Coordinator Deviation / CAPA (m/w/d) New Assets

TN Germany; Frankfurt; Hybrid; EUR 55.000 - 70.000; Vollzeit

Zusammenfassung

A leading company in the pharmaceutical sector seeks a Deviation/CAPA Coordinator to join their global quality operations team. The role involves managing deviations and CAPAs, ensuring compliance with quality standards, and supporting QA processes. Ideal candidates will have a background in science or engineering, with substantial experience in quality assurance. The company offers a hybrid work model, competitive remuneration, and opportunities for career development.

Leistungen

Opportunities for career development

Hybrid work model

Modern workplaces

Global company culture

Competitive remuneration

Employer-subsidized benefits

Qualifikationen

• 5+ years experience in deviation/CAPA management.
• 3-5 years in a pharmaceutical environment, especially in QA.

Aufgaben

• Co-design process definitions for deviations and CAPAs.
• Organize, execute, and document deviation and CAPA systems.
• Act as contact for JIRA modules and provide training.

Kenntnisse

Analytical Thinking

Communication

Team-oriented

Ausbildung

Scientific Studies in Science or Engineering

PTA Education

Tools

Microsoft Office

Jobbeschreibung

The provided job description contains useful information but requires improvements in formatting, clarity, and removal of irrelevant or redundant content. Here is an improved version:

Job Title: Coordinator Deviation / CAPA (m/w/d) New Assets

Location: Frankfurt, Germany

Job Category: Other

EU Work Permit Required: Yes

Job Reference: 1683ffe4d38e

Job Views: 1

Posted: 16.05.2025

Expiry Date: 30.06.2025

Job Description

Join our global quality operations team as a Deviation/CAPA Coordinator in Quality. Your responsibilities will include:

• Co-designing process definitions for deviations and CAPAs, including creation and updating of department-specific SOPs
• Organizing, executing, and documenting the deviation and CAPA systems, monitoring deviations and CAPAs, and supporting QA in their processing
• Acting as the contact person for relevant JIRA modules, providing training sessions on deviation and CAPA systems
• Handling non-conformities and CAPA issues for internal and external customers
• Creating data to track due dates of quality-relevant JIRA modules

Your Profile

• Completed scientific studies in Science, Engineering, or a similar field, or alternative education as PTA with over 5 years of experience in deviation/CAPA management
• 3-5 years of professional experience in a pharmaceutical environment, particularly in quality assurance
• Proficiency in Microsoft Office, database queries, and basic statistics knowledge
• Knowledge of national and international pharmaceutical and medical device requirements
• Strong analytical thinking and ability to present complex matters clearly
• Team-oriented, proactive, and well-organized
• Perseverant, independent, and self-motivated work style
• Excellent communication skills in German and English

Benefits

• Opportunities for individual career development and making a positive impact on patients' lives
• Hybrid work model supporting work-life balance
• Modern workplaces with good transport links and a company restaurant
• Global company culture with flat hierarchies and respectful environment
• Competitive remuneration and social benefits
• Employer-subsidized benefits such as WellPass, Deutschland-Ticket, Corporate Benefits, and JobBike

Find out more about our benefits here.