Director of Quality Assurance - Frankfurt am Main, Deutschland - Vida Group International

Vida Group International
Vida Group International
Geprüftes Unternehmen
Frankfurt am Main, Deutschland

vor 2 Wochen

Lena Wagner

Geschrieben von:

Lena Wagner

beBee Recruiter


Beschreibung

Our client, a leader in medical device and pharmaceutical manufacturing, is seeking a Director of Quality Assurance for their Frankfurt location.

This is a newly created position and will oversee GCP and R&D.


Responsibilities:


  • Ensure compliance for R&D and all Global clinical studies
  • Support clinical study teams throughout course of trial by developing study
- specific Quality Audit Plans to support audit conduct through study lifecycle

  • Attend clinical study meetings to provide consistent Quality oversight
  • Responsible for performance management, training, and task oversight
  • Identify and escalate compliance risks or issues
  • Utilize Global R&D Quality Management System in support of daily operations and audit management
  • Manage global audits and inspections
  • Conduct audits within multiple GCP areas, including but not limited to: Investigator site, vendor, documentation, eTMF for both drug and device clinical trials
  • Perform audit management tasks in accordance with expected procedural timeframes
  • Provide support as needed for potential procedural updates
  • Identify and implement process changes within the R&D processes to support continual process improvement
  • Facilitate and support harmonization initiatives within the R&D group
  • Facilitate and support projects to improve R&D compliance and operational efficiencies
  • Ensure applicability of current quality policies, procedures, and objectives by staying informed of the latest updates/modifications related to applicable regulations (ISO, Ministries of Health (FDA, EMA, Health Canada, TGA, ANVISA, etc.)
  • Provide updates to R&D staff as applicable

Qualifications:

  • Bachelor's degree required
  • Master's degree preferred
  • 15+ years experience in Clinical Quality/Compliance
  • 7+ years Audit experience
  • 5+ years experience in Medical Device Clinical Trials or Biologic Clinical Trials
  • 5+ years staff management experience
  • Strong knowledge of US and EU/International GxP (GCP, GLP, GDP) and medical device regulations and guidance
  • Strong verbal and written communication skills

Pay:
,00€ ,00€ per year


Ability to Relocate:

  • Frankfurt: Relocate before starting work (required)

Work Location:
In person

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