| |
|
|
|
|
 |
|
|
|
|
| לוח דרושים בתחומי
ביוטכנולוגיה, רוקחות, מדעי החיים, ציוד רפואי וקלינטק |
|
|
|
|
|
|
|
|
 |
| |
|
ברוכים הבאים ל
BiotechJob!
|
לוח דרושים
BiotechJob.co.il יעזור לכם
למצוא עבודה ולהתקדם בקריירה. האתר מכיל מאגר משרות
מעודכנות של חברות המובילות בישראל בתחומי ביוטק ,פארמצבטיקה,
מדעי החיים, כימיה, ציוד רפואי ועוד בתחומים רבים. ניתן
לבצע חיפוש ולשלוח קורות חיים ישירות למעסיקים. אנו
ממשיכים בפיתוח האתר ובקרוב נוסיף אפשרויות נוספת לחיפוש
עבודה.
מאחלים לכם הצלחה,
צוות BiotechJob |
|
|
|
|
|
|
|
|
|
VP BD & Marketing |
|
|
| תחום: |
מנהלים /בכירים/ כספים, ציוד רפואי
|
|
|
השכלה: |
|
תפקיד: |
|
שנות ניסיון: |
יותר מ10 שנים |
היקף המשרה: |
מלאה |
|
|
ידע/ניסיון: |
Medical Device, Start-Up
|
|
|
תיאור: |
VP of BD & Marketing that will manage all activities in the areas of business
development and marketing in the company, achieve company’s goals and target and maximize shortand
long-term revenue streams fostering growth.
The VP BD & Marketing will define business strategies and priority segments, provide guidelines for
business development and marketing plans, lead collaboration & implementation efforts with strategic
players and be responsible for the top line revenue of the company.
Reports to the CEO.
Responsibilities
1. Manage all company resources and activities related to corporate development, business development
and marketing.
a. Analyze the different market sectors and trends within the Ultrasound and Ablation market segment
including Interventional Oncology, Electrophysiology, and Pain Management.
b. Map the value chain and ecosystem of clients, partners, and competitors in order to maximize
market opportunities.
c. Define business strategies, prioritize market segmentation, and provide guidelines for business
development and marketing plans.
i. Work closely with our business partners and KOL's from the medical sector to understand and
define the needs for full execution of a desired strategy.
d. Set targets for annual growth and prepare plans that maximize short- and long-term revenuegenerating
opportunities.
e. Develop and implement strategic and tactical processes that drive meaningful results from
Marketing and Sales activities.
2. Secure essential alliances with strategic partners, and establish [new] partnerships with imaging/ablation
manufacturers which lead to M&A.
a. Define and implement long-term goals designed to meet the company's strategic objectives.
b. Lead collaboration and implementation efforts with strategic partners.
c. Define a clear sales road map and create distribution channels for the company’s products.
|
|
|
דרישות: |
• 10+ years of experience in business development, in the Medtech field. (Experience in Medical
Imaging software – an advantage)
• Proven success in developing, structuring, negotiating and closing complex deals.
• Seasoned management professional with strong business development skills, corporate strategy and
marketing insight.
• Hands-on executer, with an attitude to attain the industry leadership needed to prepare the business for
growth.
• Excellent communication skills, with the capability of articulating the company’s ongoing strategic
product/market vision into sound operating business plans, processes and revenue.
• Strong leadership and influencing skills to effectively focus and motivate partners.
• Ability to travel
|
|
|
|
|
| |
|
|
סמנכ"ל פיתוח והנדסה |
|
|
| תחום: |
הנדסה, מנהלים /בכירים/ כספים, ציוד רפואי
|
|
|
השכלה: |
|
תפקיד: |
|
שנות ניסיון: |
10 שנים |
היקף המשרה: |
מלאה |
|
|
ידע/ניסיון: |
Engineering, Medical Device, Research, Start-Up
|
|
|
תיאור: |
חברת סטארט אפ העוסקת בפיתוח פרוצדורה רפואית פולשנית
התפקיד מחייב ניסיון עשיר בפיתוח מוצרים רפואיים פולשניים, עם יכולות טכניות, ניהוליות ובין אישיות גבוהות.
|
|
|
דרישות: |
השכלה מכאנית – חובה, תארים מתקדמים יתרון.
• מנהל עם נסיון קודם בתפקידי ניהול פיתוח והנדסה בחברות הזנק למכשור רפואי, ניסיון בניהול ישיר של 5 אנשי פיתוח + קבלני משנה ויצרנים.
• היכרות מעמיקה עם סביבת העבודה והממשקים בפרויקט פיתוח מוצר רפואי פולשני ( רגולציה, קליניקה, בקרת איכות ).
• ניסיון טכני בפיתוח מוצרים מולטידיסיפלינאריים ( מנגנונים מכאניים, פלסטיקה, הינע ובקרה )
• אנגלית מצוינת
|
|
|
|
|
| |
|
|
Senior Project Manager |
|
|
| תחום: |
הנדסה, מנהלים /בכירים/ כספים, ציוד רפואי
|
|
|
השכלה: |
|
תפקיד: |
|
שנות ניסיון: |
7 שנים |
היקף המשרה: |
מלאה |
|
|
ידע/ניסיון: |
Engineering, Medical Device, Project Management, Research, Start-Up
|
|
|
תיאור: |
As Senior Project Manager, you will bring strong practical
experience of project management in a rapidly evolving, cross-functional, highly regulated
environment. This role also requires strong cross-functional business acumen, including
technical, manufacturing, finance, quality, clinical, and regulatory-based knowledge.
Responsibilities:
• Overall responsibility of all technical aspects of the device: Design, development, prototype
manufacturing and assembly, test planning and conduction, documentation in DHF
• Developing and managing project plans: Scheduling, risks and mitigation, resourcing, budgeting
• Preparing, presenting and archiving all Design Control reviews and other deliverables to support
project objectives
• Championing continuous improvement: evaluating project for opportunities to improve
performance; continuously monitors risk and mitigates as appropriate
• Project administration – accounting activities associated with projects, including monthly
reporting as required for grants accounting and services billing
• Demonstrating excellent interpersonal and communication skills, in a persuasive and inspirational
style that is timely, proactive, concise, candid, accurate, and clear, with all projects’ members
[including OEMs]
|
|
|
דרישות: |
• A Bachelor's degree in a Mechanical OR Biomedical engineering OR equivalent work experience
(Required)
• A minimum of 5+ years of related work experience in the medical device field (Required)
• Demonstrated skills in managing medical device development projects to produce effective and
differentiated products meeting customer expectations and internal business goals (Required)
• Must have experience working through all aspects of medical device design/development
including design V&V and process validation/technology transfer (Required)
• Working knowledge of design controls regulatory requirements (US, EU, Other) and experience
defending product information or processes in a regulatory audit preferred
• Experience developing designs and testing via a phase-gate analysis (Concept, Feasibility,
Verification) using a risk-based approach compliant with 21CFR/ISO-13485
• Extensive knowhow in V&V procedures and QA materials: writing protocols and reports
• Familiarity with manufacturing technologies
• Proficient in CAD/Solid works
• Excellent time management and organizational skills
• Outstanding written and oral communication
|
|
|
|
|
| |
|
|
מהנדס פיתוח / ראש פרוייקט |
|
|
|
|
|
השכלה: |
|
תפקיד: |
|
שנות ניסיון: |
5 שנים |
היקף המשרה: |
מלאה |
|
|
ידע/ניסיון: |
Cardiology, Engineering, Medical Device, Research, Start-Up
|
|
|
תיאור: |
לחברת סטארט אפ המפתחת מכשור רפואי קרדיולוגי
להובלת פרוייקט הפיתוח החדש של החברה
עבודה כחלק מצוות הפיתוח של החברה, דיווח למנהל הפיתוח
|
|
|
דרישות: |
מהנדס מכונות - חובה, תואר שני יתרון
בעל 3-5 שנות ניסיון בפיתוח מכשור רפואי
ניסיון במכשור רפואי מכאני פולשני, עדיפות לתחומי הקרדיולוגיה והשתלים
שליטה מצוינת בסולידוורקס
מצטיין בלימודים / צבא / עבודה
אנגלית מצוינת
|
|
|
|
|
| |
|
|
| |
|
|
R&D Team Leader |
|
|
| תחום: |
הנדסה, מנהלים /בכירים/ כספים, ציוד רפואי
|
|
|
השכלה: |
|
תפקיד: |
|
שנות ניסיון: |
8 שנים |
היקף המשרה: |
מלאה |
|
|
ידע/ניסיון: |
Cardiology, Medical Device
|
|
|
תיאור: |
• Leads system oriented complex technical project
• Leading a team of engineers and technicians directly as well as cross functional
• Establishes and maintains team member and project stakeholder relationships, expectations, and communications. This includes Quality, Operations, Manufacturing and Regulatory
• Conduct pre-clinical trials
• Measures project performance using appropriate tools and techniques in order to monitor the progress of the project, identify and quantify variances, perform required corrective actions, and communicates to all stakeholders
|
|
|
דרישות: |
1. Bachelor’s degree in mechanical engineering – Must
2. Degree in Bio-Medical engineering – Advantage
3. Strong design capabilities, small mechanisms design
4. Fluent English (oral and written)
5. Fast execution, highly motivated team player.
6. Hands-on attitude
7. 10 – 16 years of experience in mechanical / system engineering R&D
8. Proven technical leadership of a medical device project
|
|
|
|
|
| |
|
|
Head of QA Department |
|
|
|
|
|
השכלה: |
|
תפקיד: |
|
שנות ניסיון: |
8 שנים |
היקף המשרה: |
מלאה |
|
|
ידע/ניסיון: |
Medical Device, Quality Assurance
|
|
|
תיאור: |
esponsible for maintaining and ensuring that the Company's Quality Management System complies with FDA, ISO 13485, MDR and international medical device regulatory requirements
Responsibilities
• Responsible for planning, developing, and executing quality assurance policies, programs, and initiatives
• Responsible for company’s product quality and reliability to meet or exceed customer expectations
• Effectively create and support process enhancement initiatives to maintain an environment of continuous improvement throughout the organization.
• Develop and monitor improvement programs aiming to reduce the number of defects and improve level of quality
• Review and analyze statistical data and recommend changes or quality controls to eliminate problems
• Responsible to provide quality training and guidance for company personnel
• Responsible for writing and/or guiding employees to write company procedures.
• Maintenance of QA system.
• Periodic reports to top management about quality issues and analysis MRB, CAPA, ECOs, internal and external audits, and product and process performance.
• Participating in MRB, CAPA, ECO committees.
• Responsible for customer complaint handling
• Responsible for internal audit program
• Establishment and control of product traceability system
• Ensures quality by planning, monitoring, and appraising job results
• Promotes communication between colleagues and other departments for the benefit of information flow and to curb any problems that arise
• Act as PRRC for quality related issues
• Maintaining professional and technical knowledge by attending educational workshops, reviewing professional publications, establishing personal networks, and participating in professional societies
• Manage QA Department
|
|
|
דרישות: |
• Bachelor’s degree
• Minimum of 10 years of relevant experience with 7+ years of managerial experience, or advanced degree with a minimum of 8 years of relevant experience with 7+ years of managerial experience
• Previous experience in the medical devices or life science and QA fields managements (management of QA systems, support submission of the Technical Files and FDA submissions).
• Progressive leadership experience in medical devices as Quality Site Leader
• Outstanding organizational and leadership abilities
• Excellent interpersonal and public speaking skills
• Capability to work with cross-functional teams
|
|
|
|
|
| |
|
|
Regulatory Affairs Specialist |
|
|
|
|
|
השכלה: |
|
תפקיד: |
|
שנות ניסיון: |
4 שנים |
היקף המשרה: |
מלאה |
|
|
ידע/ניסיון: |
Medical Affairs, Medical Device, Regulatory Affairs
|
|
|
תיאור: |
• Conducts 510(k) and CE Mark impact assessments for product changes.
• Co-authors 510(k) submissions and significant change notifications for product changes with moderate business impact.
• Maintains letter-to-file history and updates technical documentation as needed in support of product changes/life cycle management and post-market data.
• Monitors and coordinates maintenance of global product registrations, product regulatory certificates, business licenses (e.g. CDPH), and establishment registrations.
• Maintains regulatory databases such as FURLS, GUDID and EUDAMED to ensure data accuracy. • Ensures service continuity with key 3rd party regulatory services (e.g. contract regulatory representatives, standards maintenance service, etc.)
• Monitors product shipment eligibility based on market clearance/approvals as communicated by senior RA personnel.
• Coordinates notaries, legalizations, and apostilles in support of product registrations as needed. •
|
|
|
דרישות: |
• BA or BS degree required; science, technology, engineering and technology background highly preferred.
• Minimum 2 years of previous experience working in a regulated industry required; experience in the medical device field highly preferred.
• Minimum 2 year of regulatory affairs or regulatory compliance experience required.
• Familiarity with medical device regulations and standards (e.g. 21 CFR 820.30, ISO 13485, IEC 62304, ISO 14971, ISO 10993, etc.) preferred.
• Strong attention to detail, interpersonal skills, reading comprehension, organizational skills, multi-tasking, and critical thinking/problem-solving skills required.
• Experience with MS Word, MS Excel, and Adobe PDF to compile and publish documents required.
• Strong written and oral communication skills.
Compile and maintain regulatory documentation databases or systems.
Coordinate efforts associated with the preparation of regulatory documents or submissions.
|
|
|
|
|
| |
|
|
מנהל/ת שיווק גלובלי |
|
|
|
|
|
השכלה: |
Post-Bachelors, Pre-Masters |
תפקיד: |
|
שנות ניסיון: |
3 שנים |
היקף המשרה: |
מלאה |
|
|
ידע/ניסיון: |
Marketing, Nuclear Medicine, Sales
|
|
|
תיאור: |
שיווק המוצרים בטריטוריה עליה אחראי/ת.
איתור הזדמנויות ובניית צורך אצל הלקוח לשם הגדלת ההזמנות לחברה. סגירת הסכמים עם לקוחות פוטנציאלים.
ניהול בקרה תקציבית ויעדי מכירות.
תכנון אסטרטגי ארוך טווח של הפעילות העסקית והשיווקית של התחום.
בניית תוכניות עבודה שנתיות, הטמעתן ויישומן.
ניהול מערך תקשורת שיווקית ויחסי ציבור, ניהול כנסים, הכנת חומרי שיווק.
אחריות על תקציבים נרחבים בתחום. ניהול יחידת המכירות. העבודה כוללת ממשקי עבודה מטריציוניים מול מנהלי המטה ומנהלי היחידות של החברה.
|
|
|
דרישות: |
• תואר ראשון – חובה. העדפה לתואר במדעי החיים
• ניסיון קודם של כ-3 שנים בתחומי העיסוק של מפורטים
בתיאור המשרה- חובה
• ניסיון בתחום ניהול קמפיינים ומדיה דיגיטלית – יתרון
• ידיעת השפה האנגלית ברמה גבוהה - חובה.
• ניסיון בעבודה בשווקים בינלאומיים - יתרון.
• חשיבה מחוץ לקופסה, קריאטיביות ויצירתיות
• ניסיון בהשקת מוצרים בשוק הישראלי והבינלאומי - חובה!
• ניסיון עבודה עם קהלי מטרה B2B
• משרה כוללת נסיעות לחו"ל
• אחריות על אתר האינטרנט של החברה ואתרי המדיה החברתית
• כפיפות למנכ"ל החברה
|
|
|
|
|
| |
|
|
| |
|
|
Senior Protein Purification Scientist |
|
|
|
|
|
השכלה: |
Masters |
תפקיד: |
|
שנות ניסיון: |
6 שנים |
היקף המשרה: |
מלאה |
|
|
ידע/ניסיון: |
Academic, Biochemistry, Laboratory, Molecular Biology, Process Development, Project Management, Protein Chemistry, Research, Protein Purification
|
|
|
תיאור: |
Fantastic Farms is a fast-paced biotechnology-oriented food-tech company, working to change how humanity is making food. Fantastic Farms is a pioneer in the alternative proteins landscape, as we are harvesting the power of plants to produce animal proteins and use them to recreate dairy and eggs. We put our heart, soul, and skills into making a difference for people, animals and the planet.
This is a new role that requires someone highly-motivated, energetic and an excellent team player focused on creating disruptive technology in the lab. The work requires hands-on process development for protein extraction, purification and characterization from plants.
Working together to push the boundaries, we blend the best of our talents to unlock innovation. We welcome you to join us in our adventure. Location: Tel-Aviv.
|
|
|
דרישות: |
M.Sc or Ph.D. in Life Sciences/Chemistry/Biochemistry with at least 6 years of industry experience
Expertise in protein purification demonstrated through purification of several types of proteins using a wide range of methods for at least 4 years hands on experience
Ability to perform and interpret protein analytical assays such as SDS-Page, WB, ELISA, HPLC
Independently develop new purification protocols, identify and resolve product and production related issues
Self-starter and highly independent individual comfortable to work under pressure and deadlines
Passionate to perform cutting edge protein science, using advanced laboratory equipment
Flexibility to work varying schedules and hours as needed according to changing deadlines
Industrial experience and demonstrated success in process and product development, scale-up - advantage
Familiarity with ISO9000, or cGMPs - advantage
|
|
|
|
|
| |
|
|
Senior Protein Purification Scientist |
|
|
|
|
|
השכלה: |
Masters |
תפקיד: |
|
שנות ניסיון: |
6 שנים |
היקף המשרה: |
מלאה |
|
|
ידע/ניסיון: |
Academic, Biochemistry, Laboratory, Molecular Biology, Process Development, Project Management, Protein Chemistry, Research, Protein Purification
|
|
|
תיאור: |
Fantastic Farms is a fast-paced biotechnology-oriented food-tech company, working to change how humanity is making food. Fantastic Farms is a pioneer in the alternative proteins landscape, as we are harvesting the power of plants to produce animal proteins and use them to recreate dairy and eggs. We put our heart, soul, and skills into making a difference for people, animals and the planet.
This is a new role that requires someone highly-motivated, energetic and an excellent team player focused on creating disruptive technology in the lab. The work requires hands-on process development for protein extraction, purification and characterization from plants.
Working together to push the boundaries, we blend the best of our talents to unlock innovation. We welcome you to join us in our adventure. Location: Tel-Aviv.
|
|
|
דרישות: |
M.Sc or Ph.D. in Life Sciences/Chemistry/Biochemistry with at least 6 years of industry experience
Expertise in protein purification demonstrated through purification of several types of proteins using a wide range of methods for at least 4 years hands on experience
Ability to perform and interpret protein analytical assays such as SDS-Page, WB, ELISA, HPLC
Independently develop new purification protocols, identify and resolve product and production related issues
Self-starter and highly independent individual comfortable to work under pressure and deadlines
Passionate to perform cutting edge protein science, using advanced laboratory equipment
Flexibility to work varying schedules and hours as needed according to changing deadlines
Industrial experience and demonstrated success in process and product development, scale-up - advantage
Familiarity with ISO9000, or cGMPs - advantage
|
|
|
|
|
| |
|
|
|
| |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
 |
|
