Posted on: 10/5/2021

Job type: Permanent

Sector: Pharmaceutical and Healthcare

 
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The experienced Supplier Quality Manager (SQM) will work with our client's supplier for their BPS globally. The SQM will work to ensure suppliers, maintain a compliant quality system by abiding by internal requirements as well as ISO/GMP requirements.

Essential Duties and Responsibilities:

  • Responsibility for defined Supplier
  • Participates in the Supplier Selection process for the quality aspects
  • Responsible for qualifying or disqualifying suppliers, along with other involved departments
  • Contact person for site quality departments
  • Contributes to product development and product/component improvement projects/activities.
  • Manages the early involvement of suppliers and sets supplier requirements in line with quality and sustainability regulations and programs.
  • Drives PPAP/APQP or similar.
  • Responsible for the execution of supplier audit
  • Responsible for the audit planning, execution, preparation/issuance of audit reports and closure of audit observations.
  • Identify and conduct follow-up reviews to implement and validate corrective action plans.
  • Responsible for timely issuance of audit reports and closure of audit observations.
  • Responsible for Supplier Quality Assurance Agreements (SQAA)
  • Monitors and follows-up on the Supply Quality related KPI’s towards the suppliers
  • Drives and manages Supply non-conformance and complaint handling process, follow-up and resolution
  • Update global electronic data management system with all pertinent supplier information.
  • Effectively work with suppliers to improve processes and procedures related to quality.
  • Responsible for implementing functional processes/procedures
  • Performs other projects, tasks and responsibilities as assigned by the Manager of Supplier Qualification Management

 

Qualifications and Requirements:
Education:

  • Business Administration, Engineering, Chemistry, Biology or long-term experience in related fields

Experience:

  • A minimum of 5 years progressive experience in Pharma, Automotive or Aerospace Industry.
  • Experienced in electronic and/or mechanical processes
  • Certified Quality Auditor to ISO/GMP standards within the first two years
  • Experience in a Pharma Quality Environment Operational Excellence or similarly structured problem-solving.
  • Knowledge of ISO/GMP´s and familiar with pharmaceutical activities.
  • Experienced with regulatory requirements.
  • Expertise in using basic quality tools.
  • Good knowledge in office applications
  • SAP experience preferred.

License/Certification:

  • Certification as an auditor for ISO or GMP by a recognized organization within two years

Other Skills (ex. specific computer skills, level of oral/written communication, etc):

  • Excellent communication and presentation skills required.
  • High personal initiative and strong ability to motivate self and others.
  • up to 50% travel requirements.
  • Global work with multiple regions in the world.

Driving our future growth requires talented people. Our client is a dynamic organization suited to people who want to showcase skills, be recognized for expertise and thrive in a vibrant and innovative environment.


All qualified applicants will receive consideration for employment without regard to race, color, religion, sex or national origin.  We are also an equal opportunity employer of individuals with disabilities and protected veterans.

Contact

Nicole Obregon
00 52 55 1998 4000
Morgan Philips Group
Blvd. Miguel Cervantes Saavedra 169 - PH
11520 - CDMX Granada, Miguel Hidalgo
Mexico

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Reference: US833131
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