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Expert Principal MS&T

Date: Jun 24, 2024

Location:

Dupnitsa, Bulgaria, 2600

Company: Teva Pharmaceuticals

Job Id: 56578

Who we are

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 www.tevapharm.com.

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 www.teva.bg.

We are searching for qualified and motivated candidate for the role of Expert Principal MS&T , based in Dupnitsa .

The opportunity

The main purpose of this role is to implement the strategy and to determine the methodology of for the validation of the production processes.

How you’ll spend your day

• Create the process validation strategies in accordance with the requirements of the company's policy for validation and maintenance of the validation status

• Participate in validation activities, by implementing harmonized corporate methods and validation documents, in order to achieve compliance with all GMP requirements of the regulatory agencies for which Dupnitsa is approved and certified for the export of medicinal products

• Execute tasks based on the corporate policies and on the basic and the standard operating procedures for validation

• Prepare or participate in the preparation and verification of the SOPs and the formats related to process validation activities

• Create the monitoring strategies

• Prepare risk assessment to determine the number of batches needed for the process validation

• Perform statistical analysis to assess the sustainability of the processes

• Participate in planned and unplanned inspections and customer audits

• Work on the material change

• Participate in activities related to Quality Improvement Programs (Product and Process Review) and other

Your experience and qualifications

• University degree preferably in Pharmacy, Chemistry or Biology

• Minimum of 3 years of experience in a pharmaceutical manufacturing and/or control of medicines environment

• Very good computer skills - MS Office

• Very good command in English language - written and verbal

• Proven skills in using statistical programs and/or performing statistical analyses

• Good understanding about the Law on Medicinal Products in Human Medicine, the regulatory requirements for the production of medicines in Bulgaria, the European and other international standards for Good Manufacturing Practice (GMP)

• Professional attitude and service orientation, to be a good team player

• Excellent time management skills

Enjoy a more rewarding choice

• 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

• Additional benefits according to the company policy

• Opportunity for future career development

Make a difference with Teva Pharmaceuticals

If this sounds like the right opportunity for you, send us your CV in English.

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 (https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte_company=1080030P)

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. 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.

EOE including disability/veteran