**Quality Specialist AP**When you show proactivity and ambition, we'll harness it through a variety of opportunities and challenges in the diverse areas of our business - all with a strong and meaningful purpose. Where do you want to go? What do you want to do? How do you want to make a difference? The choice is yours, and we'll help you get there**. Be better together. Be Bayer.****YOUR TASKS AND RESPONSIBILITIES**- Main Quality responsible with production and engineering to ensure entire operational readiness for the manufacturing process and adequate technology transfer process.- Work with the production and engineering departments creating, reviewing and approving product related procedures.- Certification and Batch release of the production and packaging batches.- Ensures that products are manufactured and tested according to valid methods and batches meet specifications prior to release. Coordination and approval of deviation investigations related to the product.- GMP support to production department including GMP Continuing Training Program- Responsible to hire, train, guide and lead quality inspectors and trainers.- Provide appropriate initial and continuing training for the quality inspectors and trainers.- Any other duties can be delegated once training is provided, if required.**WHO YOU ARE**- Licenciate Degree in Pharmaceuticals (need to belong to the Colegio de Farmacéuticos de Costa Rica).- Advanced writing and speaking English level in order to understand, interpret, do and communicate fluidly general instructions and techniques in English to Spanish- 3 years of experience in production or quality assurance departments in the Pharmaceutical or Medical Device Industry.- Knowledge of EU GMP, national and international pharmaceutical regulations are required (FDA, EU GMP, RTCA 11.03.42.07). Demonstrated advanced problem-solving abilities.- Ability to multi-task in a fast-paced work environment and to self-direct, as required.- Ability to be flexible in changing daily workload priorities as directed. Ability to work in a team environment.**Application Period**:- 29/04/2024 - 06/05/2024**Reference Code**:- 816352**Division**:- Pharmaceuticals**Location**:- Costa Rica : Heredia : Heredia**Functional Area**:- Quality**Work Time**:- Full Time**Employment Type**:- Regular**Work Time**:- Full Time**Contact Us****Address****E-Mail**- Alajuela, Costa Rica
