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Expert Microbiologist

  • Test Triangle Software Services
  • Job Type : Permanent

  • room Ireland /Tipperary North Riding

Number Of Applications : 1

Job Posted On : 25/10/2023

Job Posted On : 25/10/2023

  • Onsite

    Yes

  • Remote Work

    No

  • Experience Required

    8 - 14 yrs

  • Start Date

    Nov 5, 2023

  • Number of Positions:

    1

  • Visa Sponsorship

    No

  • Spoken Languages

    English

  • Job Post Currency

    Negotiable

REQUIRED SKILLS

OSD-Antibiotic Plant
Pharma
Microbiologist
PERMANENT
Annual Salary: Negotiable

Job Description

 Job Description:  

Please find the below job description for a microbiologist role. 

  • Preparing Validation Protocols and executing Product Validation activities related to Microbiology. 
  • Preparation and review of SOPs, GTPs, STPs, IOCPs, Miscellaneous study protocols and reports. 
  • Responsible for Microbial Testing and Review of Water, RM, Packing Material, In-process, Finished Product, and Stability samples. 
  • Microbial limit testing and method validations of Raw materials, Hold time samples, Finish products, and Stability samples. 
  • Production and Microbiology area environment monitoring (Active and Passive Air Sampling, Surface Monitoring) of Oral Solid Dosages Manufacturing. 
  • Microbial analysis (TAMC and Pathogen Testing) of water samples (Purified/ WFI/ Pure Steam/ Raw/ Potable Water). 
  • In-process, finished product, and Packing material Bioburden test performed. 
  • Bacterial Endotoxin Testing and Method Validation. 
  • Media Preparation, Sterilization, and Growth Promotion. 
  • Laboratory equipment/ instruments Calibration. 
  • Responsible for investigating excursion results during environmental monitoring and water Analysis. 
  • Review of Equipment, Instrument, Utility Systems Qualification, and Verification of electronic data generated at the laboratory during testing and software. 
  • Review Audit trail of Equipment, Instrument, and systems software. 
  • Thorough understanding of USP/NF, EP, and BP testing 
  • Handling of QMS activities like Change Control, Events, Deviation, Investigation and CAPA. 
  • Review Good Laboratory Practices to Ensure GMP Compliance, Laboratory Compliances, and inspection readiness at Site. 

  

Sectors

  • Pharmaceutical & Medical Devices

Shifts

  • General Shift
About Company

IT Consulting

2023-10-25
2023-12-05T18:30
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EUR

Contact us below to hear about our global solutions

marketing@techfynder.com

India : +91 9030744477

Ireland: +353 19685077

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    SUPPORT
  • FAQ
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