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Healthtech & life science positions across aMoon Fund Portfolio |
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Category: |
QA - Quality Control, Chemistry
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Education: |
Doctorate |
Position type: |
Full Time Employee |
Experience: |
2 years |
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Area(s) of expertise desired: |
Academic, Administration, Analytical Chemistry, Applied Chemistry, Biochemistry, Bioinformatics, Biology, Business Analyst, Business Development, Chemistry, Clinical Data Management, Clinical Research, Executive, Finance, GLP, GMP, Human Resources, Manufacturing/Production, Medical Affairs, Medical Device, Molecular Biology, Neurosciences, Nutrition, Orthopedics, Pharmacokinetics, Pharmacology, Postdoctoral, Process Development, Production Planning, Professional Services, Project Management, Purchasing, Quality Control, Radiology, Regulatory Affairs, Research, Start-Up, Technical Services
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Description: |
aMoon is a leading Israeli venture capital. We invest in companies that are accelerating cures for the world’s most life-threatening conditions and providing solutions for global healthcare’s biggest cost drivers. Our mission is to identify, invest, and drive growth in companies of all development stages across biopharmaceutical, device, and digital technologies.
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Requirements: |
With over 30 local vacancies in leading healthtech & life sciences companies we encourage you to visit our job board!
https://jobs.amoon.fund/
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Healthtech & life science positions across aMoon Fund Portfolio |
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Category: |
QA - Quality Control, Chemistry
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Education: |
Doctorate |
Position type: |
Full Time |
Experience: |
2 years |
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Area(s) of expertise desired: |
Academic, Biochemistry, Biology, Business Analyst, Business Development, Cell Biology, Clinical Data Management, Clinical Research, Communications, Genetics, GMP, Human Resources, Immunology, Infectious Disease, Internal Medicine, Manufacturing/Production, Marketing, Medical Device, Neurosciences, Pharmacology, Postdoctoral, Process Development, Production Planning, Professional Services, Project Management, Quality Assurance, Quality Control, Regulatory Affairs, Research, Sales, Software Development, Start-Up
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Description: |
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aMoon is a leading Israeli venture capital. We invest in companies that are accelerating cures for the world’s most life-threatening conditions and providing solutions for global healthcare’s biggest cost drivers. Our mission is to identify, invest, and drive growth in companies of all development stages across biopharmaceutical, device, and digital technologies.
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Requirements: |
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With over 30 local vacancies in leading healthtech & life sciences companies we encourage you to visit our job board!
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Clinical and Quality Assurance Manager |
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Category: |
QA - Quality Control, Clinical Research
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Education: |
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Position type: |
Full Time |
Experience: |
5 years |
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Area(s) of expertise desired: |
Clinical Research, Medical Device, Orthopedics, Quality Assurance, Start-Up
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Description: |
Manages all clinical aspects of a clinical study, including:
•Assesses operational feasibility and recommends study execution plan; participates in site monitoring visits as appropriate.
Select countries and sites for trial participation; develops relationships with K.O.L and site staff; coordinates and assists in the planning of regulatory or ethics committee activities, as appropriate;
•Design clinical trial protocols;
•Prepares/reviews site study documents
•Manages clinical monitoring activities (including approval of visit report templates, monitoring plan, etc.)
•Ensures all clinical trials are executed in compliance with ICH/GCP guidelines/regulations and applicable SOPs:
Manages all aspects of quality assurance activities including:
•Ensure compliance with FDA and other regulatory affairs
•Develop, administer and maintain quality assurance procedures and activities required to ensure that the company’s processes and products are in compliance with applicable quality standards and requirements
•Establish quality assurance and quality control inspection and testing procedures
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Requirements: |
•Minimum 5 years clinical trial management experience in a medical device company - Mandatory
•Advanced knowledge of Good Clinical Practices and current knowledge of FDA regulations for clinical trials is required;
•International clinical trial experience
•Minimum 2 years Quality Assurance experience in a medical device company - Mandatory
•Thorough knowledge of FDA Quality System requirements, ISO 13485:2003 (Quality System) requirements
•Knowledge of Good Manufacturing Practices (GMP) and applicable Quality System Standards
•Experience working with subcontractors
•Excellent English - written and verbal
•Excellent communication and organizational skills, along with problem solving,
Travel- Travel abroad required per week, per month
Location: Misgav Industrial Park
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experienced QA/RA professional |
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Category: |
QA - Quality Control, Biotechnology, Life Sciences, Medical Equipment, Regulatory Affairs, òáøéú åàðâìéú áøîä âáåää îàåã (÷øéàä, ëúéáä åãéáåø)
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Education: |
Masters |
Position type: |
Full Time |
Experience: |
3 years |
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Area(s) of expertise desired: |
GMP, Quality Assurance, Radiology, Regulatory Affairs
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Description: |
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We work with clients in the Medical Device field to build and implement their quality management system, as well as prepare regulatory strategy plans and files.
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Requirements: |
B.A. in Mechanical Engineering/ Quality Engineering/ Biotechnology/ Life Sciences
2 years of experience with medical device Quality and Regulatory requirements (ISO13485, GMP)
Experience in writing and submitting regulatory documents for the European and American regulatory bodies
Experience with CE regulatory requirements
Has participated at least once in a CE quality/regulatory audit
Languages: proficient in Hebrew and English (reading, writing and speaking)
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Computerized systems validation engineer |
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Category: |
QA - Quality Control, 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: |
Business Analyst, Compliance, GLP, GMP, Information Systems, Medical Device, Other, Professional Services, Validation
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Description: |
•Write Computerized systems validation documents and test protocols: STP,STD,IQ,OQ,PQ
•Write Computerized systems design and summary documents: URS,FRS,VP,STR,VSR
•Write SOPs ( Standard Operating Procedures) , Work instructions
•Write software applications reject lists, bug identification, report and monitoring.
•Functional testing of life-science computerized systems.
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Requirements: |
Minimum Qualifications
•Education: BA/BSC in Biotechnology, Chemical Engineering, Biomedical engineering, Chemistry, Biology, Computer Science
•Communication: Excellent oral and exceptional technical writing skills with the ability to interface effectively and professionally at all levels.
•Organized person with high ability to work with fine details.
•Excellent English( Equal to mother tongue).
•QA oriented : Experience with QA in the life-science industry( Pharma ,Biotech and Medical devices). Optional- Experience with QC in the life science industry.
•Service oriented.
Preferred Qualifications
•Experience with use of life science computerized system ( e.g. LIMS, ERP systems, computerized Lab systems ( Empower, FTIR etc..), production systems etc.)
•Experience with IT subjects (i.e. Server- Client topology, Data backups, Help Desk etc.)
•Experience in software testing\ computerized system validation in the life science industry
•Knowledge in roles and guidelines: 21CFRPart11, GAMP5 ISO 14971:2007,IEC 62304
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Account Executive Scientist |
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Category: |
QA - Quality Control
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Education: |
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Position type: |
Full Time Executive |
Experience: |
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Area(s) of expertise desired: |
Medical Device
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Description: |
We are looking for an Account Executive Scientist to devolop the Israeli market for an Internaitonal company.
Actively involved, through direct participation in office or field clients visits to understand client’s needs, provide technical scientific or regulatory solutions, provide regulatory or business presentations
Makes client visits, with a special emphasis on scientific and regulatory aspects to generate new sales, expand volume of testing, consulting or clinical from current and new clients and obtain marketing and competitive information.
Contribute to establish and Implement annual sales plans and assists in the development and achievement of sales goals through effective interaction with clients, Company Project Development Advisor (PDA), scientists, sales, agents and other technical staff worldwide.
Assists with major accounts management and development in Israel.
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Requirements: |
Scientific Degree: Veterinarian, Pharmacist, PhD, MD, Engineering
0-5 years experience related to the Medical Devices Industry, Manufacturing, Regulations or Testing
Biomaterials Science, Medical Devices evaluation principles and standards, Medical Devices regulations.
Substantial, professional communications skills and analytical capabilities.
Outstanding motivation skills required. Willingness to travel both in Israel and internationally. Hebrew & English language proficiency.
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manager |
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Category: |
QA - Quality Control, IT/Hardware/Software
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Education: |
Masters |
Position type: |
Full Time Manager |
Experience: |
6 years |
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Area(s) of expertise desired: |
Academic
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Description: |
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A management consulting firm, we are focused exclusively on the metals industry. Our objectives are to identify opportunities for clients to reduce the cost of new metal, improve the value received for scrap, manage price risk exposure and strengthen administrative and financial controls.
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Requirements: |
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A management consulting firm, we are focused exclusively on the metals industry. Our objectives are to identify opportunities for clients to reduce the cost of new metal, improve the value received for scrap, manage price risk exposure and strengthen administrative and financial controls.
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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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director |
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Category: |
QA - Quality Control, Pharmacy/Pharmacology
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Education: |
Masters |
Position type: |
Full Time |
Experience: |
1 year |
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Area(s) of expertise desired: |
Academic, Finance
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Description: |
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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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Requirements: |
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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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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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