Quality Analyst (12 Month FTC) Larne, Northern Ireland
Job description
Quality Analyst (12 Month FTC)
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. 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, analytical methods, specifications, manufacturing protocols and records, clinical trial documentation, clinical supply labels.
- Perform Quality review of Larne site SOPs relating to IMPs, site qualification and operational activities.
- Participate in internal audits as directed, including self, system, facility and line.
- 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.
- Develop, implement and train on QA procedures as required and in compliance with Teva standards.
- Preform trending, collect and review KPI data and assist Management in developing and implementing any necessary actions plans and/or CAPAs.
Who we are looking for:
Are you….
• Educated to Degree Level in Chemistry or Pharmaceutical Sciences or closely related subject.
Do you have….
• Experience of working in a Quality Assurance, Compliance or Quality Control role in support of GMP laboratory, manufacturing or pharmaceutical development operations.
- Excellent understanding of GMP.
- Experience of drafting and reviewing quality documentation, e.g., analytical methods, specifications, manufacturing documentation, validation protocols, technical reports.
- Experience of conducting and reviewing deviation and laboratory investigations.
- Experience of managing change controls and CAPAs.
- Experience of auditing or self-inspections.
- Experience of conducting training.
- Ability to work effectively in teams, foster teamwork and with other functional groups and meet the expectations of internal and external partners.
- Excellent attention to detail.
- Ability to present effectively to groups and to communicate key points.
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
