|
|
|
Work as a software developer without experience - for graduate students |
|
|
|
Category: |
Biotechnology, Engineering, Chemistry, Life Sciences, Pharmacy/Pharmacology, Healthcare, IT/Hardware/Software
|
|
|
Education: |
Bachelors |
Position type: |
Full Time |
Experience: |
No experiece |
|
|
Area(s) of expertise desired: |
|
|
|
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.
|
|
|
Requirements: |
Bachelor's degree average of 85 and above.
Independent learning ability.
high-level English.
|
|
|
|
|
| |
|
|
Project Manager |
|
|
|
Category: |
Biotechnology, IT/Hardware/Software
|
|
|
Education: |
Bachelors |
Position type: |
Full Time Employee |
Experience: |
2 years |
|
|
Area(s) of expertise desired: |
Medical Tech, Project Management, Software Development
|
|
|
Description: |
● Monitor and create project management and general governance
processes
● Work with consultants to meet regulatory requirements, incl
designing and applying processes as well as documentation to
demonstrate compliance
● Ensure team tasks are assigned and completed
● Ensure planning for required resources
● Optimise reporting
● Optimise task tracking
● Keep team camaraderie and morale high (incl utilising support
staff to engender best possible environment)
● Help ‘onboard’ new staff
● Produce Weekly Release contents and plans such as Kanban
boards, Gantt charts, etc
● Include Estimates and Time Tracking so we can better estimate
and plan client delivery dates
● Work with external quality consultants to ensure processes are
working efficiently and continuously improved
|
|
|
Requirements: |
● 2+ years in project management, following an SDLC
● Strong analytical and organisational skills
● Clear communicator and builder of relationships regardless of job
role/culture
● Microsoft Word, Excel and PowerPoint
● Fluent English, spoken Hebrew
● Advantage: Familiarity with extending project management tools
especially YouTrack Workflows (equivalent tools such as Jira also
a plus)
● Advantage: Working with ISO and other standards for
development
● Advantage: medical software experience
|
|
|
|
|
| |
|
|
Computerized systems validation engineer |
|
|
|
Category: |
QA - Quality Control, IT/Hardware/Software
|
|
|
Education: |
Bachelors |
Position type: |
Full Time |
Experience: |
No experiece |
|
|
Area(s) of expertise desired: |
Business Analyst, Compliance, GLP, GMP, Information Systems, Medical Device, Other, Professional Services, Validation
|
|
|
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.
|
|
|
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
|
|
|
|
|
| |
|
|
manager |
|
|
|
Category: |
QA - Quality Control, IT/Hardware/Software
|
|
|
Education: |
Masters |
Position type: |
Full Time Manager |
Experience: |
6 years |
|
|
Area(s) of expertise desired: |
Academic
|
|
|
Description: |
|
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.
|
|
|
Requirements: |
|
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.
|
|
|
|
|
| |
|
|
software engineer C++ |
|
|
|
Category: |
Engineering, Medical Equipment, IT/Hardware/Software
|
|
|
Education: |
Bachelors |
Position type: |
Full Time Employee |
Experience: |
5 years |
|
|
Area(s) of expertise desired: |
Academic, Other, Software Development, úåëðä , software
|
|
|
Description: |
|
|
|
Requirements: |
|
|
|
|
|
| |
|
|
Software / Image processing engineer |
|
|
|
Category: |
Medical Equipment, IT/Hardware/Software
|
|
|
Education: |
Bachelors |
Position type: |
Full Time |
Experience: |
3 years |
|
|
Area(s) of expertise desired: |
Software Development, Image processing
|
|
|
Description: |
Medical Imaging product development experience in image processing.
Design and develop concepts for new algorithms. Design and implemention of GUI. Debugging and system integration. Interact with customers
|
|
|
Requirements: |
3+ years experienced with C/C++.
Strong understanding of Object Oriented Design (OOD) and Programming (OOP).
Extensive knowledge experience in one of the following: Image Processing/Image recognition processing - preferred.
Oral and written communication skills in English – Must.
Strong problem solving and troubleshooting skills.
Ability to work in a team, ability to work independently.
Commitment to work plans and schedules.
Creativity, Self learner, Quick learner.
Education
Masters/Bachelor degree in engineering (Computer, Electronics).
|
|
|
|
|
| |
|
|
Sales |
|
|
|
Category: |
IT/Hardware/Software
|
|
|
Education: |
Bachelors |
Position type: |
Full Time Employee |
Experience: |
2 years |
|
|
Area(s) of expertise desired: |
General Services
|
|
|
Description: |
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
|
|
|
Requirements: |
Bachelor of Science – Nursing or equivalent
Proven organizational, observational, interpersonal and communication skills
|
|
|
|
|
| |
|
|
CRA |
|
|
|
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 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.
|
|
|
Requirements: |
MD
Fluent official language of the country
English, written and spoken, upper intermediate
PC user
|
|
|
|
|
| |
|
|
Medical Advisor-Greece |
|
|
|
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.
|
|
|
|
|
| |
|
|
R & D MANAGER |
|
|
|
Category: |
Engineering, Medical Equipment, IT/Hardware/Software
|
|
|
Education: |
|
Position type: |
Full Time Executive |
Experience: |
5 years |
|
|
Area(s) of expertise desired: |
|
|
|
Description: |
|
|
|
Requirements: |
Bsc in Electrical Engineering
· Few years of experience in board design
· Few years of experience in managing small projects with many point
· of contacts
· Few years of experience in working with micro-controllers, specifically ARM processors
· Experience in working with sub-contractors, 3rd party companies and external consultants.
· Good understanding of algorithmic design and digital design flows
· Understanding of software methodologies
· Ability to define requirements and derive specifications
· Experience with real-time design - an advantage
· Experience with bio-signal processing - an advantage
|
|
|
|
|
| |
|
