Regulatory Affairs Coordinator

אודות חברת פיברו בריאות בעלי חיים

חברת פיברו בריאות בעלי חיים הינה חברה בינלאומית בבעלות ציבורית בעלת פעילות ענפה של למעלה ממאה שנים בייצור בגלובלי של תוספי מזון רפואיים, תרכיבים ותרופות ומספקת פתרונות ייחודיים מתקדמים לענף החי ברחבי העולם. הפעילות של פיברו נאמדת בכמעל 820 מיליון דולר. פיברו מעסיקה למעלה מ-1500 עובדים ברחבי העולם.

Phibro seeking a RA Coordinator, for our Beit Shemesh site in Israel.

This an opportunity to join a global team, Reporting to Global RA Vaccines Product Director

Phibro Animal Health Corporation is a publicly traded organization with a rich history spanning nearly 100 years of service. The Company is a global manufacturer of medicated feed additives, feed ingredients, advanced nutrition solutions, vaccines, and specialty chemicals for various industrial markets. Phibro’s revenues are more than $820 million and are supported by over 1500 employees worldwide.

The Regulatory Affairs Coordinator is an integral part of Global Regulatory Affairs team.

Responsibilities:

• Update and maintain databases to ensure information is accurate, renewal dates are known and planned, and information is readily communicated to all interested parties.
• Archive in accurate and timely manner the regulatory documents.
• Update regulatory documentation following issue of licenses.
• Prepare the Quarterly regulatory activities report.
• Ensure national requirements are communicated to global regulatory affairs.
• Remain aware of current regulatory environment and, where affected, ensure the business complies.
• In this Position, the Regulatory Affairs coordinator will coordinate the Artwork activities,
• Plan and execute artwork change and align with manufacturing production schedules to maximize impact of new packaging introduction and minimize packaging write off costs. Ensure artwork changes following license renewals and variations are made in line with published timelines. Maintain adequate processes to ensure monitoring of artwork changes.
  
  

• Bachelor’s degree Biology, Chemistry, or other equivalent qualifications,
• 1-2 years pharmaceutical industry experience,
• Regulatory affairs experience would be ideal,
• IT literate. Able to use standard business software, communication tools and documents management systems.
• Graphic design knowledge would be ideal.
• Analytically minded with strong attention to detail and problem-solving skills
• Experience in managing an international relationship and across geographic, time zones and different cultures.
  
  

• Hebrew (Highly Advantage)
• High English required.
• Additional languages a plus