Qualified Person

Discover International; Nordrhein-Westfalen; Hybrid; EUR 65,000 - 85,000; Full time

Benefits offered by this job

Flexible hybrid working model

Clear progression path

Friendly and open company culture

Competitive salary package

Job summary

A leading biopharmaceutical company in Germany is seeking a Recruitment Manager for their Quality department. The ideal candidate will oversee Batch Release for Biological products and collaborate with multiple departments. Candidates must have at least 5 years of Pharmaceutical QA GMP experience. This role offers a flexible hybrid working model and a competitive salary package.

Qualifications

• 5+ years' experience in Pharmaceutical QA GMP.
• Flexible critical thinker.
• Ability to manage cross-functional teams.

Responsibilities

• Oversee Batch Release and relevant documentation for Biologics.
• Compile Quality Reports and document findings.
• Support Internal and External Audits.

Skills

Pharmaceutical QA GMP experience

Knowledge of QA Processes

Organizational skills

Job description

1 day ago Be among the first 25 applicants

Direct message the job poster from Discover International

Recruitment Manager Quality Europe at Discover International

We are partnered with one of Germany's most exciting, and innovative Biopharmaceutical companies, who are currently going through a phase of growth. They are expanding their Quality department for their HQ site in Hesse, and are seeking a Qualified Person to release their Biological products and generally contribute to the strategic direction of the Quality department.

The ideal candidate is a critical thinker that is flexible and can manage working across multiple areas. As a Qualified Person you should bring experience in evaluating processes within the Quality Systems of change management, deviation and CAPA management, and experienced in overseeing Batch release and relevant documentation. With a focus on Vaccines, Blood products, and mAbs, this company offers a unique opportunity to join a fast growing organisation and help make a positive change with the world of medicine.

Responsibilities

• Batch Release and relevant Documentation for Biologics pipeline.
• Work cross-functionally across multiple relevant departments.
• Compile Quality Reports and document findings.
• Qualifying and Managing external Vendors.
• Perform Root Cause and Risk analysis.
• Support Internal and External Audits.

Requirements

• 5+ years' Pharmaceutical QA GMP experience.
• Clear knowledge of QA Processes.
• Highly organized.

Package

• Flexible hybrid working model
• Clear progression Path.
• Friendly and open company culture
• Competitive salary package

Reach out via [e-mail] for more details.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance and Manufacturing

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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