MS&T Director

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

Join our dynamic team in Krakow as a MS&T Director, where innovation meets expertise. Be at the forefront of pharmaceutical technology, driving excellence and shaping the future of our Manufacturing Science and Technology department. 

How you’ll spend your day

• Management and responsibility for each team within the department. Close collaboration with the site’s stakeholders (Manufacturing, Engineering, Quality…).
• Making the necessary decisions in all matters concerning the department to ensure its proper functioning.
• Ensuring the continuity of the production process, based on the technology and resources including the appropriate efficiency, costs and management of production and technology processes.
• Supervision of technological processes:

- Technology transfer,
- API&Excipients changes,
- Changes in manufacturing equipment, packaging lines,
- optimization of technology,
- Technological documentation preparation,
- Preparation of cleaning plans and hygiene procedures,
- Validation Master Plan preparation,
- Process and cleaning validation,
- Preparation of qualification schedules and qualification reports,
- Equipment and system qualification,
- Environmental monitoring - annual trends.

• Coordinating the high-efficiency projects and active participation in individual projects (LEAN, OEE, 5S, SMED, VSM).
• Product Robustness and continuous improvement.
• Implementation of local and corporate guidelines, standards concerning the production area (production & technology).
• Coordination of investment projects, investment budget control, supervising investment processes in accordance with corporate guidelines.
• Collaboration with the Quality Division in terms of continuous monitoring and improvement of Quality system.
• Identifying talents in organization, employee performance and succession plans management. Developing employees, being their mentor, modeling behaviors and competencies in line with the Teva’s values.
• Planning and budget management. Establishing priorities in the Division’s budget. Workload and resources administration/ disposal.
• Collaboration with the Environmental Protection Department in terms of identifying ways and methods of disposal of waste generated in the plant, sewage neutralization, reduction of gas, dust and noise emission into the air.

Your experience and qualifications

• MSc. in Science, Pharmacy or Chemical Engineering, Pharmaceutical Technology or equivalent experience. Ph.D. desirable.
• Minimum of 10 year experience in manufacturing. Additional specialist experience (e.g., pharmaceutical formulation, process development, manufacturing technology, aseptic techniques, regulatory processes).
• Leadership skills.
• Proactive and creative, solution oriented.
• Fluent in English.
• Knowledge of Microsoft Office. SAP, TrackWise desirable.
• Proven experience with Lean OpEx methodology.
   

Enjoy a more rewarding choice

• Annual bonus
• Christmas and New Year bonus 
• PZU group insurance 
• PZU Pogodna Jesień - retirement insurance
• Luxmed 
• Benefits from the Social Fund (Cafeteria, Multisport, etc.)
• Fruits on Tuesdays
• Co-financing for meals

Make a difference with Teva Pharmaceuticals

Apply online today!

Pre-employment verification

All job offers at Teva Poland are preceded by pre-screening candidates. In the case of all candidates who have passed to the final stage of recruitment, verification of the data provided in the recruitment process will be carried out, if deemed necessary. More detailed information will be provided to candidates prior to the verification process.

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. 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.