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Teva Pharmaceuticals Quality Officer - 6 Month FTC in Waterford, Ireland

Quality Officer - 6 Month FTC

Date: Oct 15, 2020

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 are looking for a Quality Officer to join the team at our Waterford site for a 6 month Fixed Term Contract.

The Quality officer will be responsible to ensure Teva Pharmaceutical Waterford R&D 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….

  • You will ensure that all work carried out is in Compliance with the required standards conforming to company, cGMP, cGLP’s, SOP’s, regulatory regulations and guidelines, H&S and environmental guidelines.

  • You will review and approve change proposals and related documentation for compliance with regulatory approvals and GMP requirements. Review and assistance in Laboratory, Complaint, Vendor and Manufacturing investigations and reduction of trends in conjunction with relevant departments.

  • You will be involved in new Product Introduction and Technical Transfers: Quality support for introduction of new products, equipment and facilities. Partners with Operations and other cross functional partners to ensure the proper application of design controls and risk management.

  • You will review and prepare manufacturing and packing records, and product Specification files for Clinical release: Conduct documentation review of batch records in line with regulatory requirements, including where applicable, Deviation, OOS and Stability investigation reports.

  • Quality Systems Development: You will 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.

Who we are looking for

Are you….

  • Able to participate in day to day activities and projects by providing Quality support?

  • Able to work on your own initiative to meet and exceed business objectives?

  • Able to understand internal / external customer requirements and can respond promptly to their needs?

Do you have….

  • A Qualification in a Science discipline and experience working in a Pharmaceutical / Medical Device company with experience in a QA environment?

  • In depth knowledge and understanding of interpretation of cGMPs and regulatory requirements, experience of regulatory inspections and customer audits?

  • Understanding of Production and Laboratory systems to effect decisions consistent with business needs?

  • Experience with Trackwise, SAP and strong report writing skills?

  • Computer System Validation experience? (Preferably)

  • Experience of combination product / medical devices/pharmaceuticals manufacturing? (Preferably)



Sub Function

Quality Assurance Methods

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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.

EOE including disability/veteran