Our story is one of leadership in global healthcare, with synergistic strengths and unique innovation.
We offer better healthcare and accessible Treatments to Millions Worldwide.
Building on our strong global footprint, size and scale, Teva is reaffirming its commitment to place people at the centre of our strategy.
Teva enables to live better, healthier days.
Working in an exciting global company such as Teva, increases your exposure to multiple areas, cultures, business and technologies.
Teva provides more opportunities to grow within!
Join us for a life changing adventure!
Introduction to Quality
Our dedication to quality in everything we do is uncompromising, and covers every stage of the development, production and marketing of our medicines: from the supply of materials through manufacturing and approval by the strictest authorities. Our state-of-the-art manufacturing facilities recognized by FDA approval of 26 of our plants, and EMA approval of 31 of our plants.
Are you an exceptional Scientist or Engineer looking to work with industry leaders, global markets and technologies that will light up your passion? Are you ready for our mission to become a global leader in generics and biopharmaceuticals, improving the lives of patients? Teva’s Global Quality should be your next station!
What You'll Be Doing
As a Quality Analyst, you will work effectively as part of a team and perform all compliance related activities for development projects in adherence with regulatory standards and Teva business objectives.
You will manage and execute Pharmaceutical Development Quality Assurance (PDQA) Project Plan activities.
You will observe and review development activities. To include manufacturing of development batches, testing of materials, process and methods validation and technology transfer activities
You will participate on project Chemistry, Manufacturing and Controls (CMC) teams as a PDQA representative.
You will liaise as required with external contractors performing development activities.
You will review and approve project related documentation to include, but not limited to, change controls, manufacturing protocols and records, specifications, certificates of analysis and stability tables.
You will ensure all out of specifications results and unplanned deviations are fully investigated and documented and any corrective and preventative actions are implemented.
You will review analytical validation activities so that these activities meet the required standards appropriate for the activity and phase of development.
What You'll Need
Degree in a Science based subject
Good understanding of the Pharmaceutical development process and associated ICH Guidelines
Knowledge of cGMP Quality Systems
Proven experience of working in a quality organisation with a focus on and understanding of development activities
Experience of pharmaceutical manufacturing and analytical procedures, processes and validation.
Good verbal and written communication skills. Ability to present effectively to groups and to get key points across.
What We Offer
25 days annual leave + public holidays
Private medical insurance
Employee Assistance Program
Excellent progression and development opportunities
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.