Details

Contract

Full-Time

Location

Krakow, Poland

Department

Life Sciences

Openings

2

Job ID

50435279

MAKE HISTORY WITH US! Hi! We are Philip Morris in Poland and we are part of group Philip Morris International. While you’re reading this text, we are shaping smoke free future using technology. Brave enough to change the lives of millions of adult consumers around the globe? With huge change, comes huge opportunity. So, wherever you join us, you’ll enjoy the freedom to dream up and deliver better, brighter solutions and the space to move your career forward in endlessly different directions. JOIN US! WHO ARE WE LOOKING FOR? A person who is/has: • University degree in Science/Engineering or equivalent • Experience in qualification and validation of manufacturing processes and Computerized Systems • Fluent oral and written communication skills in Polish and English • Knowledge of ISO Management Systems • Experience in auditing of organization internally or externally against ISO 9001 • Strong soft skills: communication, negotiation, ability to coach, technology & business process acumen, deal with ambiguity, managerial courage, result oriented, project management • Good practical knowledge of MS Office (Excel, Word, etc.) WHAT WE OFFER YOU? • cross-functional projects • Cafeteria with various benefits • attractive medical care for you & family • a wide range of internal trainings • pension employee program • subsidized meals in company canteen HOW CAN YOU MAKE HISTORY WITH US? • Leading and executing validation activities that are identified and required (process, cleaning, CSV) and supporting all aspects of Computerized System Validation • Assuring that all computerized systems are validated in accordance with xGMP principles, regulatory requirements, and company policies and standards • Providing risk assessment for new computerized systems and changes to existing computerized systems • Executing and providing reviews of validation protocols and validation periodic monitoring • Managing the validation of new processes, computerized systems, as well as changes to existing processes and systems • Ensuring that all deviations during validation activities are investigated and escalated when required • Organizing and leading the Continued Verification Assessment and the re-execution of validation protocols according to the plan and procedures Please note that only on-line applications will be taken into consideration. Only selected candidates will be contacted

Apply