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GxP Consultant

Azzur Group

Los Angeles, california


Job Details

Not Specified


Full Job Description

Azzur Group is always seeking experienced professionals with a GxP background to join our Consulting Division. Our Consulting Division specializes in guiding clients through the complex landscape of Good Manufacturing Practice (GMP) compliance, ensuring the highest standards of quality and regulatory adherence.

As a GxP Consultant, you will play a pivotal role in collaborating with diverse life sciences companies, leveraging your expertise to provide strategic guidance and support in navigating the regulatory environment.

Apply now, if you have a background in the following areas and want to be a part of a dynamic and innovative life sciences consulting firm dedicated to providing high-quality, compliant solutions to the pharmaceutical, biotechnology, and medical device industries.

  • Validation Services: Conduct and oversee validation activities for equipment, processes, and computer systems, ensuring compliance with industry standards and regulatory requirements.
    Quality Systems: Assist in the development and implementation of robust quality management systems, including documentation, training, and deviation management.
  • Regulatory Compliance: Collaborate with clients to ensure adherence to GxP regulations, providing expertise in Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Good Clinical Practice (GCP).
  • Risk Management: Utilize risk-based approaches to assess and mitigate compliance risks, fostering a culture of continuous improvement.
  • Client Collaboration: Work closely with cross-functional teams and client stakeholders to understand business needs, offering strategic insights and solutions.

Requirements

Qualifications:

  • Bachelor's Degree in engineering, science, or similar field or equivalent experience; Preferred Education: Masters's Degree in engineering, science, or similar field
  • Minimum of over 3+ years of experience in a GxP-regulated environment.
  • In-depth knowledge of FDA and international regulatory requirements.
  • Strong understanding of quality systems, validation processes, and risk management principles.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse teams.

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