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.
אוניפארם בע"מ
- מספר מקומות
-
אוניפארם בע"מ
- מספר מקומות
-
מלאה
-
Key Responsibilities:
Ensure compliance with regulatory and quality standards.
Review and write key documentation, including SOPs, specifications, operating procedures, templates, and forms
Manage quality events, laboratory deviations (OOS/OOT/OOE), and root cause analyses.
Conduct risk assessments and implement process improvements.
Oversee CAPAs, Change Controls, and training programs.
Lead stability programs to ensure product quality and compliance.
Support internal and external audits.
Approve and validate analytical methods, including method validation, verification, and transfers.
Collaborate with R D on new product development and method optimization.
Ensure compliance with regulatory and quality standards.
Review and write key documentation, including SOPs, specifications, operating procedures, templates, and forms
Manage quality events, laboratory deviations (OOS/OOT/OOE), and root cause analyses.
Conduct risk assessments and implement process improvements.
Oversee CAPAs, Change Controls, and training programs.
Lead stability programs to ensure product quality and compliance.
Support internal and external audits.
Approve and validate analytical methods, including method validation, verification, and transfers.
Collaborate with R D on new product development and method optimization.
Requirements:
Qualifications:
B.Sc. in Life Sciences, Chemistry, Chemical or Biotechnology Engineering (mandatory).
1-3 years of hands-on experience in a pharmaceutical QC lab (mandatory).
Strong analytical, problem-solving, and multitasking skills.
Ability to work under pressure and meet tight deadlines.
Excellent communication skills; fluency in Hebrew English (reading writing).
Experience in analytical method validation, verification, and tech-transfer a significant advantage
Previous experience in pharmaceutical QA Laboratory or QA Compliance roles a significant advantage
Qualifications:
B.Sc. in Life Sciences, Chemistry, Chemical or Biotechnology Engineering (mandatory).
1-3 years of hands-on experience in a pharmaceutical QC lab (mandatory).
Strong analytical, problem-solving, and multitasking skills.
Ability to work under pressure and meet tight deadlines.
Excellent communication skills; fluency in Hebrew English (reading writing).
Experience in analytical method validation, verification, and tech-transfer a significant advantage
Previous experience in pharmaceutical QA Laboratory or QA Compliance roles a significant advantage
This position is open to all candidates.
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.
אונליין
אונליין
תעודה ממשלתית
2 חודשים
סבסוד
