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West Pharma QC Inspector 
Israel, Center District, Raanana 
26103954

28.06.2024

Essential Duties and Responsibilities:

  1. Responsible to perform set-up, in-process dimensional and visual audits to ensure compliance to all specifications and DMR. Responsible to record all the test results and the activities in the relevant documents as part of the DHR
  2. Responsible to verify that all acceptance test results meet the requirements according to the procedures and specifications.
  3. Responsible to verify that all acceptance test results follow GMP and GDP guidelines. Conform with and abide by all regulations, policies, work procedures, instruction, and safety rules.
  4. Responsible for the approval of line clearance at the production lines, testing stations and cleanroom.
  5. Responsible for approving raw materials.
  6. Responsible to verify stored raw material, approved devices and subassemblies and rejected materials are identified and traceable as required in applicable procedures and specifications.
  7. Responsible for nonconformities handling inside the production room and for the MRB cage at Raanana warehouse.
  8. Responsible for incoming inspection for R&D items and materials that are in use to support devices samples build sand meet customer demands during development stages.
  9. Determine whether a Non-Conformance (NCR) has occurred and follow established procedures to initiate corrective actions.
  10. Perform other duties as assigned based on business needs.

Basic Qualifications:

  1. Education- Technical/ Practical Eng.- an advantage
  2. At least 2 years of relevant experience in Quality in the Medical Device/pharma industry
  3. Courses related to Medical Device regulation- an advantage
  4. Knowledge with ERP/ SAP- an advantage.

Preferred Knowledge, languages, Skills and Abilities:

  1. Ability to work under pressure
  2. Good interrelation skills
  3. Technical ability- ability to read technical drawings
  4. Creativity
  5. High Learning ability
  6. Organized
  7. Ability to prioritize
  8. Excel -basic knowledge and experience.
  9. Written and verbal communication skills: Hebrew- Mother tongue. English- Good
  10. Relevant work history and/or experience may be considered in lieu of degree

Travel Requirements:

  • Must be able to travel up to ____0___ % of the time

Competencies/Authorities

  1. Affix Approval / Rejection labels of raw material
  2. Approval the beginning of the production (FAI)
  3. Record and Handling of tests results In process and final reports
  4. Sending the final DHR to MQ Team leader
  5. Preparation of a sample of raw materials for incoming inspection tests
  6. Release raw materials from the MRB cage
  7. Approval of the line clearance
  8. Interim stop production

Physical & Mental Requirements:

  1. Very Heavy/ Heavy/ Medium/ Light/ Sedentary: ___________________

Delegation/s (Title):

Qualified personnel