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Job Search Results: Jobs 1 - 10 of 28  View Titles Only  Page 1 of 3
 
Title   Company Name     Location   Date  
Director, Manufacturing 

  Scientific Search    Worldwide   14/3/2011 
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  
Education: Bachelors   Position type: Full Time Manager  Experience: 10+ years 
Area(s) of expertise desired: Bioanalytical Services, Biology, Manufacturing/Production  
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.
 
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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Medical Director (9594) 

  Pharma job    All   5/5/2011 
Category: Management/Executive, Medical Management, Pharmacy/Pharmacology  
Education:   Position type: Full Time Executive  Experience: 5 years 
Area(s) of expertise desired:  
Description:
Responsibility for global medical affairs of marketed innovative product:
work with investigators, clinical associates, marketing and legal to ensure timely execution of phase IV clinical studies.
Development of global Key Opinion Leader relations.
Lead and/or support meeting and congresses, including medical congress symposia, expert meetings, advisory boards and internal meetings.
Preparation and/or review of Medical and Marketing materials.
Responses to medical questions from market.  
Requirements:
Requirements:
MD with 5-10 years of experience which includes experience in the pharmaceutical or Biotechnology Company.
Experience in a Global environment and/ or a previous similar role - a big advantage
Experience in leading clinical trials
MBA or business background - an advantage
Mother tongue level English
Excellent communication and presentation skills
Excellent analytical skills
Ability to work well in a global, complex, multi-interface structure  
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RA Project Manager 

  omrix    Tel Aviv Area, Nes-Ziona   8/8/2013 
Category: Biotechnology, Pharmacy/Pharmacology, Regulatory Affairs  
Education:   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Biology, GMP, Regulatory Affairs  
Description:
Omrix, a J&J Bio-Pharmaceutical company, is seeking RA Project Manager for its Nes-Ziona or Jerusalem Site. The position includes Providing Regulatory Affairs support, Generating and managing submission documents for new products or changes to existing files;
Assessing company activities, including new efforts and modifications for existing products, for regulatory impact and creating and executing regulatory strategies for implementation; Tracking requirements of regulatory agencies and implementing file updates accordingly.
 
Requirements:
Qualifications:
Degree in biology, chemistry, or another related field.
At least 2 years of Similar industry experience (QA / Medical Device) -
Experience in biologics Regulatory Affairs an advantage.
Familiarity with regulatory requirements
Working experience with regulatory authorities
Excellent communication, interpersonal and organization skills.
Computer skills: Microsoft Office applications.
Language: mother-tongue level English required

 
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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
 
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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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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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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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Job Offer in UK 

  LSC & Construction Engineer Ltd    All   28/6/2013 
Category: Engineering, Chemistry, Clerical/Administrative, Pharmacy/Pharmacology  
Education: Masters   Position type: Part Time  Experience: 3 years 
Area(s) of expertise desired:  
Description:
Engineers, Foremen, Captain, Mate Engineer, 2nd Engineer, 2nd/3rd Officer, Deckhand, Steward, Chef, Seafarers , Crew Job Seekers , Chief Engineer , Doctors, Nurses, Laborers, Pharmacists, Dentists, Masons, Plumbers, Drivers, Heavy equipment operators, architects, Surveyors, Customer Care Representatives.  
Requirements:
Certificates required  
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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

 
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Regulation of drug development 

  ISK Ltd    Jerusalem Area, Jerusalem   21/12/2009 
Category: Life Sciences, Clinical Research, Pharmacy/Pharmacology  
Education: Masters   Position type: Part Time  Experience: 1 year 
Area(s) of expertise desired: Clinical Research, Formulation, GLP, GMP, Pharmacokinetics, Pharmacology, Safety, Toxicology  
Description:
b"h

our company is engaged with anti cancer drug development and we are looking for a part time employee to be resposible for the regulatory affairs of the company BUT not a consultant  
Requirements:
b"h




we ask a regulatory person with 1-2 years of experience of work in the field that can work with our regulatory consultant  
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