As a global leader in generic medicines with a strong innovative portfolio, we are all in for better health.
Teva Pharmaceuticals has been developing and producing medicines for more than 120 years. Along with our established presence in generics, we have significant research and operations supporting our growing portfolio of innovative medicines and biopharmaceutical products.
Today, our portfolio of around 3,600 products is among the largest of any pharmaceutical company in the world. Nearly 200 million people in 60 countries benefit from one of Teva's quality medicines every day. We invest in research and development of innovative medicines, generic drugs and biosimilars, carrying on the legacy of more than a century of finding new ways to help patients improve their lives. This defines our values as a company and characterizes how we do business and approach medicine.
This defines how we do business and motivates thousands of Teva employees all over the world, every single day.
Learn more at .
In Bulgaria Teva (known as Actavis until 2020) is the largest employer in the pharmaceutical industry with near 1700 employees in the two manufacturing plants (Dupnitsa and Troyan), sales and marketing organization and in a number of global corporate functions based in our country. We believe that each and every one of us should have access to quality medicines that help manage illness, fight infection or simply support overall health. Learn more at .
We are excited to announce a new career opportunity for the Sofia office of Teva for the role of Artwork Quality Control Coordinator , part of the RA Artwork Management, Harlow department.
The Artwork Quality Control Coordinator will perform quality checks of new artworks, amends and final blueprint proofs in line with Regulatory and Business Unit requirements. Action daily tasks within Artwork Management system in line with departmental KPI and timelines. Work closely with other members of the department to resolve queries and deliver high quality artwork.
• Perform quality checks on every draft of artwork to ensure artworks are created in-line with studio brief. Compare the artwork content against the supplied text file to ensure artwork content is correct. Ensure artwork is built to the correct technical requirements, design guidelines and local regulatory requirements.
• Complete quality check of the final blueprint proof against the approved artwork.
• Have departmental sign off responsibilities for the approval of draft artworks and for the approval of the final blueprint proof for print.
• Ensure all approvals and quality checks are documented and logged in the relevant location.
• Provide clear instruction to Artworker for internal amends that fail QC checks.
• Work closely with Studio Coordination team to resolve queries and ensure ‘right first time’.
• Route approved artwork for approval to necessary stakeholders.
• Work efficiently to complete tasks in line with scheduled timeline of the Artwork Management System.
• Ability to recognise and prioritise key products. Working to expedited timelines to meet deadlines when required.
• Take corrective action when required. If necessary, escalate to Artwork or Coordination team.
• Ensure all processes, SOP and Working Instructions are adhered to thus minimising the occurrence of non-conforming materials.
• Ensure database and spreadsheets are updated in a timely manner.
• Adapt to continuous improvement within the department with the view of improving customer service and right first time.
• Attend team meetings for training updates as well as general communication.
• Relevant education
• Experience with proofreading or performing quality checks against Artwork briefs, technical requirements and design guidelines.
• Computer literate.
• Ability to work as part of a team and independently.
• Knowledge of packaging and/or the print industry desirable.
• Quality / Attention to detail.
• Fluent in English both written and spoken.
• Organised and methodical.
• Numerate and literate to a high standard.
• Clear communication.
• Problem solving and ability to work with team to resolve problems.
• Dynamic and challenging work environment in one of the world leading pharmaceutical company and the biggest pharmaceutical company in Bulgaria
• Competitive remuneration bound with performance
• Additional healthcare insurance
• Transportation allowance and additional flexible benefits
• Flexible working hours and option to work from home as per the company policy
• Opportunity for development
If this sounds like the right opportunity for you, send us your CV in English.
Please, kindly note that only shortlisted applicants will be contacted. All personal data is protected by law and will be treated in confidence.
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 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. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
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