When Every Moment Counts
We are an innovative biopharmaceutical company advancing long-acting, controlled release medicines that deliver therapy precisely at the site of care, addressing critical unmet needs across surgical, metabolic and other high-impact indications.

Patient-First Mindset
PolyPid develops targeted therapeutic solutions designed to improve patient outcomes through exceptional efficacy and safety.
Guided by an experienced, patient-focused leadership and scientific team, PolyPid is committed to advancing precision drug delivery, ensuring therapies are delivered exactly where they can provide the greatest clinical benefit.
A Remarkable Team

Dikla Czaczkes Akselbrad
Chief Executive Officer
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Ms. Dikla Czaczkes Akselbrad serves as the Chief Executive Officer of PolyPid after serving as the company’s EVP and CFO since 2017, leading the company’s initial public offering on the Nasdaq Global Market in June 2020. Dikla brings more than 20 years of experience leading life sciences companies through critical international strategic, financial and business transitions, including raising over $350 million in various forms in her prior executive roles. Before joining PolyPid in 2014, Dikla served as CFO of Compugen Ltd. (NASDAQ & TASE: CGEN) after serving as CFO of Packet Technologies Ltd., and an audit manager at Ernst & Young Israel. She received a B.A. in accounting and economics and an MBA from Tel-Aviv University, and is a certified public accountant in Israel.

Dalit Fellous Hazan
Deputy CEO,
EVP R&D, Clinical, and Regulatory Affairs
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Ms. Hazan brings over 25 years of expertise in the pharmaceutical industry, specializing in regulatory affairs and drug development. With a strong background in Research & Development, Clinical, and Regulatory Affairs, she has led successful regulatory meetings and submissions to the FDA, EMA, Health Canada, and other global health authorities. Ms. Hazan has a proven track record in overseeing clinical development and managing clinical studies. Prior to her current role, she held senior regulatory affairs positions at Teva Pharmaceuticals Ltd. She holds an M.Sc. in Physiology and Pharmacology from the Faculty of Medicine at Tel Aviv University and an Executive MBA from Bar Ilan University.

Ori Warshavsky
Chief Operating Officer - US
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Ori has over 15 years of international experience in the pharmaceuticals industry with experience ranging from corporate strategy and business development to marketing and market access. Prior to joining Polypid Ori spent 10 years at Teva Pharmaceuticals with his last role being Senior Director of Oncology Marketing where he led the launch of several oncology products. Earlier in his career Ori served as the Head of Market Access for Teva in Canada and as Chief of Staff to the CEO of Teva’s global generics business. Ori started his career as a biotech engineer both in Israel and the US.
Ori holds a B.Sc. degree in Biotechnology Engineering from the Ben-Gurion University and an MBA from Duke University’s Fuqua School of Business.

Jean-Marc Hagai, Pharm.D
Chief Commercial Officer
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Dr. Hagai is a seasoned Life Sciences executive with 20 years of successful track record in corporate Marketing & Business Development positions at various big pharma companies. Before joining Polypid, he served two years as VP Business development for Biotech Company at Aurum Ventures, the technology investment arm of Morris Kahn. Previously he held senior global positions at Teva Pharmaceuticals including Director of Global Strategic Marketing for innovative drugs in Multiple Sclerosis and Global head of Women’s Health Portfolio for EMIA-APAC region. Dr. Hagai holds a Pharm.D, is a Doctor in Clinical Biology and also holds a Master in Marketing (Paris V University).

Jonny Missulawin
Chief Financial Officer
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Mr. Missulawin has over 15 years’ experience in financial operations in Hi-Tech and biotechnology companies. Before joining Polypid, Mr. Missulawin was an audit Senior at Ernst & Young Israel. He holds an MBA from Tel Aviv University in financial management, a BA in accounting and Economics from Bar-Ilan University, and is a certified public accountant in Israel.

Tal Vilnai
General Counsel & Corporate Secretary
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Mr. Vilnai has over 20 years of legal experience in corporate law, commercial law, securities law and international business transactions. Prior to joining PolyPid, Mr. Vilnai served as Associate General Counsel of Ceragon Networks Ltd. (NASDAQ: CRNT). Before Ceragon, he served as Legal Counsel of Gilat Satellite Networks Ltd. (NASDAQ: GILT, TASE: GILT) and prior to Gilat, as General Counsel and Corporate Secretary of Runcom Technologies Ltd. Mr. Vilnai holds an LLB law degree from the Faculty of Law at the Tel Aviv University. He is licensed to practice law and is a member of the Israeli Bar.

Maria Rubin
EVP, Operations
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Ms. Rubin has over 17 years of leadership experience in the pharmaceutical and biotech industries, specializing in Operations and Quality. Prior to her current role Ms. Rubin served as Vice President of Quality Affairs at PolyPid.
Before joining PolyPid, Ms. Rubin spent 10 years at Teva Pharmaceuticals, where she held Quality Control Director position and other Quality managerial positions.
Ms. Rubin holds a B.Sc. in Drug Chemistry from Bar-Ilan University and an MBA from the Open University in Israel.

Rivi Lev-Ari
VP, Human Resources
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Ms. Lev-Ari has over 20 years of experience in the HR field. She has vast knowledge in all aspects of HR, with extensive expertise in the pharmaceutical and bio-tech industry. She has held senior positions in HR management, including building HR departments, strategic planning, recruitment, training, talent management, compensation, and benefits. Prior to joining PolyPid Ms. Lev-Ari held various positions as HR Manager at Teva Pharmaceuticals and Insight Pharmaceuticals. She holds a B.A. degree in Behavioral Science and an M.B.A., both from the College of Management Academic Studies (COLMAN).

Nurit Tweezer-Zaks, MD, MBA
Chief Medical Officer
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Dr. Nurit Tweezer-Zaks is a senior biopharmaceutical executive with over 20 years of leadership across global pharma, venture capital, and biotech. She spent more than a decade at Sanofi, where she held senior international roles including Global Medical Lead for Established Products and Senior Director of External Innovation, advancing global licensing, partnerships, and lifecycle management.
She later joined aMoon Venture Capital as Operating Partner and Chief Medical Officer, leading global innovation scouting, investment due diligence, and strategic support for portfolio companies. As CEO and CMO of MediCane Health, she advanced preclinical and clinical programs while driving corporate growth and partnerships.
Dr. Tweezer-Zaks began her career as an internist and rheumatologist following a fellowship at the U.S. National Institutes of Health (NIAMS). She earned her MD summa cum laude from Ben Gurion University and an MBA from the Kellogg-Recanati program of Northwestern and Tel Aviv Universities.Chief Medical Officer
Manufacturing at Scale
PolyPid operates an approximately 18,000 square-foot,
GMP-certified, state-of-the-art manufacturing facility designed to support the commercial-scale supply of D-PLEX100.
Featuring fully integrated, end-to-end production capabilities, advanced analytical systems, and strict regulatory compliance, the facility ensures consistent product quality, operational reliability, and readiness for global commercialization.
Open Positions
QA Operation (Batch Release)
We are looking for an experienced QA Operation (Batch Release) professional to support GMP quality operations and batch release activities in a sterile manufacturing environment, ensuring compliant documentation and timely quality review.
QA Production Oversight
We are looking for a hands-on QA Production Oversight professional to provide real-time GMP oversight on the production floor in a sterile manufacturing environment, ensuring compliant execution of sterile production activities and timely escalation of quality risks.
Supply Chain Planer
The Supply Chain Planer will support planning, purchasing, inventory control, and day-to-day operational follow-up in a GMP pharmaceutical environment, ensuring material availability and coordinating interfaces to support timely production, testing, release, and supply activities.
Validation & Projects Engineer
A pharmaceutical company located in Petah Tikva is seeking a Validation & Projects Engineer, responsible for executing validation activities for equipment, systems and manufacturing processes in accordance with regulatory requirements, and leading engineering projects from planning through implementation.
Analytical R&D Lead
We are seeking a highly motivated and experienced Analytical R&D Lead to join our R&D department. This is a unique opportunity to play a leading role in the development of innovative pharmaceutical products throughout the entire product lifecycle, from early research through scale-up, regulatory submissions and commercialization. The successful candidate will lead analytical development activities in the R&D, collaborate closely with multidisciplinary teams, and drive solutions to scientific and technical challenges that support studies for both commercial and pipeline products.
מומחה GMP למחלקת האחזקה
למחלקת האחזקה במפעל תרופות סטרילי דרוש/ה Maintenance GMP Compliance Specialist, שיוביל/תוביל את תחום ה-GMP, הציות והאיכות במחלקת האחזקה ויהווה/תהווה גורם מקצועי מרכזי בהבטחת עמידת פעילויות האחזקה, הציוד והמערכות בדרישות האיכות והרגולציה.
Visual Inspector – בודק/ת ויזואלי/ת למוצר סטרילי
הבודק/ת הוויזואלי/ת יהיה/תהיה אחראי/ת לביצוע בדיקה ויזואלית של מוצר סטרילי, בהתאם לנהלי החברה, דרישות GMP וקריטריוני קבלה ודחייה מוגדרים, במטרה להבטיח את איכות המוצר ובטיחות המטופל.
אנליטיקאי/ת למעבדת QC
לחברה פארמצבטית באזור המרכז דרוש/ה אנליטיקאי/ת למעבדת QC לביצוע בדיקות אנליטיות ופיסיקליות עבור תוצרת גמורה, חומרי גלם וחומרי אריזה, אישור העבודות וטיפול ברשומות איכות.
דוגם/ת ניטור סביבתי לחדרים נקיים
התפקיד כולל ביצוע ניטור סביבתי שגרתי ובמהלך פעילות ייצור בחדרים נקיים, לרבות דיגום אוויר מיקרוביאלי, חלקיקים, משטחים וכפפות/ביגוד עובדים, בהתאם לתוכנית הניטור ונהלי GMP.
מהנדס/ת ולידציה ופרויקטים
לחברת פארמה הממוקמת בפתח תקווה דרוש/ה מהנדס/ת ולידציה ופרויקטים, אחראי/ת על ביצוע ולידציות לציוד, מערכות ותהליכי ייצור בהתאם לדרישות רגולציה, והובלת פרויקטים הנדסיים משלב התכנון ועד ההטמעה.
מפעיל למחלקת הייצור
העבודה כוללת הטמעה של תהליך ייצור במתקן חדש בחדרים נקיים (Grade A/B), חלק פעיל בהגדרת תהליכים תפעוליים, הגדרה ועדכון של נהלים, ופעילויות ניקיון, הכנה לייצור, ניטור סביבתי ובדיקה ויזואלית.
עובד כללי בחדרים נקיים
אחריות על ניקיון וחיטוי שוטף של אזורי ייצור וחדרים נקיים בהתאם לנהלי החברה ולדרישות GMP, לשמירה על סביבת עבודה סטרילית ומבוקרת והבטחת איכות המוצר.
ראש צוות ייצור סטרילי – מוביל/ת פעילות ייצור
הובלת הפעילות השוטפת ברצפת הייצור במפעל סטרילי, תוך שמירה על סטנדרטים גבוהים של איכות, בטיחות ועמידה בדרישות GMP, וניהול מקצועי של צוות המפעילים.
איש/ת מכשור ובקרה
למחלקת האחזקה דרוש/ה איש/ת מכשור ובקרה- Instrumentation and control technician אחריות מקצועית על תחום הבקרה בחברה.


