Microbiologist I | |||||
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 | |||||
YOUR TASKS AND RESPONSIBILITIES
- 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.
- Support validation and implement testing of environmental monitoring samples, bioburden, monitoring and analysis (water, compressed air), endotoxin test, among others as needed.
- Responsible of support the development different kinds of documents as local SOPs and others.
- In charge of microbiology laboratory daily operations, possibility of regency.
- Responsible for the reliability of the daily analyses and results, data integrity, OOS and CAPA analysis, root cause investigation.
- Support to calibration and maintenance programs for the microbiology laboratory equipment.
- Laboratory metrics elaboration.
- Supports training of laboratory technicians (laboratory work).
- Able to track progress and escalate to Microbiology Supervisor, if needed.
- Able to substitute for the supervisor in case of absence.
- Capable of laboratory team management.
- Responsible for compliance with GLP, biosafety guidelines, HSE guidelines, internal procedures and others related.
- Support procurement process and inventory management.
- Any other activities can be delegated once training is completed.
WHO YOU ARE
- Licentiate degree in Microbiology or Biotechnology (Mandatory).
- At least 1 year of experience in microbiological laboratories.
- At least 1 year of experience in industrial test or test validations is preferred.
- Advanced English proficiency.
- Able to documents creation, Validation Protocols and others related activities.
- Knowledge in validation of analytical methods.
- Knowledge of QMS systems and subsystems.
- Process Validation Knowledge.
- Knowledge of laboratory systems and systems management.
- Knowledge of environmental monitoring sampling and test included but no 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.
- Ability to build relationships and partnerships within the organization.
WHAT WE OFFER YOU
- Competitive salary.
- Attractive benefits package.
- Wide range of development opportunities.
- 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's unique capabilities, self-experiences, and aspirations. We, intentionally seek diversity, to enable our people to 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 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, or gender identity and will not be at a disadvantage if unemployed.
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Application Period: | 12/26/2024 - 01/08/2025 | Reference Code: | 836420 | |
Division: | Pharmaceuticals | Location: | Alajuela, Costa Rica | |
Functional Area: | Quality | Work Time: | Full time | |
Employment Type: | Regular |
Contact Us | |||
Address | |||
Coyol de Alajuela, Costa Rica | |||
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