Detalles de la oferta

Project Manager to lead and manage projects in the aseptic areas, particularly in the development, validation, and FDA submission processes for pharmaceutical and medical device products.

Responsibilities:
Develop project timelines, resource allocation plans, and budgets, ensuring timely and on-budget delivery.
Coordinate and oversee all stages of project execution from design, development, and validation through to FDA submission.
Lead and manage complex projects related to the development, commissioning, process development and validation of aseptic pharmaceutical or medical device products.
Ensure compliance with FDA and other regulatory bodies' requirements, particularly in aseptic areas and sterile manufacturing processes.
Prepare and review documentation for FDA submissions and other regulatory filings.
Requisitos:
Bachelor's degree in Engineering, Life Sciences, or a related field (Master's degree preferred).
8+ years of experience in project management in a regulated pharmaceutical, biotechnology, or medical device industry, with a focus on aseptic areas and FDA submissions.
PMP certified preferable.
Proven track record of leading projects through FDA submissions.
Strong knowledge of FDA regulations (CFR Part 210/211, 21 CFR Part 820), aseptic processing, validation protocols, and good manufacturing practices (GMP).
Experience with process validation, cleaning validation, and equipment qualification in aseptic manufacturing.


Salario Nominal: A convenir

Fuente: ClasificadosOnline

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