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Job Search Results: Jobs 1 - 9 of 9  View Titles Only  Page 1 of 1
 
Title   Company Name     Location   Date  
Director/VP Sales and Marketing 

  Mengo    North Area, Cessaria   17/10/2010 
Category: Sales/Marketing  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired: Marketing  
Description:


Provide leadership and coordination of company sales and marketing functions. Develop and implement sales and marketing strategy. Monitor and analyze sales and marketing activity against goals.






 
Requirements:
PRIMARY RESPONSIBILITIES
Direct and coordinate company sales and marketing functions.
Develop and coordinate sales selling cycle and methodology.
Responsible for revenue forecast and revenue generation in the company
Direct and oversee the company marketing function to identify and develop new customers/reps./distributors for the company's products
Develop strategies and plans which identify marketing opportunities, direct marketing, and new project development.
Analyze and evaluate the effectiveness of sales, methods, costs, and results.
Develop and manage sales and marketing budgets
Directly manage major and critical developing client accounts, and coordinate the management of all other accounts.
Participate in the development of new project proposals.
Establish and implement short- and long-range goals, objectives, policies, and operating procedures.
Supervise the planning and development of company marketing and communications materials.
Develop and supervise the preparation, issuance, and delivery of sales materials, exhibits, and promotion programs.
Promote positive relations with partners, vendors, and distributors.
Recommend and administer policies and procedures to enhance operations.
 
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Director/VP Sales and Marketing 

  Mengo    North Area, Cessaria   17/10/2010 
Category: Sales/Marketing  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired: Marketing  
Description:


Provide leadership and coordination of company sales and marketing functions. Develop and implement sales and marketing strategy. Monitor and analyze sales and marketing activity against goals.






 
Requirements:
PRIMARY RESPONSIBILITIES
Direct and coordinate company sales and marketing functions.
Develop and coordinate sales selling cycle and methodology.
Responsible for revenue forecast and revenue generation in the company
Direct and oversee the company marketing function to identify and develop new customers/reps./distributors for the company's products
Develop strategies and plans which identify marketing opportunities, direct marketing, and new project development.
Analyze and evaluate the effectiveness of sales, methods, costs, and results.
Develop and manage sales and marketing budgets
Directly manage major and critical developing client accounts, and coordinate the management of all other accounts.
Participate in the development of new project proposals.
Establish and implement short- and long-range goals, objectives, policies, and operating procedures.
Supervise the planning and development of company marketing and communications materials.
Develop and supervise the preparation, issuance, and delivery of sales materials, exhibits, and promotion programs.
Promote positive relations with partners, vendors, and distributors.
Recommend and administer policies and procedures to enhance operations.
 
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Assistant VP RA/QA 

  Mengo    North Area, Cessaria   17/10/2010 
Category: Clinical Research, Regulatory Affairs  
Education:   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Clinical Data Management, Clinical Research, Quality Assurance, Regulatory Affairs  
Description:

i. Assist VP RA/QA in the following:
1. Manage the informed consent document
2. Manage safety reporting
3. Assist in the preparation of documentation for the study approval and running phases (submissions, responses to regulatory authorities, investigator brochure, progress/annual reports, amendments etc)
4. Maintain Company's Document Control center  
Requirements:
Assist Clinical Quality Manager in the following:
1. Assist Clinical Trial Managers in maintaining in-house study binders
2. Review monitoring reports
3. Assist in follow up of post audit CAPA
4. Review protocol deviations
iii. Israel CRA
1. Perform monitoring trial activities in the local Israeli sites
2. Experience/Skills Required
a. 2-3 years minimum work experience as a CRA
b. High level of English writing skills
c. Experience preparing informed consents and other clinical study related documentation (investigator brochure, progress/annual reports etc)
d. Excellent communication, organizational and recordkeeping skills required
e. Must be able to work in a fast-paced environment with demonstrated ability to juggle multiple competing tasks and demands

3. Required Education
a. Formal CRA training (e.g. BioForum CRA course or in-house CRO courses)
b. Bachelors degree in life science-related field
c. Related degree with an equivalent combination of education and experience will be con
 
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Applications Development Engineer (position # 1213) o 

  Mengo    North Area, Yokneam   14/5/2010 
Category: Clinical Research  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired:  
Description:

Please send your resume in a .doc format to jobs2@mengo.co.il
You must indicate at the headline of your email the no. of the position 1213


Duties & Responsibilities:
Responsible for all operational aspects of pre and clinical trials including all related logistics, communication and coordination with the operating room staff.
Budget, follow up and control of project plans
Managing the technology and clinical databases at DHF standards.
Take active part in integrating technological solutions into the product/application being developed.
Managing tasks with external organizations and staff (e.g. hospitals, labs, suppliers).
Testing of prototypes for clinical performance and engineering evaluation.
Responsible for managing all stages of pre and clinical trials from design to final report including procedural monitoring and documentation (protocols, instruments and accessories order, sterilization etc).
Follow PDI processes related to product definition to release.
 
Requirements:
Academic B.Sc. or preferred M.Sc in either: bio-medical engineering, medical science, medicine (MD) or similar.
At least 3 year experience in a medical device company.
Ability to design and support clinical trials as well as to execute technical tests (protocols, implementation, reports).
Good technical capabilities and creativity.
Familiarity with operating rooms environment and equipment and with surgical procedures - advantage.

Personal
English fluent talking and high level writing - mandatory.
Quick learning curve.
High diligence.
Assertive.
High pressure and workload capabilities.
Teamwork oriented.
 
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Clinical Application Development Scientist (position # 1296) o 

  Mengo    North Area, Yokneam   14/5/2010 
Category: Clinical Research, Medical Equipment  
Education:   Position type: Full Time  Experience: 4 years 
Area(s) of expertise desired: Clinical Research, Surgery  
Description:
Please send your resume in a .doc format to jobs2@mengo.co.il
You must indicate at the headline of your email the no. of the position 1296

Affiliation: reporting to the Medical Director

Job Description and Main Tasks:
Acquisition, analysis and reporting of application related technological, scientific and clinical data including and maintenance of a clinical and scientific database (scientific literature, internet, market reports, etc.).
Professional support of the Medical Director activities including: writing protocols, multi-centers studies, coordination with physicians, laboratories and hospitals, issuing reports, etc.
Writing reports for in-house and external purposes and preparing multimedia presentations.
Assisting in writing scientific papers.
Working closely with bodies within and outside the company including CROs, clinical monitors, MDs nurses, etc.
Active participation in the R&D Application Group activities.
 
Requirements:

Qualifications:
Academic M.Sc. or preferred Ph.D. in either: bio-medical engineering, medical science, biology, medicine (MD) or equivalent.
At least 5 year experience in a medical device company.
Mother tongue level English.
Ability to read and analyze high volumes of scientific data.
Journal level scientific papers writing capability.
Familiarity with operating rooms environment and equipment and with surgical procedures.
Familiarity with regulatory processes (FDA, CE, IRB) - advantage.
Reliability, team worker, excellent inter-personal relationships.


 
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CEO is needed for a pharmaceutical company 

  Mengo    Jerusalem Area, jerusalem   23/9/2009 
Category: Biotechnology, Clinical Research, Management/Executive, Pharmacy/Pharmacology, "  
Education: MBA   Position type: Full Time Executive  Experience:  
Area(s) of expertise desired: Executive, Oncology, "/CEO  
Description:
Experience with accompanying Clinical Trials in the field drugs , preferably oncology drugs .


Experience in Business Development.


Experience from a startup company and preferably from a public company.


Experience with raising capital - as advantage.


The role includes travelling abroad.
 
Requirements:
Experience with accompanying Clinical Trials in the field drugs , preferably oncology drugs .


Experience in Business Development.


Experience from a startup company and preferably from a public company.


Experience with raising capital - as advantage.


The role includes travelling abroad.
 
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software engineer C++ 

  Mengo    Tel Aviv Area   16/7/2009 
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, , software  
Description:
 
Requirements:
 
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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.

 
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VP/ Director RA / QA 

  Mengo    All   8/5/2009 
Category: QA - Quality Control, Biotechnology, Pharmacy/Pharmacology, Medical Equipment, Regulatory Affairs  
Education:   Position type: Full Time Executive  Experience:  
Area(s) of expertise desired: Medical Device, Pharmacology, Quality Assurance, Regulatory Affairs  
Description:
Responsibilities:

1. To establish, maintain and improve the quality system in accordance with 21CFR820, ISO9001 and ISO13485
2. To act as the management representative as defined in the quality system responsible for:
ensuring that quality system requirements are effectively established and maintained; and
reporting the performance of the quality system to senior management for review

3. To manage the following quality system processes to ensure compliance with the applicable regulations, standards and directives including:
Documentation control, auditing, training, management review, complaints, product quality acceptance, supplier control, change control and quality planning.

4. Assist with the preparation, filing, and negotiation of submissions to regulatory bodies to obtain market or clinical research approvals including ongoing trials and post-approval activities.
5. Review clinical trial documents including clinical protocols/reports, investigator brochures, nonclinical reports, CMC protocols/test methods;
6. Reviews labeling, promotional material, product changes and documentation for changes requiring government approval
7. Monitor changes to domestic and international regulations and standards and ensure compliance with those regulations and standards
 
Requirements:
Qualifications:

** More than 10 years experience in the Biopharmaceutical or Medical Device industries.
**At least 5 years management experience in Quality assurance and Regulation in Biopharmaceutical or Medical Device industries.
** Experience with Notified Bodies in Europe.
** Experience with quality requirements for clean rooms and sterilization

 
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