Quality Control Inspector

Description

At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?

There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.

Job Summary

In this role, you will be responsible to handle raw materials acceptance activities, NCM reports related to raw materials, write and update procedures and forms related to incoming inspection. Adhering to Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) is essential to maintain all documentation necessary to ensure conformity to specifications and traceability of records.

Essential Duties And Responsibilities

• Responsible for raw materials acceptance activities in ERP/SAP, including approval of acceptance records generated by incoming inspectors and issuance of Certificate of Compliance for approved raw material.
• Responsible to verify that all acceptance test results follow GMP and GDP guidelines.
• Responsible for handling of all related incoming inspection non-conforming materials (NCM) – opening and supplying relevant data for occurred deviation.
• Responsible to write and update incoming inspection Forms and procedures.
• Responsible for the approval of all graphic and label related raw material.
• Responsible for the approval of Line clearance performed by quality inspectors.
• Assist with Changes (ECO) to improve or clarify established procedures.
• Provide a “Customer Service” attitude when interacting with internal and external
• customers while accomplishing work, production, and achieving quality standards.
• Conform with and abide by all regulations, policies, work procedures, instruction, and safety rules.
• Exhibit regular, reliable, and punctual attendance.
• Perform other duties as assigned based on business needs.
• Manufacturing Quality Stamp number – MQ8
  
  

Basic Qualifications

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

Preferred Knowledge, Languages, Skills And Abilities

• Able to be aware of all relevant standard operating procedures as per Company policy as they are related to the position covered by this Job Description
• Support and contribute to Lean Sigma programs and activities towards delivery of the set target
• Able to comply with the company’s safety policy at all times
• Able to comply with the company’s quality policy at all times.
• Ability to work under pressure
• Good interrelation skills
• Technical ability - ability to read technical drawings
• Creativity
• High Learning ability
• Organized
• Ability to prioritize
• Excel - basic knowledge and experience.
• Written and verbal communication skills: Hebrew - Mother tongue. English - Good
• 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
  
  

Physical & Mental Requirements

• Very Heavy/ Heavy/ Medium/ Light/ Sedentary: _____Light_______
• List any mental requirements:
  
  

Competencies/Authorities

• Approval / Rejection of raw material
• Handling of NCM reports
• Sending COC for released raw materials
• Release raw materials in ERP system
• Update Procedure / Forms related to Incoming Inspection
  
  

Delegation/s (Title)

Manufacturing Quality Auditor or Qualified person

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com . Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre-employment drug screening.