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Quality Manager / Auditor (m/f/x)

  • Location: Ingelheim am Rhein
  • Salary: negotiable per year
  • Job Type:Permanent

Posted 13 days ago

  • Sector: Pharmaceutical
  • Contact: Claudia Gines Madrid
  • Contact Email: c.gines@sciproglobal.de
  • Start Date: asap
  • Expiry Date: 02 September 2022
  • Job Ref: QA_2022_14_1659535807

Quality Manager / Auditor (m/f/x) | Pharma

In this role you will be primarily responsible for maintaining the Corporate Quality Management System on an international level. Together with the international QM team you are responsible for inspection preparation and execution. You support interdisciplinary projects in the QM area - group-wide as well as cross-company.

Your tasks as a „Quality Manager / Auditor (m/f/x)":

  • Contribute to the continuous improvement of the pharmaceutical quality system
  • Participate in mock audits and global self-inspections
  • Support in the preparation of inspections
  • Participate in cross-divisional, group-wide and / or cross-company projects

Details & Benefits:

  • Type of contract: unlimited
  • Salary: fixed salary + performance-related bonus, Christmas & vacation bonus, anniversary payments
  • Vacation: 30 days / year; special leave for certain occasions and to care for sick children
  • Working hours: 40 hours / week - flexible working hours model
  • Homeoffice: currently 100%

after COVID: home office policy with 2 fixed home office days / week

  • Training: Professional training on the job; technical, professional, and personal further training and promotion both internally and externally; development opportunities in the form of foreign assignments
  • Benefits: Company health management, company doctor with regular check-ups, health club including fitness trainers, various sports groups (yoga, soccer, cycling, etc.), cooperation with daycare centers, individual home office solutions if required, support in finding and moving to a new home, company apartments
  • Accessibility: Very good transport connections

Your profile:

  • Completed studies in Life Sciences
  • 3 years of practical experience in the pharmaceutical industry
  • Relevant experience in a GxP environment
  • Strong organizational and negotiation skills and efficient time management skills
  • High level of intercultural competence and a willingness to travel internationally (approx. 15%)
  • Business fluent in English, as you will be working predominantly in the English language

Information about our client:

Our client is an internationally operating pharmaceutical company that provides pharmaceutical services in the area of licensing, regulatory affairs and auditing as well as independently develops and offers active ingredients, their precursors and medicinal products. The company has an extensive portfolio of in-house developments and licensed products as well as subsidiaries e.g. in the USA, Japan and India. The company employs more than 150 people worldwide.