Quality Assurance Specialist

vor 2 Wochen

Hamburg, Hamburg, Deutschland SciPro Vollzeit

Job Title: QA Manager

Job Overview:

In this role, you will be responsible for ensuring the quality of our pharmaceutical products by implementing and maintaining quality assurance processes. This includes supporting batch documentation review, participating in internal audits, and handling deviations and non-conformances. You will also be responsible for maintaining accurate QA documentation and ensuring compliance with regulatory requirements.

Key Responsibilities:

  • Implement and maintain quality assurance processes for pharmaceutical manufacturing.
  • Support batch documentation review to ensure compliance with GMP guidelines.
  • Participate in internal audits and prepare audit reports to identify potential quality issues.
  • Handle deviations, non-conformances, and CAPAs.
  • Maintain accurate QA documentation and ensure compliance with regulatory requirements.
  • Support product inspections and sampling to ensure quality standards are met.
  • Collaborate with production, R&D, and regulatory teams to address quality-related issues.
  • Participate in training programs related to QA and regulatory standards.

Qualifications:

  • Bachelor's degree in pharmacy, chemistry, biology, or a related scientific field.
  • Knowledge of GMP regulations and quality standards in the pharmaceutical industry.
  • Strong attention to detail and excellent organizational skills.
  • Good communication skills, both written and verbal, in German and English.
  • Ability to work in a team environment and contribute to cross-functional teams.
  • Basic computer skills, including proficiency with MS Office.
  • Strong interest in quality assurance and regulatory compliance in the pharmaceutical industry.

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