Quality Analyst

at  AbbVie

Company Description
AbbVie’s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.
Job Description

QUALIFICATIONS

• A third level qualification in a scientific discipline, preferably a B.Sc./M.Sc.
• At least two years pharmaceutical experience with good working knowledge of cGMP.
• Strong knowledge of FDA/EMEA regulatory requirements.
• Excellent organisational, communication and interpersonal skills.
• Ability to set and maintain the highest standards.
• Available for shift work as required
  Additional Information
  AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status

• Carries out QA inspection of starting and packaging materials, in-process and finished materials.
• Carries out sampling of starting and packaging materials, inprocess and finished materials.
• Performs room release and batch sign in for manufacturing operations
• Carries out and monitor established QA/GMP programmes.
• Carries of Environmental Monitoring and trending
• Gives assistance in the retain system for samples and documents.
• Carries out Batch Manufacturing Review and review of batch related documents.
• Provides assistance in departmental and regulatory audits.
• Has the ability to train a colleague in a particular GMP procedure or related activity.