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Quality Analyst

Date: Jan 14, 2022

Location: Larne, GB, BT40 2SH

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 Analyst at our site in Larne.

The Quality Analyst is responsible for supporting Research and Development projects in Larne to ensure compliance to Teva and regulatory requirements and to meet overall business objectives.

A Day in the Life of our Quality Analyst

  • Ensure Quality Management system operates in compliance with Teva standards and regulatory requirements.
  • Review and approve project related documentation to include but not limited to deviations, change controls, laboratory investigations, manufacturing protocols and records, specifications, clinical trial documentation, clinical supply labels
  • Participate in internal audits as directed, including self, system, facility and line. 
  • External oversight of third party vendors (in conjunction with audit group) to support development CMC activities and regulatory requirements.
  • Perform Quality review of Larne site SOPs relating to IMPs, site qualification and operational activities
  • Participate and support regulatory inspections for Larne site.
  • Coordination and oversight of all QA activities for projects from development to technical transfer in cooperation with other functions internally as well as externally.
  • Participate on project teams, serve as QA project manager with project oversight and act as POC for all strategic project decisions, issues, discussions and ensures Quality by Design principles are applied and risk assessments are performed.
  • Provide quality review and approval for analytical validation activities so that these activities meet the required standards appropriate for the activity and phase of development.
  • Develop, implement and train on QA procedures as required and in compliance with Teva standards

Who we are looking for

Are you….

  • Educated to Degree Level in Chemistry or Pharmaceutical Sciences or closely related subject

Do you have….

  • Extensive experience in analytical or formulation pharmaceutical product development or Quality Assurance
  • Understanding of quality procedures related to formulation or analytical Pharmaceutical Development.
  • Knowledge of US and EU guidelines and implementation for CMC product development.
  • Experience auditing development CMC activities
  • Ability to work effectively in teams, foster teamwork and with other functional groups and meet the expectations of internal and external partners
  • Ability to present effectively to groups and to get key points across

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