Cleaning And Validation Specialist - Sterile Product

Cleaning And Validation Specialist - Sterile Product
Empresa:

Teva Pharmaceutical Industries Ltd.


Lugar:

Álava


Área:

Otros

Cleaning And Validation Specialist - Sterile Product

Detalles de la oferta

Cleaning and validation specialist - Sterile Product Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth! Job Purpose Responsible for the site cleaning validation program and visual inspection validation. Main activities and responsibilities Responsible for the entire extent of cleaning validation concerning the plant production facilities and the maintenance of the qualification status in compliance with the VMP Organizes the activities related to cleaning validation interacting with production and other departments Assesses the impact of new substances on the existing process, determines the residual limits on which analytical methods and validation plans are developed and which are subject to inspection Evaluates the toxicological relationships necessary to develop cleaning protocols Defines the criteria for setting up validation plans and validating analytical equipment, and developing its protocols Defines the criteria for production equipment validation plans and, by developing its protocols Responsible for the validation of recipes set up on the automatic visual inspection for new products and the final issue of the validation report Owner of validation reports Responsible for VMP the cleaning qualification status of the manufacturing equipment in the annual review and updates Subject matter expert for the introduction of new products / processes Subject matter expert in the sterile sites TGO network Authors of risk assessments for cleaning topics including cross contamination Minimum Experience / Training required Master degree in CTF; biotechnology or equivalent At least 5 years of experience in sterile manufacturing pharma industry Consolidated experience in sterile production, particularly in aseptic process areas Fluent in Italian and English Good ability to work in teams Good autonomy and ability to organize work in accordance with the defined timelines Good capacity of problem solving Ability to work in a dynamic environment Analytical, decision-making capability and problem solving skills We offer The company offers a chance to work in a vibrant international environment that encourages out of box thinking and the development of new ways of doing things, whilst promoting professionalism and the chance to continue your professional development. 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.


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