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Microbiologist II 

 
   

Ever feel burnt out by bureaucracy? Us too. That’s why we’re changing the way we work for higher productivity, faster innovation, and better results. We call it Dynamic Shared Ownership (DSO). Learn more about what DSO will mean for you in your new role here https://www.bayer.com/en/strategy/strategy

 

 

TASKS AND RESPONSIBILITIES
 

  • In charge of microbiology laboratory daily operations.
  • Lead and support the developing, transferring and implementation of testing methods for starting materials, device components, packaging materials and drug products according to approved and validated test methods.
  • Responsible of leading and supporting the development of different kinds of documents as local SOPs among others.
  • Responsible for the reliability of the daily analyses and results, data integrity, OOS and CAPA analysis, root cause investigation.
  • Any other duty upon completion of the corresponding training.

 

WHO YOU ARE
 

  • Graduated Microbiologist, incorporated in the CMQC Professional Association (Colegio de Microbiólogos de Costa Rica) is Mandatory.
  • At least 1 year of experience in Medical Devices or Pharmaceutical Industries is Mandatory.
  • Advanced or native English and Spanish languages, both written and spoken.
  • Knowledge in validation of analytical methods, QMS systems and subsystems.
  • Process Validation Knowledge.
  • Knowledge of environmental monitoring sampling and test included but not limited to water, air, surfaces and others.
  • Knowledge of critical systems monitoring, included but not limited to endotoxin test, sterility test and others related.
  • Knowledge of pharmaceutical and medical devices culture methods.
  • Knowledge of microbiological identification methods.
  • Proficient with Microsoft Office tools.
  • Demonstrated advanced problem-solving abilities.
  • Knowledge of current Good Manufacturing Practices (cGMP s).
  • Knowledge of ISO system (9001, 13485, 14644, 17025) is desirable.
  • Demonstrated ability to communicate verbally and in writing at a level commensurate with regulatory and technical reporting requirements.
  • Ability to multitask in a fast-paced work environment and to self-direct, as required.
  • Ability to manage technical information and reports.
  • Ability to be flexible in changing daily workload priorities as directed.
  • Ability to work in a team environment, to build relationships and partnerships within the organization.

 

WHAT WE OFFER YOU

 

  • Full time employment contract
  • Wide range of development opportunities
  • Competitive salary
  • Attractive benefits package
  • Good working conditions and comfortable working environment
 

At Bayer we believe in diversity, equity, and inclusion. We aim to create an environment in which everybody can feel authentic, respected, and equally valued. Every day we strive to reflect our values through our people unique capabilities, self-experiences, and aspirations. We, intentionally seek diversity, to enable our people bring their fullest potential out and encourage others to likewise do so. Our company wins, when we leverage our capabilities to lead the cultural transformation in our business, positively impacting the society.
 
Candidates who meet the requirements based on the job profile will be considered for employment regardless of physical disability, race, color, religion, sex, age, sexual orientation, gender identity and will not be at a disadvantage if unemployed.

   
Application Period: 05/09/2025 - 05/22/2025 Reference Code: 845592    
Division: Pharmaceuticals   Location: Costa Rica : Heredia : Heredia    
Functional Area: Quality   Work Time: Full time  
Employment Type: Regular       
 
 
Contact Us
 
Address   E-Mail
Alajuela, Costa Rica

 

HROP_TA_PACA@BAYER.COM 

 

 

 
 
 


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