Ireland Job Openings

Teva Pharmaceuticals

Analyst - QA

Waterford

October 15, 2024

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Analyst - QA
Date: Sep 13, 2024
Location:Waterford, Ireland, X91
Company: Teva Pharmaceuticals
Job Id: 58307
Who we are

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.
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 Assurance Analyst at our site in Waterford. This is a perm role.


The Quality Assurance Analyst is responsible for developing, maintaining and implementing quality standards and systems which give assurance that products comply with product licences, specifications and c GMP’s.
A Day in the Life of our Quality Assurance Analyst

  • To review batch documentation ensuring it is completed right first time and in full, in accordance with product licences, specifications and c GMPs.
  • To prepare, review and approve documents and reports to ensure compliance with regulatory guidelines.
  • To archive QA batch documentation.
  • To complete post QP batch related activities for customers.
  • To review, maintain and audit documents and processes in an efficient and timely manner in order to meet customer requirements both internal and external and ensure schedule adherence.
  • To act as a point of contact for external customers and to ensure all customers’ requirements are met in a timely manner.
  • To identify and make recommendations for improvements as part of a team within or outside the department in order to eliminate non value added activities and ensure continuous improvement.
  • To carry out audits to ensure that all operational processes are carried out in compliance with the required standards conforming to Company GMP, GLP, SOP, Specifications and Validation requirements.
  • To provide support for complaint investigation response and approval.
  • To track and support the CAPA system to maintain site compliance.
Who we are looking for

Are you….

  • Educated to Degree Level in a science related discipline and/or relevant experience in the healthcare industry

Do you have….

  • Knowledge of c GMP, regulatory bodies, customer requirements and environmental procedures.
  • Knowledge of Company policies, procedures and standards
  • Knowledge of production and Lab process and systems.
  • Knowledge of internal customers and suppliers.
  • Auditing skills.
  • Report writing experience
  • Documentation completion experience
  • Problem solving skills and process improvement experience
  • Teamwork/Collaboration Skills
  • Excellent planning and organisation skills
  • Good problem solving skills
Already Working @TEVA?
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
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.

Apply now »
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