Senior Quality Assurance Specialist (Filtration)
SGS North America Inc.

Grass Lake, Michigan

This job has expired.


Company Description

SGS is the global leader and innovator in inspection, verification, testing and certification services. Founded in 1878, SGS is recognized as the global benchmark in quality and integrity. With over 97,000 employees in 130 countries and operating a network of more than 2,400 offices and laboratories, we provide services to almost every industry by assuring quality and safety of products and services.
Trusted all over the world, SGS is a market leader because we put 100% passion, pride and innovation into everything we do. We encourage new ideas. We welcome people who challenge the way we do things. And we will be 100% committed to helping you reach your full potential.

Job Description

As the Quality Assurance Specialist, you will develop, promotes, maintains, and improves the local Quality, HSE, and OI Systems. Actively communicates the elements and values of the Systems to clients as well as employees.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Writes, revises, and edits facility quality documents to make them consistent and compliant with the SGS HSE, OI, and Quality Systems, accreditation body/regulatory requirements, and satisfactory for customers and auditors.
  • Has responsibility and authority for assuring the SGS-IBR HSE, OI, and Quality Systems are implemented, maintained and continuously improved. Ensures the SGS-IBR Quality System meets accreditation and certification requirements.
  • Performs and oversees internal auditing; reports findings during Management Review. Catalyzes, documents, and maintains the Corrective Action systems.
  • Serves as the principal contact with external auditors.
  • Assures personnel are aware of the relevance and importance of their work, and how it relates to SGS-IBR HSE, OI, and Quality Objectives. Coordinates training of staff on SGS-IBR's quality system.
  • Responsible for local facility's Approved Vendor List and Document Control System. Provides guidance to the Document Control Coordinator as needed.
  • Responsible for maintaining a program and procedures for the calibration/maintenance/verification system.
  • Serves as an internal resource for requirements of the quality system and 3rd party/regulatory compliance.
  • Support local and corporate HSE, OI, QHSE responsibilities, including involvement in risk assessment as required, ensuring that HSE, OI, and QHSE requirements are followed where relevant.
  • May require administrative duties to be performed at the request of the department managers.
  • May require basic laboratory duties to be performed at the request of the lab managers.
  • Perform errands and deliveries as assigned, including purchasing lab supplies, etc.
  • Adheres to internal standards, policies and procedures.
  • Performs other duties as assigned.


Qualifications

Required:
  • BS degree in Chemistry, Biology, or related sciences.
  • 3 plus years of experience in a regulated commercial lab environment.
  • Knowledge of scientific principles and Good Clinical Practice (GCP).
Preferred:
  • Certified Quality Auditor (CQA) or Certified Quality Manager (CQM) certification (RAB or ASQ)
  • Excellent interpersonal, communication (written and verbal), and organizational skills in combination with independent thought and proven problem-solving abilities.
  • Persuasive, diplomatic, but always to the point, and a strong ability to sell a concept.
  • Hands-on, open-minded, proactive team player.
  • Strong leadership skills.
  • Highly motivated, dependable, and detail-oriented.
  • Capable of building trust, value, and effectivecommunication.
  • High integrity, excellent work ethic.
  • Self-managed and responsible for project and time management.



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