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Quality Officer

Date: Jun 8, 2021

Location: Waterford, IE, X91

Company: Teva Pharmaceuticals

Who Are We

 

We touch the lives of over 200 million patients every day, and billions every year. After all, everyone needs healthcare or medication at some point. Yet until today, you may not have heard of us.

We're Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world.

We would like to invite applications for the role of Quality Officer at our Waterford site.

The Quality officer will be responsible to ensure Teva Pharmaceutical Waterford business units are in compliance with regulatory requirements by timely review and release of batch documentation and conducting process, packing, cleaning and validation activities of all areas against the regulatory standards.

A day in the life of our Quality Officer

 

  • To ensure that all work carried out complies with the required standards conforming to company, cGMP, cGLP’s, SOP’s, regulatory regulations and guidelines, H&S and environmental guidelines.
  • Review and approval of change proposals and related documentation for compliance with regulatory requirements and GMP requirements. Manage document deliverables to ensure launch and submission targets/KPIs are met, while adhering to appropriate statues, regulations and guidance.
  • New Product/Validation: Quality support for introduction of new products, equipment and facilities. Partners with Engineering, R&D, Operations and other cross-functional partners to ensure the proper application of regulatory controls. To review validation activities in line with current regulations within required timelines.
  • Quality Systems Development: To develop and improve quality systems by identifying areas for improvement (NVAA’s and key variances) and take corrective action as required ensuring continuous improvement in accordance with Company Continuous Improvement Process.
  • To conduct simulated inspections to ensure the company is at all times in a complaint state.

Who we are looking for

 

Are you….

 

  • Educated to degree level preferably in a Science Discipline with experience in Pharmaceutical/Medical Device and a QA environment.

 

Do you have?

 

  • Experience in Validation Role would be an advantage.
  • Inhalations experience Would be an advantage.
  • In depth knowledge and understanding of interpretation of cGMPs and FDA and EU regulatory requirements.
  • Good knowledge of report writing, project management, continuous improvement and problem solving tools.
  • Computer System Validation experience.
  • Understanding of Production and Laboratory systems to effect decisions consistent with business needs.

Teva’s Equal Employment Opportunity Commitment

 

At Teva, we pride ourselves on being a company where we can all thrive, and where everyone feels comfortable being their true self.

Diversity and inclusion sits at the heart of everything we do. By valuing difference, we can be a better employer for our colleagues, and provide a better service for our customers and patients. That’s why we’re constantly looking for ways in which we can learn from each other, embrace what makes us unique and contribute to a fairer society free from discrimination and prejudice