עדיין מחפשים עבודה במנועי חיפוש? הגיע הזמן להשתדרג!
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
Phibro seeking a QA Operation referent, for our leading manufacturing site at Beit Shemesh. Reporting to QA team leader.
Phibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals.
Phibro is a diversified company. In addition to, animal nutrition and health, we manufacture and market products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets.
Phibro’s revenues are more than $1 billion and are supported by over 2,300 employees worldwide.
Essential Roles and Responsibilities:
• Ensure GMP compliance of Phibro to support manufacturing and commercial activities.
• Prepare, review, and approve documents related to the interfacing department (including SOPs, validation protocols and reports etc.)
• Provide on-the-floor or with camera aid of QA oversight for manufacturing activities, as needed.
• Review, assess and approval (if qualified) of investigations, risk assessments, change controls, deviations, and CAPA.
• Ensure that the manufacturing operators work according to regulatory guidelines and relevant procedures.
• Constant readiness for internal and external inspections.
•Review and approve of manufacturing batch records.
• Support on site and virtual audit activities, to ensure ongoing compliance.
Requirements:
- Bachelor's degree in biological / Biotechnology field
- 2-3 years of experience in the pharmaceutical industry- a must
- Direct knowledge and experience in process and/or Quality of manufacturing within a pharmaceutical GMP environment is desired.
- Additional experience in other areas of quality – Advantage Must be able to work under pressure and meet deadlines, while maintaining a positive attitude
- Knowledge of Quality Assurance requirements in local and EMA regions is required.
- Proficient in quality principles in a manufacturing facility.
- Proficient in root cause analysis and risk assessment methodologies
- Have good communication skills and able to work in collaboration.
- Effective time management; deliver results on time.
Excellent computer proficiency (MS Office – Word, Excel, Power Point and Outlook).
Has the ability to read, write and communicate in Hebrew and English.
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
משרות נוספות מומלצות עבורך
-
אחראי /ת QA - שוהם
-
שוהם
גבריאלה פושקין
-
-
QA - Priority Software Finance team
-
ראש העין
Priority Software
-
-
עובד/ת ה"א תפעול לחברת התרופות דקסל פארמה
-
אור עקיבא
דקסל פארמה
-
-
למערך האיכות דרוש/ה עובד/ת ה"א תפעול
-
חדרה
JobTime
-
-
למערך האיכות דרוש/ה אחראי/ת בקרות שינוי ומערכות ממוחשבות
-
חדרה
JobTime
-
-
QA Specialist – Pharmaceutical Industry
-
בית קמה
KAMADA
-
אונליין
אונליין