Sr Microbiologist

at  Abbott Laboratories

Alajuela, Provincia de Alajuela, Costa Rica -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate07 Sep, 2024Not Specified07 Jun, 20243 year(s) or aboveMedical Devices,Steam,Environmental Monitoring,English,Microbiology,Pharmaceutical Industry,Working ExperienceNoNo
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Description:

ABOUT ABBOTT SR MICROBIOLOGIST

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.

REQUIRED QUALIFICATIONS

  • Bachelor’s in microbiology or related field.
  • 3-5 years of working experience in a medical device / pharmaceutical or related industry in microbiology and /or sterilization roles.
  • Experience in environmental monitoring, process and product monitoring in a medical devices or pharmaceutical industry.
  • Experience in sterilization validation for Ethylene Oxide, Steam or Chemical sterilization processes.
  • Proficiency in computer applications (MS Excel, MS Word, MS PowerPoint).
  • Articulates microbiology technical concepts well.
  • Advance Commands of English required.
  • Available to work 100% on site (Coyol, Alajuela).
  • Shift Administrative (Monday to Friday 8:00 am -5:00 pm).

PREFERRED QUALIFICATIONS

  • Experience working in a cross-division business unit model, preferred.
  • Master´s degree in microbiology, science, administration or retaled.
  • Supervising experience.

Responsibilities:

  • Provides Facility Microbiological Support
  • Record review of routine microbiological test results
  • Routine release of manufactured product
  • Technical support for facility issues in the areas of sterilization, environmental monitoring, and microbiological methods.
  • Handles routine out of specification test results, or more complex out of specification issues.
  • Data analysis of sterilization processes.
  • Participate in audits of sterilization, test lab, and biological product vendors.
  • Documentation
  • Ensures correct documentation linkage flow for microbiologically related documents.
  • Writes new or updates current microbiologically related documents.
  • Maintains understanding of applicable standards and applies them to qualifications and test methods.
  • Writes appropriate validation protocols; performs or oversees validations for new technologies, equipment, and/or test methods; creates documentation for implementation.
  • Develops sterilization cycles and laboratory test methods.
  • Works with technicians in conducting these qualifications.
  • Technical training
  • Provides training to laboratory technicians on new equipment or new test procedures.
  • Provides training in the areas of sterilization validation and sterilization processes.
  • Authority to sign off Qualifications, DDAs, NCMRs, COs, FMEAs, PDP forms.
  • Member of R&D product teams, Operations project teams, or supports other projects as Directed by Department Manager.
  • Occasional supervising of technical employees at the laboratory may apply to the role.


REQUIREMENT SUMMARY

Min:3.0Max:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Administration

Proficient

1

Alajuela, Provincia de Alajuela, Costa Rica