Microbiology Expert – Small Molecules
Il y a 4 jours
Beerse Flemish Region, VLG, Belgique
Pauwels Consulting
Temps plein
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Our client, a global pharmaceutical leader, is seeking a Microbiology Expert – Small Molecules to support clinical and lifecycle management programs. This role involves coordinating global microbiology activities and providing scientific expertise in method qualification and validation within an R&D environment.
Responsibilities
- Lead and coordinate microbiology-related R&D and Lifecycle Management projects for Small Molecule products.
- Provide scientific input on microbiological method development, qualification, validation, and specification setting.
- Act as project lead for global method transfer and harmonization activities across various sites and external partners.
- Review and approve development reports, validation documentation, and microbiological test methods including sterility, bioburden, and bacterial endotoxin.
- Coordinate and follow up on Change Controls and specification documents within the microbiology domain.
- Ensure compliance with all relevant GMP, GxP, and regulatory standards. Requirements
- Master's degree in Pharmaceutical Microbiology, Life Sciences, or a related field.
- You have 3+ years of experience in a GMP-regulated pharmaceutical environment.
- You possess profound knowledge of pharmaceutical microbiology including contamination control, sterility assurance, bioburden, and bacterial endotoxin.
- You bring expertise in microbiological method validation, method qualification, and method transfer.
- You have experience with Small Molecules and techniques such as PET/AET, ATP bioluminescence, and microbial purity.
- You possess strong project management skills and the ability to influence stakeholders in a global matrix organization.
- You are fluent in English. Nice to Haves
- Experience with quality management systems or document control software.
- Interest in contributing to R&D projects and continuous strategy improvement.
- Lead and coordinate microbiology-related R&D and Lifecycle Management projects for Small Molecule products.
- Provide scientific input on microbiological method development, qualification, validation, and specification setting.
- Act as project lead for global method transfer and harmonization activities across various sites and external partners.
- Review and approve development reports, validation documentation, and microbiological test methods including sterility, bioburden, and bacterial endotoxin.
- Coordinate and follow up on Change Controls and specification documents within the microbiology domain.
- Ensure compliance with all relevant GMP, GxP, and regulatory standards. Requirements
- Master's degree in Pharmaceutical Microbiology, Life Sciences, or a related field.
- You have 3+ years of experience in a GMP-regulated pharmaceutical environment.
- You possess profound knowledge of pharmaceutical microbiology including contamination control, sterility assurance, bioburden, and bacterial endotoxin.
- You bring expertise in microbiological method validation, method qualification, and method transfer.
- You have experience with Small Molecules and techniques such as PET/AET, ATP bioluminescence, and microbial purity.
- You possess strong project management skills and the ability to influence stakeholders in a global matrix organization.
- You are fluent in English. Nice to Haves
- Experience with quality management systems or document control software.
- Interest in contributing to R&D projects and continuous strategy improvement.