חזרה ללוח
יורוג'ן פארמה

Senior Manager, Quality Devices & Compliance

יורוג'ן פארמה

מיקום שרון
תחום פארמה
בכירות ביניים
היקף משרה משרה מלאה
גודל חברה גדולה (200+)
סוג תפקיד איכות

תיאור המשרה

Job Summary: Quality Devices: Leads all the quality aspects for medical devices development, manufacturing, release and life cycle management in accordance to regulatory requirements and UroGen Quality System requirements. Quality Compliance: Owner of Quality Management System (QMS), ensure compliance to regulatory requirements (cGMP/QSR/PQS/ISO13485) across the company and functions, lead and manage the Quality Compliance team. Duties & Responsibilities  Quality Devices  Ensure quality assurance support to development, production and product engineering of medical devices according to QSR/cGMP and ISO13485 requirements, regulations and guidelines for different markets.  Provide support to the medical devices Change Controls to ensure correct implementation of change control procedures pertaining to products, contract manufacturing and quality control facilities, etc.  Provide support in conducting quality audits of suppliers / vendors for medical devices, including as may be required raw material manufacturers, contract manufacturers, packaging materials manufacturers, contract laboratories etc. for the purpose of evaluation and approval.  Participate in preparation/review/approval of protocols and reports of studies pertaining to the drug or device products, the product transfer from R&D to manufacturing, the production processes, the equipment and systems of the manufacturing and quality control laboratories.  Quality Compliance  Owner of QMS and related processes, including CAPA, Deviations, Complaints, Risk Management, Audits (internal/external), Management Review, etc.  Provide support in training manufacturing, engineering, quality control and other personnel on the various relevant aspects of quality assurance.  Provide support in handling all customer complaint issues, including the complaint investigation, the reporting to regulatory authorities as required, feedback to the customer.  Lead and support quality improvement programs throughout the Company.  Perform any other related duties as management may require from time to time.

דרישות התפקיד

 At least 5 years of experience in medical devices industry (pharmaceutical and/or combination products experience is an advantage).  Management experience in Quality Assurance / Compliance in pharma/med.devices.  Knowledge and experience in medical device QSR (Pharmaceutical Quality Systems experience is an advantage).  Fluent in English.  Microsoft Office full proficiency (Word, Excel, Powerpoint).  Experience in technical and SOP writing.  Ability to view broad perspective of the organization's vision, objectives and interests.  Excellent interpersonal relations, ability to connect and work across the organization.  B.Sc./M.Sc. in Life Sciences or Technical sciences, or related studies or Pharmacist, with training in pharmaceutical quality assurance

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על ענף התעשייה: פארמה

תעשיית הפרמצבטיקה (פארמה) היא עמוד התווך של הרפואה המודרנית, העוסקת במחקר, פיתוח, ייצור ושיווק של תרופות למניעה וטיפול במחלות. חברות הפארמה פועלות תחת רגולציה קפדנית ביותר של גופים בינלאומיים כמו ה-FDA וה-EMA, במטרה להבטיח את בטיחותם ויעילותם של הטיפולים הרפואיים. תחום זה דורש שילוב הדוק בין מדענים, קלינאים, אנשי רגולציה ואבטחת איכות, ומציע מגוון רחב של קריירות יציבות ובעלות השפעה מצילת חיים.

מודעה Bio4Bio
מודעה Scout-Jobs