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Vice President of Quality

LTS Device Technologiesנתניה, מחוז המרכז, ישראללא צויןFull-timeדרגה: לא צוין

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תובנת Willbi
חובה
  • At least 10 years of work experience in the QA field
  • At least 5 years experience as a manager
  • Solid experience in ISO and external Audits
  • Experience in working with medical device standards
  • Quality systems management (QMS, CAPA, NCMR, ECO, SCAR, inspections, release)
יתרון
  • A degree in science / Engineering
  • Experience in working with manufacturing companies
  • Clean room and sterilization understanding
  • Experience in combination device field and working with Pharma companies

חולץ מתיאור המשרה · מתעדכן אוטומטית

תיאור המשרה המלא

המשרה המקורית · נשמר לעיון

VP QA

About us

LTS is a leading pharmaceutical technology company that develops and manufactures innovative drug delivery systems for the pharmaceutical industry.

LTS´ commercial offering encompasses more than 20 marketed products.

LTS operates today from 5 sites: Netanya (Israel), Adrenarche (Germany), West Caldwell (NJ, USA), St. Paul (MN, USA), and Shanghai (China).

About the role

We are looking for an excellent VP QA to join our team in Israel.

The position is permanent, full time, hybrid.

Responsibilities:

Managerial responsibilities:

· Part pf company’s Staff, reporting to GM.

· Manage QA’s short term and long term planning and activity

· Manage QA department

· Strategy building – 1 and 3 Years plan

· Manage QA budget

· Build quality monitors for the company management

Professional responsibilities:

· Responsible for managing quality systems, processes, and procedures to assure product quality and safety.

· Management representative for the company’s QMS

· Overview, follow up and guidance of routine QA/QC activities such as CAPA, NCMRs, ECO, SCAR (customer compliant), incoming inspection, in process inspection, final inspection, product release.

· Provide guidance to product development teams as to the required deliverables to ensure compliance throughout product development cycle.

· Responsible for engaging strong intradepartmental and cross-functional/organizational relationships to drive quality system requirements.

· Communication with regulatory and certification agencies

· Responsible for Internal audits and suppliers' audits, certify suppliers to required standards. Lead external audit preparation

Direct Manager: GM

Job Requirements:

• Education: A degree in science / Engineering – an advantage

• Job skills: At least 10 years of work experience in the QA field

• At least 5 years experience as a manager

• QA management experience in a medical device company – a must

• Solid experience in ISO and external Audits

• Experience in working with medical device standards

• Experience in working with manufacturing companies – an advantage

• Clean room and sterilization understanding –a n advantage

• Experience in combination device field and working with Pharma companies - an advantage

• Computer skills: Full control of all MS-Office applications

• Language skills: English (reading, writing, and speaking) at a high level - mandatory.

At LTS, we value collaboration, innovation, and accountability.

We're looking for individuals who can relate to:

• Teamwork: Collaborate effectively, embracing diverse perspectives.

• Customer Focus: Exceed internal and external customer needs.

• Innovation: Create new opportunities with enthusiasm.

• Accountability: Take ownership of challenges, uphold standards.

• Leadership: Motivate and develop talents,

אודות LTS Device Technologies
פרופיל החברה · בקרוב

ביקורות עובדים · בקרובעוד משרות ב-LTS Device Technologies

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דומות וקשורות
LTS Device Technologies
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