Manager, QA (IC role)

10 years

0 Lacs

Posted:4 days ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Job Overview

Manages and ensures proper execution of the audit and inspection programs.

Summary Of Responsibilities

  • Oversees designated global audit programs for compliance with the master audit plan, (procedures, execution, QC, compliance to process, etc.)
  • Identifies the scope and leads global audits and associated audit team.
  • Facilitates prioritization of global projects for risk-based audits.
  • Ensure the consistent implementation, use and review of SOPs.
  • Escalate issues to management in a timely manner implementing appropriate solutions, including preventative actions.
  • Negotiate with functional and operational internal stakeholders to improve quality and increase efficiencies.
  • Analyze and interpret data to lead functional process improvement initiatives to drive efficiencies and effectiveness of Regulatory Compliance and Quality Assurance (RC and QA) processes.
  • Lead and effectively manage constructive crucial interactions with clients or regulatory agencies.
  • Lead functional process improvement initiatives to drive efficiencies and effectiveness of Regulatory Compliance and Quality Assurance (RC and QA) processes.
  • Interpret applicable quality regulations/standards and create appropriate policies and procedures.
  • Ensure Regulatory Compliance and Quality Assurance (RC and QA) management responsibilities, as indicated in applicable controlled documents, are followed.
  • All other duties as needed or assigned.

Qualifications (Minimum Required)

  • A minimum of a bachelor’s degree in Life Sciences preferred (or equivalent Life Science experience).
  • Experience may be substituted for education.

Experience (Minimum Required)

  • 10+ years of experience in regulatory environment (experience in GXP roles).
  • Experience in conducting GCP and GVP audits.
  • Experience and regulatory expertise of industry quality systems/standards.
  • Ability to interpret applicable regulations/standards.
  • Experience in leading process improvement initiatives.
  • Ability to communicate and negotiate with internal stakeholders effectively.

Preferred Qualifications Include

  • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Physical Demands/Work Environment

  • Some overtime required.
  • Travel may be required.
  • Office-Based (Hybrid), as requested by the line manager.
Learn more about our EEO & Accommodations request here.

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Fortrea

Pharmaceuticals

Durham

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