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Work as a software developer without experience - for graduate students |
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Category: |
Biotechnology, Engineering, Chemistry, Life Sciences, Pharmacy/Pharmacology, Healthcare, IT/Hardware/Software
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Education: |
Bachelors |
Position type: |
Full Time |
Experience: |
No experiece |
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Area(s) of expertise desired: |
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Description: |
InfinityLabs R&D(a Matrix company) is looking for Graduates with high grades who want to develop a career! You have the option to change your future by 180 degrees. If you have high analytical capabilities and you are interested to work in the high-tech industry - this is your chance to try your luck and test your suitability for work as a software developer. Qualifying will be given training at the expense of the company.
Full-time job.
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Requirements: |
Bachelor's degree average of 85 and above.
Independent learning ability.
high-level English.
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Extra Money in a new Sales Project |
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Category: |
Biotechnology, Chemistry, Life Sciences, Pharmacy/Pharmacology, Healthcare, Sales/Marketing
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Education: |
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Position type: |
Full Time Employee |
Experience: |
No experiece |
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Area(s) of expertise desired: |
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Description: |
International nutrition company is looking for 5 new employees to join a dynamic sales team.
Challenging job in marketing & sales.
Min 10 hrs/week.
Extra 2000-4000 nis (predictable income)
Option to work from home.
Please send CV to: project@slimail.com
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Requirements: |
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Please send CV to: project@slimail.com
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Medical Director |
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Category: |
Management/Executive, Medical Management, Medical Equipment, Healthcare
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Education: |
Doctorate |
Position type: |
Full Time |
Experience: |
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Area(s) of expertise desired: |
Clinical Research, Medical Affairs, Medical Device, Ophthalmology, Regulatory Affairs, Research, Start-Up, Surgery
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Description: |
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Requirements: |
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Clinical Research Physician |
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Category: |
Clinical Research, Management/Executive, Medical Management, Healthcare
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Education: |
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Position type: |
Full Time Manager |
Experience: |
No experiece |
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Area(s) of expertise desired: |
Academic, Internal Medicine, Oncology
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Description: |
A leading international pharmaceutical company is seeking a Medical Doctor specializing in Oncology for the position of Clinical Research Physician. The CRP will manage medical domains, be responsible for the clinical studies, serve as professional authority supporting Marketing, and develop relations with opinion leaders.
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Requirements: |
An intern with sub-specialty in Oncology and experience in the Pharmaceutical Industry.
A medical graduate / Oncology specialist, experienced in the Pharmaceutical Industry will be considered too.
English – fluent.
Analytic skills, presentation & communication skills.
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Director, Manufacturing |
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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
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Education: |
Bachelors |
Position type: |
Full Time Manager |
Experience: |
10+ years |
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Area(s) of expertise desired: |
Bioanalytical Services, Biology, Manufacturing/Production
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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.
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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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Junior Sales Representative Surgical |
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Category: |
QA - Quality Control, Biotechnology, Engineering, Chemistry, Clinical Research, Clerical/Administrative, Management/Executive, Medical Management, Pharmacy/Pharmacology, Medical Equipment, Regulatory Affairs, Healthcare, Sales/Marketing
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Education: |
Bachelors |
Position type: |
Full Time |
Experience: |
3 years |
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Area(s) of expertise desired: |
Medical Affairs, Medical Device, Sales
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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. We’re 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
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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, you’ll 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
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$105,000+ Year... Pharmacy Regional Manager “Interview Now!” |
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Category: |
Regulatory Affairs, Healthcare
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Education: |
Bachelors |
Position type: |
Full Time Manager |
Experience: |
2 years |
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Area(s) of expertise desired: |
Clinical Research, Genetics, Pharmacokinetics, Pharmacology
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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
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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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Medical Director |
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Education: |
Doctorate |
Position type: |
Part Time |
Experience: |
4 years |
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Area(s) of expertise desired: |
Formulation, Internal Medicine, Medical Tech, Pharmacology, Professional Services, Start-Up
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Description: |
A Biotech Start-up company
Is seeking
A Medical Director
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Requirements: |
- Israeli license to practice medicine
- Internal doctor – a plus
- At least 4 years of experience in drug development
- Part time job in Jerusalem
- Mother-tongue level English
For additional jobs please visit www.hever.co.il
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nurses |
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Education: |
Associate |
Position type: |
Full Time Employee |
Experience: |
No experiece |
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Area(s) of expertise desired: |
Nursing
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Description: |
job in Retiremennt and Caregiving Centres
• Responsible for assessing, planning, implementing and evaluating physical, psychological, emotional, spiritual, cultural and social needs of the resident
• Validates the plan of care, goals and objectives with the resident/family
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Requirements: |
• Bachelor of Science – Nursing or equivalent
• Proven organizational, observational, interpersonal and communication skills
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CRA |
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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
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Education: |
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Position type: |
Full Time |
Experience: |
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Area(s) of expertise desired: |
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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 company’s 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.
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Requirements: |
MD
Fluent official language of the country
English, written and spoken, upper intermediate
PC user
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