an expert advisor to healthcare professionals
Being resilient, a strong negotiator and advocate for your products whilst identifying new opportunities in your market place
Cooperating with Customer Service Department
Participating in preparation and monitoring outcome of tender offers within the territory

 
Requirements:
As a Junior Sales Representative your skills and qualifications will ideally include:

Comprehensive selling experience B2B business (preferably in medical environment)
Previous sales experience or the desire to develop your sales ability
Good command of English to business standard
A full clean Driving License

What we will be looking for in you:

This role will suit a performance-driven young individual who enjoys working in a competitive environment and seizes the opportunity to get the awards that over-achievement brings. Ideally, youll have excellent presentation and negotiation skills and genuinely enjoy building long-term, trusting relationships with your customers.

Contact:

To apply follow the link:
http://www.tycohealthcarecareers.com/tycohcinternational/jobboard/NewCandidateExt.aspx?__JobID 9449

 
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...
 
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.

 
To submit your resume , please sign in...
 
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

 
To submit your resume , please sign in...
 
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
 
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...
 
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  
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...
 
View saved jobs  
 View Titles Only Page 2 of 3
 
 
מטפלת מאגר מטפלות לילדים , אופרייות לוח דרושים הגדול בישראל כולל אלפי הצעות עבודה
 

Copyright 2005-2019 Biotech Jobs in Israel