Image
You
Image
Including You

תוצאות חיפוש - Omrix Biopharmaceuticals

נמצא 12 תוצאות בקטגוריה "all"
בחרו את המשרות שאליהן תרצו לגשת על ידי סימון תיבה אחת או יותר בעמודה השמאלית
למידע נוסף על המשרות לחצו על שם המשרה
משרה
ascdescחברה
ascdescמיקום
בחירה
מיקום : תל השומר
בחירה
Utilities Team leader

Description

- Utilities Team leader (water, steam, condensed air, clean in place, HVAC and more)
- Personal responsibility for the water, steam, Clean In Place and condensed air systems
- Full responsibility on a team of engineers and validation engineers
- End to End project management (design, procurement, execution, and qualification, including documents writing) including new systems introduction, systems upgrade, energetic efficiency increase, cost saving.
- Problem solving and professional guidance to the engineers and validation engineers in the team
- Meeting all pharmaceutical quality and regulatory requirements
- Future upgrades road map creation including new technologies assessment
- Financial planning and execution
- Part of cross departments improvement in the plant

Requirements

o Engineering degree Bs.C in chemical/mechanical/Biotech or equivalent
o Proven people leadership skills
o Experience in the Pharmaceutical processes – regulations, quality requirements, change management, non-conformances, audits
o Experience of 6-8 years in the industry
o Professional knowledge in critical utilities (Water, steam, OFA) – advantage
- Reports to Engineering and validation department manager
- Primary location – PFI, Tel Hashomer

Location: תל השומר

Comments

Omrix is an equal opportunity employer promoting diversity and inclusion in the work place.
This position may be suitable for any person subject to their qualifications and capabilities, regardless of (inter alia) gender, origin, ethnicity, sexual orientation, and/or disability.
מיקום : נס ציונה
בחירה
Quality Systems Analyst

Description

• Full time employee, as part of the Omrix Change Admin Team
• Provide Quality Systems support for Document and Change Controls in Windchill Data Management System
• Training/Assisting Omrix users in using Windchill System
• Controlled Printing of Production Worksheets
• Support for Internal and External Audits

Requirements

Required Skills:
• High level of English - both reading and writing
• Proficient with computers and Microsoft Office programs (WORD and Excel)
• Able to work as part of a team and provide support to co-workers
• Ability to work under pressure and prioritize tasks
• GMP experience is an advantage

Location: נס ציונה

Comments

Omrix Biosurgery Israel is an equal opportunity employer promoting diversity and inclusion in the workplace.
This position may be suitable for any person subject to their qualifications and capabilities, regardless of (inter alia) gender, origin, ethnicity, sexual orientation, and/or disability.
יועצ/ת קליני/ת לחברות ג'ונסון & ג'ונסון ישראל

תאור המשרה

• מתן שירותי ייעוץ טלפוני קליני לרבות: ניהול מקרים של COVID-19, תאונות עבודה ומחלות תעסוקתיות.
• אחראי/ת לשמירה על עמידה בתקנות משרד הבריאות לרפואה תעסוקתית ותקני הבריאות של J&J.
• ביצוע הערכות בריאותיות כחלק ממדיניות קידום בריאות של החברה.
• תמיכה בפעילויות קידום בריאות שונות.
• עבודה מול מנהלים וריבוי ממשקים בארגון.
• עבודה מול ספק חיצוני בתחומי רפואה תעסוקתית.

דרישות וכישורים

• רישיון אח/ות מוסמך/ת בעל/ת תואר ראשון בסיעוד
• עדיפות לניסיון או תואר מוסמך בבריאות תעסוקתית
• ניסיון של 5 שנים כאח/ות
• מוסמך/ת החייאה
• יכולת עבודה טובה עם תוכנות Office השונות (Outlook, Word, Excel) - חובה, יתרון להכרות עם תוכנת Salesforce
• הכרות עם חוקים ותקנות הנוגעים לרפואה תעסוקתית – יתרון
• יכולת עבודה בצוות ותקשורת בינאישית ברמה גבוהה
• שפות -אנגלית ברמה גבוהה – חובה. רוסית / ערבית – יתרון

היקף משרה – 100%, משרה זמנית לחצי שנה עם אפשרות להארכה.
העסקה דרך חברת קבלן.
מקום עבודה עיקרי – עבודה מהבית במודל היברידי. נכונות ל-20% עבודה באתרי החברות השונים (צפון – יקנעם ועד מרכז – נס ציונה)

מיקום: כל הארץ

הערות

ג'ונסון & ג'ונסון הוא מעסיק המקדם שוויון הזדמנויות וגיוון במקום העבודה.
משרה זו עשויה להתאים לכל אדם באשר הוא בהתאם לכישוריו ויכולותיו, בין היתר, ללא קשר למגדר, מוצא, שיוך אתני, נטיה מינית ו/או מוגבלות.
מיקום : נס ציונה
בחירה
QA Engineer - Apex project (open for internal move)

Description

The project Quality Engineer is responsible for providing project support and applies professional quality engineering practices for process transfer and integrations of Global Surgery and Bio surgery product line to meet established project quality and financial objectives and serve as Quality Engineer for the Apex project, whose primary functions are:

• Achieve product quality systems goals/project goals
• Ensures compliance with company policies and procedures for Design Change Control, Process Change Control, Validation and Product/Process Transfers.
• Utilize process excellence tools/ methodology for continuous improvement and predictability.
• Provides guidance and quality support to project.
• Serve as QA Subject Matter Expert (SME) for the project.
• Review and Approval of project documents on behalf of Quality.
• Issue project Quality documents.
• Participate in root cause investigations.
• Participate in risk assessments processes related to the project.

Requirements

• A minimum of a Bachelor's Degree in Business, Science Related Field or Engineering is required. An advanced degree and/or MBA are a plus.
• A minimum of 3 years of broad-based technical/engineering/quality expertise in the medical device or pharmaceutical industry is required.
• Proficiency with engineering analysis and statistical software is an asset.
• Flexible and adaptable, capacity to work in a fast pace learning and complex environment is a must.
• Working knowledge of Medical Device Regulations, Directives and Applicable standards in the areas of Quality Systems and Vigilance is required.
• Knowledge of practices and policies of regulatory agencies required. Initiative in innovative approaches to Quality and Regulatory solutions and applications in a fast paced changing business environment.
• Experience working with multiple and matrix business functions (Operations, QA, etc.) is required.

Location: נס ציונה

מיקום : תל השומר
בחירה
Quality Engineer for external operations

Description

Scope:
Quality engineer for external manufacturing.

Responsibilities:
- Focal-point for Grifols external operations manufacturing processes
o Full responsibility on Use As Is (UAI) process:
Review Grifols process deviations
Provide comments and approve the disposition
Issue UAI form including mitigations according to Grifols assessment and technical assessment
o Perform risk assessment to Grifols NC in ETQ
o Participation in weekly meetings with Grifols, Omrix and Ethicon
o LYO release (batch files review, issue CoA's, CoC's, CBER)
o Review and approve shipment authorization forms

Requirements

Requirements:
- At least 3 years of experience in QA positions
- At least 3 years of experience in GMP environment
- English – high level
- People skills
- Multitasking skills

Location: תל השומר

Comments

Omrix Biosurgery Israel is an equal opportunity employer promoting diversity and inclusion in the workplace.
This position may be suitable for any person subject to their qualifications and capabilities, regardless of (inter alia) gender, origin, ethnicity, sexual orientation, and/or disability.
מיקום : תל השומר
בחירה
עובד/ת ייצור לאתר תל השומר

תאור המשרה

דרוש/ה עובד/ת ייצור לעבודת משמרות באומריקס תל השומר
במסגרת התפקיד:
עבודה בחדרים נקיים תחת כללי התנהגות ורגולציה מחמירים
עבודה כחלק מצוות
ביצוע ניקיונות של החדרים, הכלים וציוד ייצור
עבודה לפי נהלים והקפדה על תיעוד תקין של התהליך.
עבודה שוטפת עם ציוד ומסמכים בשפה האנגלית.
העבודה כוללת משמרות לילה, שישי בוקר ומוצ"ש – לפי הצורך
המשרה בהעסקה דרך חברת קבלן

דרישות וכישורים

ניסיון בעבודה בחדרים נקיים - יתרון
ידע בנהלי GMP- חובה
יכולות עבודה וניסיון ביישומי מחשב - חובה
אנגלית קריאה והבנה- חובה
עברית קריאה והבנה - חובה
יכולת הבנה טכנית
ראש גדול, חשיבה מחוץ לקופסא, יצירתיות, פרואקטיביות
יכולת עבודה ולמידה עצמאית

מיקום: תל השומר

הערות

אומריקס הוא מעסיק המקדם שוויון הזדמנויות וגיוון במקום העבודה.
משרה זו עשויה להתאים לכל אדם באשר הוא בהתאם לכישוריו ויכולותיו, בין היתר, ללא קשר למגדר, מוצא, שיוך אתני, נטיה מינית ו/או מוגבלות.

Quality Integration Leader (Open for Internal Move only)

Description

Quality integration lead: Plans, coordinates, and directs quality assurance programs designed to ensure continuous production of products consistent with established standards by performing the following duties personally or through subordinates. At this level, the position has a greater degree of impact on the business results and typically, responsibility for managing a group of professionals.

Requirements

•Quality Project management experience within J&J
•knowledge of Quality Engineering/scientific methods techniques and principles.
•Experience working in a medical device/pharmaceutical, regulated environment. This includes knowledge of, and experience with, applicable standards and regulations.
•Advanced technical understanding of manufacturing equipment and processes.
•Understanding of new product introduction processes, and expertise in process qualifications/validations.
•Experience managing projects, and demonstrating project leadership abilities.
•Strong mentoring, coaching, and leadership skills.
•Ability to lead & get things done through influence versus line responsibility
• Ability to collaborate and build strong partnerships internally/externally with customer focus

Location: נס ציונה

Comments

Johnson & Johnson is an equal opportunity employer promoting diversity and inclusion in the workplace. This position may be suitable for any person subject to their qualifications and capabilities, regardless of (inter alia) gender, origin, ethnicity, sexual orientation, and/or disability.
מיקום : נס ציונה
בחירה
מפעיל.ת ייצור לעבודה במשמרות

תאור המשרה

עבודה בחדרים נקיים תחת כללי התנהגות ורגולציה מחמירים
עבודה כחלק מצוות
ביצוע תהליכי ייצור של מוצרים סופיים ומוצרי בניים
ביצוע דיגומים מיקרוביאליים למערכות השונות
ביצוע ניקיונות של החדרים, הכלים וציוד ייצור
עבודה לפי נהלים והקפדה על תיעוד תקין של התהליך.
העבודה כרגע בשתי משמרות - בוקר וצהריים 7:00-16:00 / 14:00-23:00
+ שעות נוספות לפי הצורך
העבודה כוללת עבודה בימי שישי בוקר (ולעיתים גם מוצ"ש).
מתוכנן לעבור לעבודה בשלוש משמרות בשנה הבאה (2023) לרבות ימי שישי ומוצ"ש :
7:00-15:00 / 14:00-23:00 / 22:00-06:00

דרישות וכישורים

ניסיון בעבודה בחדרים נקיים (Grade C) – יתרון
ידע במוצרי MD - יתרון
ידע בנהלי GMP ו- GDP - יתרון
יכולות עבודה וניסיון ביישומי מחשב של אופיס (אקסל, וורד, פאוור פוינט) - חובה
אנגלית קריאה והבנה- חובה
עברית קריאה והבנה - חובה
ידע בפריוריטי – יתרון
יכולת הבנה טכנית
ראש גדול, חשיבה מחוץ לקופסא, יצירתיות, פרואקטיביות, תשומת לב לפרטים
יכולת עבודה ולמידה עצמאית

מיקום: נס ציונה

הערות

אומריקס הוא מעסיק המקדם שוויון הזדמנויות וגיוון במקום העבודה.
משרה זו עשויה להתאים לכל אדם באשר הוא בהתאם לכישוריו ויכולותיו, בין היתר, ללא קשר למגדר, מוצא, שיוך אתני, נטיה מינית ו/או מוגבלות.
מיקום : תל השומר
בחירה
Supply Chain Quality and Process Specialist

Description

Great opportunity to lead E2E supply chain quality and process improvements.
The position will let you explore, learn and experience supply chain operations under a Full GMP quality systems for medical device pharmaceutical combination product
Description
Supply chain is searching for Quality Specialist to support and lead quality systems and process improvement. Ensuring full alignment between working procedures and quality systems. Ownership of standardizations of logistics process.

RESPONSIBILITIES
• Responsible for all SC quality systems and processes within the sites.
• Ensures department quality & compliance with all regulations.
• Responsible for department audit readiness, including all preparations and changes required.
• Assist in supporting internal and third-party audits
• Supports Continuous Improvement and manage problem resolution
• Lead projects of process improvement
• Supports documentation and Quality Systems maintenance, including Non-conformance / Investigations, CAPA, Change Controls.
• Support improvement of working instructions and procedures.
• Cooperation with related departments

Requirements

• Bachelor’s Degree in life science/ quality engineering/ industrial engineer/ logistics or equivalent field - is advantage.
• Work Experience in manufacturing factories,
• Pharmaceutical industry or medical field- is advantage.
• Fast learner
• Experience in process and procedures writing.
• High computer orientation and proficiency (MS Office & Quality systems).
• Ability to follow directions and work independently and to carry out assignments to completion within parameters of instructions given, prescribed routines, and standard accepted practices while paying attention to detail
• Able to maintain 100% compliance in all SOP, cGMP, EHS and other training curriculum as assigned.
• Committed to follow company policies and procedures, follow cGMP and other regulatory requirements.
• Excellent verbal and written communication skills (Hebrew & English).
• English- Excellent verbal and written communication skills – a must.

Location: Nez Ziona (once a week in Tel Ashomer)
*Employment by a contracting company

Location: תל השומר

Comments

Omrix is an equal opportunity employer promoting diversity and inclusion in the workplace.
This position may be suitable for any person subject to their qualifications and capabilities, regardless of (inter alia) gender, origin, ethnicity, sexual orientation, and/or disability.
מיקום : נס ציונה
בחירה
Manager, Global Regulatory Affairs, CMC

Description

Ethicon, Inc., is recruiting for a Manager, Global Regulatory Affairs, CMC for the Ethicon Biosurgery Franchise. The position will focus on biologic products, drug products, and drug-device combination products and may be based at any J&J site. Preferred locations are the J&J sites located at Ness Ziona, Israel or Raritan, New Jersey, United States. Other J&J locations throughout the U.S. and Europe will be considered. Remote work options may be considered on a case-by-case basis and if approved by the Company.

Ethicon, part of the Johnson & Johnson Medical Devices Companies, has made significant contributions to surgery for more than 60 years from creating the first sutures, to revolutionizing surgery with minimally invasive procedures. Our continuing dedication to Shape the Future of Surgery is built on our commitment to help address the world's most pressing health care issues and improve and save more lives. Through Ethicon's surgical technologies and solutions including sutures, staplers, energy devices, trocars and hemostats and our commitment to treat serious medical conditions like obesity and cancer worldwide, we deliver innovation to make a life-changing impact. For more information, visit www.ethicon.com.

The Manager, Global Regulatory Affairs, CMC for Ethicon’s Biosurgery business unit will be responsible for leading a team of Regulatory professionals and partnering with R&D, Supply Chain, and other cross-functional team members and leaders to obtain and maintain Ethicon’s biologic, drug, and combination product portfolio globally through project team support, audit support, excellence in submission execution, global health authority interactions, and growing and developing talent.

The products supported by this position are regulated worldwide as biologics, drugs, or high-risk medical device (combination products) which are intended to address a range of surgical challenges related to bleeding and sealing. Primary responsibilities will include:

Key Responsibilities:
• Lead, inspire, motivate, and manage a team of Regulatory CMC professionals to obtain and maintain market access for Chemistry, Manufacturing, and Controls (CMC) related changes to Ethicon Biosurgery biologic, drug, and combination products. (Currently this position is responsible for managing 5 team members, which includes both permanent and contract staff.
• Mentor, coach, train, and develop technical and professional skills of the Regulatory CMC team.
• Maintain up-to-date understanding of global biologic, drug, and combination product regulations and guidance documents and advise Regulatory Affairs team and internal stakeholders on the interpretation and application of health authority expectations.
• Oversee assessment and communication of global CMC changes, strategies, risks, and requirements to internal business partners and leadership teams.
• Clearly and timely communicate compliance issues to Regulatory Management and business leadership that could affect registration or regulatory compliance.
• Active role on project teams to maintain close alignment between supply chain strategy and regulatory compliance and timelines.
• Oversee the strategy development, health authority negotiations, submission content, and post market commitments for U.S., EU, and Israel CMC-related regulatory filings.
• Partner with regional Regulatory leaders on regulatory strategy and submissions to successfully obtain and maintain marketing approvals for all other markets.
• Partner with external manufacturers and strategic external partners to communicate CMC changes, evaluate impact of changes, and ensure joint regulatory responsibilities are fulfilled and compliant.
• Lead Health Authority meetings for key markets and interact with Health Authorities regarding product regulatory filings.
• Evaluate the impact of current and emerging standards and regulations, assess the most effective and efficient strategies for obtaining or maintaining product registrations globally, and communicate changes and impact to cross-functional business partners.
• Demonstrate a deep scientific and technical understanding of products under the scope of responsibility to provide strategic guidance and support for product development and life-cycle management of products.
• Integrate changing, complex, and/or ambiguous information for effective decision-making and clearly communicate challenges and solutions to stakeholders to achieve strategic and/or project goals.
• Collaborate with Quality partners regarding product non-conformance and quality issues by contributing to internal investigation and risk management reviews.
• Manage, oversee, and balance resource allocation across critical projects.
• Influence and collaborate to bring about process and technical improvements within the organization.
• Manage front-room and back-room regulatory activities associated with internal and external audits.
• Ensure that company policies, procedures and practices are compliant with appropriate regulatory requirements.

Requirements

Education:
• Bachelor’s/undergraduate degree is required.
• Advanced degree is a plus.
• Degree in a technical related discipline (e.g. biological, pharmaceutical, or chemical sciences) is preferred.

Experience and Skills:
• A Bachelor's degree and at least 8 years of regulated healthcare industry experience, or an advanced degree and a minimum of 5 years of regulated healthcare industry experience is required.
• Previous experience with biologic or drug Regulatory Affairs is required.
• Previous experience with medical device and/or combination product regulatory affairs is preferred.
• Demonstrated track record representing your function on cross-functional or leadership teams is required.
• Previous experience developing and executing regulatory strategies that align with business deliverables is preferred.
• Previous experience leading, mentoring, coaching, or developing people or teams is required.
• Previous experience interacting with Health Authorities (for example: FDA, EMA, or other Health Authority meetings, negotiations, or audits) is required.

Job Requirements:
• High-level verbal and written communication skills is required.
• Up to 10% travel may be required. (Primary locations for travel may include Israel, Spain, Denmark, and New Jersey, USA.)

Location: נס ציונה

Comments

Johnson & Johnson is an equal opportunity employer promoting diversity and inclusion in the workplace.

This position may be suitable for any person subject to their qualifications and capabilities, regardless of (inter alia) gender, origin, ethnicity, sexual orientation, and/or disability.
מיקום : נס ציונה
בחירה
Associate Director, Global Regulatory Affairs, CMC

Description

Ethicon, Inc., is recruiting for an Associate Director, Global Regulatory Affairs, CMC for the Ethicon Biosurgery Franchise. The position will focus on biologic products, drug products, and drug-device combination products and may be based at any J&J site. Preferred locations are the J&J sites located at Ness Ziona, Israel or Raritan, New Jersey, United States. Other J&J locations throughout the U.S. and Europe will be considered. Remote work options may be considered on a case-by-case basis and if approved by the Company.

Ethicon, part of the Johnson & Johnson Medical Devices Companies, has made significant contributions to surgery for more than 60 years from creating the first sutures, to revolutionizing surgery with minimally invasive procedures. Our continuing dedication to Shape the Future of Surgery is built on our commitment to help address the world's most pressing health care issues and improve and save more lives. Through Ethicon's surgical technologies and solutions including sutures, staplers, energy devices, trocars and hemostats and our commitment to treat serious medical conditions like obesity and cancer worldwide, we deliver innovation to make a life-changing impact. For more information, visit www.ethicon.com.

The Associate Director, Global Regulatory Affairs, CMC for Ethicon’s Biosurgery business unit will be responsible for leading a team of Regulatory professionals and partnering with R&D, Supply Chain, and other cross-functional team members and leaders to obtain and maintain Ethicon’s biologic, drug, and combination product portfolio globally through strategy development, excellence in submission execution, global health authority interactions, internal and external policy shaping, and growing and developing talent.

The products supported by this position are regulated worldwide as biologics, drugs, or high-risk medical device (combination products) which are intended to address a range of surgical challenges related to bleeding and sealing. Primary responsibilities will include:

Key Responsibilities:
• Lead, inspire, motivate, and manage a team of Regulatory CMC professionals to obtain and maintain market access for Chemistry, Manufacturing, and Controls (CMC) related changes to Ethicon Biosurgery biologic, drug, and combination products. (Currently this position has 3 direct reports (2 permanent staff, 1 contract staff) and responsibility for an overall team of 12 individuals, including both permanent and contract staffing).
• Mentor, coach, train, and develop technical and professional skills of the Regulatory CMC team.
• Maintain up-to-date understanding of global biologic, drug, and combination product regulations and guidance documents and advise Regulatory Affairs team and internal stakeholders on the interpretation and application of health authority expectations.
• Oversee assessment and communication of global CMC changes, strategies, risks, and requirements to internal business partners and leadership teams.
• Clearly and timely communicate compliance issues to Regulatory Management and business leadership that could affect registration or regulatory compliance.
• Active role on various leadership teams, including Ethicon Biosurgery Regulatory leadership team and Supply Chain leadership teams to maintain close alignment between supply chain strategy and regulatory compliance and timelines.
• Oversee the strategy development, health authority negotiations, submission content, and post market commitments for U.S., EU, and Israel CMC-related regulatory filings.
• Partner with regional Regulatory leaders on regulatory strategy and submissions to successfully obtain and maintain marketing approvals for all other markets.
• Partner with external manufacturers and strategic external partners to communicate CMC changes, evaluate impact of changes, and ensure joint regulatory responsibilities are fulfilled and compliant.
• Lead Health Authority meetings for key markets and interact with Health Authorities regarding product regulatory filings.
• Partner with regional leaders and the Regulatory Affairs Policy Intelligence team to monitor the regulatory environment globally and assess and communicate the impact of current and emerging regulations on the company's portfolio of products, define the future vision, and drive innovative thinking.
• Evaluate the impact of current and emerging standards and regulations, assess the most effective and efficient strategies for obtaining or maintaining product registrations globally, and communicate changes and impact to cross-functional business partners.
• Demonstrate a deep scientific and technical understanding of products under the scope of responsibility to provide strategic guidance and support for product development and life-cycle management of products.
• Integrate changing, complex, and/or ambiguous information for effective decision-making and clearly communicate challenges and solutions to stakeholders to achieve strategic and/or project goals.
• Collaborate with Quality partners regarding product non-conformance and quality issues by contributing to internal investigation and risk management reviews.
• Manage, oversee, and balance resource allocation and budget across critical projects.
• Influence and collaborate to bring about process and technical improvements within the organization.
• Represent the company and influence regulations and health authority guidance through industry trade association(s) in partnership with the Policy Intelligence team.
• Ensure that company policies, procedures and practices are compliant with appropriate regulatory requirements.

Requirements

Education:
• Bachelor’s/undergraduate degree is required.
• Advanced degree is a plus.
• Degree in a technical related discipline (e.g. biological, pharmaceutical, or chemical sciences) is preferred.

Experience and Skills:
• A Bachelor's degree and at least 10 years of regulated healthcare industry experience, or an advanced degree and a minimum of 7 years of regulated healthcare industry experience is required.
• Previous experience with biologic or drug Regulatory Affairs is required.
• Previous experience with medical device and/or combination product regulatory affairs is preferred.
• Demonstrated track record representing your function on cross-functional or leadership teams is required.
• Previous experience developing and executing regulatory strategies that align with business deliverables is preferred.
• Previous experience leading, inspiring, and developing a team is required.
• Previous experience preparing for and/or participating in Health Authority meetings or negotiations (FDA, EMA and other health authorities) is required.
• Previous experience working with professional trade associations or external policy shaping is preferred.

Job Requirements:
• High-level verbal and written communication skills is required.
• Up to 10% travel is required. (Primary locations for travel may include Israel, Spain, Denmark, and New Jersey, USA.)

Location: נס ציונה

Comments

Johnson & Johnson is an equal opportunity employer promoting diversity and inclusion in the workplace.

This position may be suitable for any person subject to their qualifications and capabilities, regardless of (inter alia) gender, origin, ethnicity, sexual orientation, and/or disability.
מיקום : נס ציונה
בחירה
Assistant Controller

Description

Omrix Biopharmaceuticals, a Johnson & Johnson Company, is looking for a vital, dynamic, and reliable Assistant Controller

Main Responsibilities:
• Preparation of the statutory financial statements and tax return
• Taking part in the monthly and quarterly reporting in accordance with US GAAP
• Work closely with the Company's external auditors during financial and tax audits
• Responsible for tax reporting, collaborating with J&J Tax Corporate
• Leading SOX compliance and ensure proper implantation control processes
• Lease accounting calculations
• Ad-Hoc accounting and finance-related projects as needed

Requirements

• A Certified Public Accountant (CPA) with a BA in accounting/finance – a must
• Experience as an Assistant Controller from a global company – a big advantage
• Solid knowledge and experience with US GAAP and local taxation – a must
• Experience with SOX
• Strong English skills - both oral and written – a must
• Working knowledge of MS Office (especially Excel and PowerPoint)
• Ability to work under pressure in a multi-tasking environment and meet deadlines
• Attention to details and problem-solving ability

Location: נס ציונה

Comments

Omrix is an equal opportunity employer promoting diversity and inclusion in the work place.
This position may be suitable for any person subject to their qualifications and capabilities, regardless of (inter alia) gender, origin, ethnicity, sexual orientation, and/or disability.