Job Opportunity:
Filling Line Specialist
Lead a project to ensure compliance with good manufacturing practices, EU and FDA regulations, and company policies.
Key Responsibilities:
* Develop and execute CQV testing documentation for filling line systems, including syringe and vial lines/isolators, lyos, and associated equipment.
* 100% responsible for meeting key project deliverables for safety, CQV schedule, and quality of project-related documentation/electronic records for equipment and utilities assigned.
* Analyze data to identify potential risks during commissioning and qualification phases.
Required Skills & Qualifications:
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• A minimum of 3-5 years of experience in the pharmaceutical industry with familiarity with sterile drug product filling line experience.•
div>• A degree in a scientific or technical discipline (BS).,