Quality Assurance Officer

Company Info

Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

What you will be doing

To develop, implement and maintain quality standards and systems to ensure that products comply with Marketing Authorisations, specifications and cGMP

• To support manufacturing and other operations in the development, implementation and maintenance of cGMP standards
• To review and approve batch manufacturing and packaging documentation within agreed timelines to support product release spending at least 50% of time on line performing batch reviews and line audits.
• To review and approve quality documentation to ensure compliance with cGMP and RFT
• To prepare and complete product quality reviews to ensure compliance with regulatory requirements Product Quality Review OTIF RFT
• To close out failure investigations and preventative actions to reduce repeat failures and to monitor actions to prevent overdue actions
• To identify, design and deliver cGMP training to support improved application of cGMP standards
• To carry out audits to support the identification, auctioning and close out of non-compliance issues Audit schedule and Audit actions

What you will need: Your profile

• Degree qualified in a science discipline
• Experience in a pharmaceutical industry in similar role
• Sterile Manufacturing experience essential
• Understanding of EU & US guidelines and the product licensing processes
• Understanding of GMP requirements in relation to sterile product manufacture and packaging
• Understanding of Lean manufacturing techniques
• Understanding of Quality Management Systems
• I.T. Literate
• Auditing/Problem solving
• Coaching skills
• Results driven
• Attention to detail

What we offer

• 20 days paid holiday per year - with the option to buy and sell up to 5 days annual leave each year
• The flexibility to work shift (days and nights)
• Company pension – flexible employee contributions
• Competitive salary
• Employee assistance programme
• A number of health benefits including: Life Assurance, Critical Illness Insurance, Income protection
• Plus many other flexible benefits via salary sacrifice: Cycle to work scheme, online and in store discounts and much more

Function

Sub Function

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

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva’s global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

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