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 Responsabilities
- Responsible of the Microbiological Regency according to CR regulation.
- Responsible of technical reports and support areas as a SME in microbiology.
- Validate/Verify and implementation of testing methods for starting materials, device components, packaging materials and drug products.
- Responsible for the reliability of the daily analyses and results, data integrity, OOL, OOS and CAPA analysis, root cause investigation.
- Able to track progress and escalate to Lab Supervisor.
- Responsible for compliance with GLP, biosafety guidelines, HSE guidelines, internal procedures and other related.
- Any other activities can be delegated.
Who You Are
- Required graduated in Microbiology or Biotechnology.
- 1 years of experience in medical devices/pharmaceutical microbiological laboratories.
- 1 years of experience in industrial test or test validations is preferred.
- Advanced English reading, writing and speaking skills.
- REQUIRED KNOWLEDGE:
- Knowledge in validation of analytical methods.
- Knowledge of QMS systems and subsystems.
- Process Validation Knowledge.
- Knowledge of laboratory systems / systems management.
- Knowledge of critical systems monitoring, included but not limited to endotoxin test, sterility test and others related.
- Knowledge of pharmaceutical / 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).
- Ability to self-organized and prioritized task.
- Ability to multitask in a fast-paced work environment.
- 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.
- Ability to problem solving mindset.
- Ability 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: 8/28/2025 - 11/09/2025 Reference Code: 852577
Division: Pharmaceuticals Location: Costa Rica : Heredia : Heredia
Functional Area: Quality
Employment Type: Regular Work Time: Full-Time
Contact Us
Address
Coyol, Alajuela, Costa Rica
