• At least 3 years experience as a scientific project manager in a biotech or pharmaceutical company
• Proven experience in leading pre clinical activities including animal models of infectious or inflammatory diseases.
• Experience in in-vitro models including assay development is a plus
• Experience working in international environment
• Ability to lead multiple scientific projects in parallel
• Creative thinking
• Ability to present scientific data at meetings
• Excellent communication skills: verbal and writing
• Must be fluent in English
• Background education: Ph. D degree in life sciences

Please contact Dan Teleman at dant@atoxbio.com

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For applications, please send your CV to jobs@evogene.com.

Please state the position’s reference number in the e-mail’s ‘subject’ li

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For applications, please send your CV to jobs@evogene.com.

Please state the position’s reference number in the e-mail’s ‘subject’ li.

VP operations Job description
Purpose:
Responsible for operations and manufacturing processes

Location:
Manufacturing facility at Yessod Hama’ala, headquarters in Ness Ziona

Responsibilities:
Manages manufacturing activities on-site and external sites
Ensure compliance of manufacturing activities with standards and company objectives
Plans, manages and execute CollPlant’s manufacturing workplans
Ensures the timeliness and quality of deliverables in accordance with SOPs and local regulations
Implements manufacturing processes, control systems and documentation
Drives continuous improvements of manufacturing processes, including yield improvement and cost reduction
Identifies opportunities and best practices contributing to operational effectiveness
Manages supply chain, purchasing and inventory
Provides a single point of contact for interfacing groups

Basic Qualifications:
MSc or PhD in Biotechnology or Chemical Engineering
Ten years experience in the pharmaceutical or medical device industry, and at least three years of management experience
Experienced in working under GMP conditions
Experienced in design and construction of production lines, including clean rooms
Operational performance measurement experience
International collaboration experience

alona@collplant.com

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Apply @: www.teva.co.il/careers, position no. 3189 or send your CV to: orna.porat-berger@teva.co.il

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Biologist/Immunologist for QC (Job no. TSX 0003)

For a biopharmaceutical company in Ramat Gan, a biologist/immunologist for QC is needed

• In process testing
• Analytical chemistry tests
• Protein and Buffer testing

Qualifications:
• M.Sc. in Biology/Biochemistry
• Experience in QC Lab work
• Experience and knowledge in a GMP surrounding

Please send resume to Rachel.Schecter@managingprosolutions.com and include job number.

Final Product Release Specialist (Job no. TSX 0008)

For a biopharmaceutical company in Ramat Gan, a Final Product Release Specialist is needed.

The Final Product Release Specialist is responsible for all tasks relating to the biological product which include:
• Building Batch Release Protocols for each Product and market according to each country’s requirements
• Compiling and creating the documentation that accompanies batch release; completing release forms, declarations.
• Review of final product batch files (collecting documents, reviewing charts and worksheets, etc.)
• Conducting deviation and complaint investigations if needed and recording all relevant information in the databases
• Packaging procedures- Approval of packaging worksheets, assigning Expiry dates for final products, review and release of packaging files and following packaging plans.
• Management of the final products shipment including visual inspection of the final shipment, follow up at each destination, attending shipping coordination meetings
• Approving shipments for final release to market; checking data loggers.
• Updating protocols and procedures if required according to company changes or regulatory needs
• Maintaining compliance with post marketing requests from the various health authorities and maintaining compliance with the
• Quality Agreements per country.
• Duty by rotation in Packaging Dept- evening shifts.

Responsible for all tasks related to Medical Device Product Release which include:
• Review of final product batch files
• Review of sterilization documents.
• External interfaces with the device manufacturer and sterilization site.
• Final device shipment activities, including visual inspection of the final shipment.

Qualifications:
• Degree in life science preferable.
• Minimum of 3 years experience in a GMP environment
• Organization and administrative skills
• Good working knowledge of Microsoft Office applications
• Can work under pressure and adhere to deadlines
• Flexibility in working hours
• Good people skills –can work in a team or individually
• Excellent English is required

Please send resume to Rachel.Schecter@managingprosolutions.com and include job number.

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1. Knowledge/Educational Requirements
• Extensive knowledge of quality principles and requirements
• Good understanding of Medical Device Regulatory requirements
• Good understanding of general management techniques.
• Degree level with scientific and company management background.
• 3-5 years successfull experience in Medical Device companies

2. Skills and Abilities
• Able to think clearly in order to create systems.
• Able to communicate clearly to all levels of the organisation, and to suppliers, consultants, customers and external auditors/inspectors.
• Able to provide leadership to the whole company on all aspects of the Quality System.
• Excellent auditing skills.

alona@collplant.com

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Niti Surgical is looking for a Pre-Clinical Manager who will be planning &
conducting the company preclinical investigations
during the development stages of its future products
The candidate will have to evaluate the Biological activity of the company’s
devices, both in terms of safety & efficacy.
Responsibilities begin with establishing of the study protocol, continue with the
submission of preclinical trials applications,
through monitoring of the study conduct, and end with submitting the final study
report.

Job Requirements:

Life Sciences/MD/Veterinary – mandatory.
At least 5 years of experience in the medical device industry and/or academic
research with preclinical research – mandatory.
Experience in the outsourcing of preclinical studies including protocols, timelines
and milestones and the review of reports
to fit regulatory directions – mandatory.
Basic knowledge of GLP and international regulatory guidelines as they pertain to
preclinical trials.
Experience in the preparation of clinical trial applications- mandatory.
Data analysis capabilities.
“Hands on” and a team player personality.
Experience in establishing and monitoring budgets and contracts.

Please forward your CV’s to Biopharm@netvision.net.il

VP Chemistry, Manufacturing and Controls
Job Description :

• Development, implementation, ongoing operation and optimization of CMC and
leading the design and implementation of
an integrated CMC plan. Specifically ensuring the delivery of characterized test
article material for all preclinical studies,
clinical study drug for all clinical trials and all CMC information to be utilized in
the assembly of all required global regulatory
submissions.

• Assure complies with all aspects of a drug meaning production according to
cGMP and compliance with all relevant
regulatory guidelines (ICH, FDA, EMEA. e.t.c).
• Issue of SOPs’ relevant to handling and distribution of the drug product to clinical
sites and to the market.
• Understanding and ability to critically evaluate chemical process development;
drug substance GMP manufacturing; new
formulation development; drug product GMP manufacturing; the development of
analytical control strategies, methods and
validation protocols; development and execution of drug product and drug
substance stability protocols; setting of
specifications; review of stability data; setting study drug expiry and re-evaluation
dates; packaging, labeling and clinical
distribution.
• Ensure timely delivery of material for both toxicology and clinical studies
• Build, establish and communicate a network of CMC content experts and external
contract vendors of appropriate quality
and technical capability

Job Requirements :

• Advanced graduate degree (MS or Ph.D.) in Chemistry related sciences, e.g.,
organic synthetic chemistry, medicinal
chemistry, analytical chemistry, pharmaceutical Sciences or Engineering
• Demonstrated leadership, preferably in more than one related CMC area.
Experience in multiple disciplines of drug
development is required (biologics, drug substance, manufacturing, analytical,
quality, formulation, shipping, labeling and
storage) and experience in drug development with many molecules of varying
degrees of complexity.
• Extensive experience in cGMP related CMC drug development or manufacturing.
• The candidate must have experience in the preparation of CMC regulatory
documentation.
• Strong teamwork/interpersonal skills and a demonstrated ability to influence at
many levels across many disciplines, both
externally and internally.
• Strong communication skills
• Demonstrated project management skills

Please forward your CV’s to Biopharm@netvision.net.il

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Please send cv’s (as Word documents) to Rachel.Schecter@Managingprosolutions.com

Teva Pharmaceutical Industries is looking for an Inhalers QA Section Manager

השתלבות בצוות הקמת מערך האיכות של יחידת המשאפים.
תחום שטח – פעילויות שוטפות במחלקה הכוללות: ביקורות בייצור ובאריזה, עבודה לפי כללי GMP.
בדיקת תיקי אצווה – בדיקת תיקי יצור ותיקי אריזה ושחרור אצוות
בקרה שוטפת בנושא מערכות קריטיות – בדיקה ואישור נתוני ניטור של מערכות קריטיות בייצור ואריזה

דרישות התפקיד:
תואר ראשון בכימיה/רוקחות/ הנדסת כימיה/ ביוטכנולוגיה/ביולוגיה/מזון – חובה
יתרון משמעותי למועמד/ת בעל/ת ניסיון באבטחת איכות מפעלית
התפקיד משלב עבודת שטח עם עבודה משרדית מרובה
נדרשת שליטה בישומי מחשב
אנגלית ברמה טובה מאוד

Apply @ www.teva.co.il/careers or send your CV to: moran.shiri@teva.co.il

A High tech company in the north of israel requires Production Plant manager Hebrew- must לחברת הייטק באזור הצפון דרוש\ה מנהל\ת מפעל יצור
דרישות:
” מהנדס\ת תעו”ן\אלקטרוניקה\מכניקה- חובה

” לפחות 3 שנות נסיון בניהול מפעל יצור בהייטק- חובה

” נסיון בניהול קו יצור של חברה המציירת מוצרים צבאיים\לחברות בטחוניות- חובה ללא פשרות

” נסיון בניהול מפעל יצור של 50 איש ומעלה- חובה

* נסיון מחברות בעלות מוצרים רב תחומיים משולבי אופטיקה- יתרון

” מגורים באזור הצפון – חובה (נכונות למעבר מגורים יש לציין על גבי קורות החיים)

* מייל jobs@esr.co.il

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The Job require some travel abroad for training
Please send your resume to hagai@iner-tech.com

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Position requires extensive, overnight travel up to 80%.

Please send your CV to: leanneg@netvision.net.il

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