Project Manager - Contractor
BMA Group Panama, Dorado, Dorado, United States
Job Title: Project Manager (Contractor – 6 Months)
Location: Dorado
Function: Cross-Functional / Enterprise Programs
Description
Lead and manage strategic, cross-functional projects with high operational impact, ensuring successful execution of new product initiatives. Responsible for driving project performance from initiation to completion, aligning timelines, cost, and technical deliverables while fostering collaboration across teams.
Key Responsibilities
Define project scope, goals, timelines, resources, and risk plans.
Lead cross-functional teams across multiple projects and sites.
Manage full project lifecycle: initiation, planning, execution, monitoring, and closure.
Oversee value improvement initiatives and ensure alignment with project objectives.
Ensure adherence to processes, documentation standards, and best practices.
Facilitate communication between stakeholders and leadership; lead project reviews.
Monitor progress, identify risks/issues, and implement corrective actions.
Requirements
5+ years of experience in manufacturing, quality, or engineering within regulated industries (e.g., medical devices, pharma, biotech).
Strong knowledge of FDA regulations, GMP, and ISO standards.
Experience with new product introduction (NPI/NPD), validation, and process development.
Background in risk management, CAPA, and root cause analysis.
Proven ability to collaborate across Operations, Quality, Regulatory, R&D, and Supply Chain.
PMP certification preferred.
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Location: Dorado
Function: Cross-Functional / Enterprise Programs
Description
Lead and manage strategic, cross-functional projects with high operational impact, ensuring successful execution of new product initiatives. Responsible for driving project performance from initiation to completion, aligning timelines, cost, and technical deliverables while fostering collaboration across teams.
Key Responsibilities
Define project scope, goals, timelines, resources, and risk plans.
Lead cross-functional teams across multiple projects and sites.
Manage full project lifecycle: initiation, planning, execution, monitoring, and closure.
Oversee value improvement initiatives and ensure alignment with project objectives.
Ensure adherence to processes, documentation standards, and best practices.
Facilitate communication between stakeholders and leadership; lead project reviews.
Monitor progress, identify risks/issues, and implement corrective actions.
Requirements
5+ years of experience in manufacturing, quality, or engineering within regulated industries (e.g., medical devices, pharma, biotech).
Strong knowledge of FDA regulations, GMP, and ISO standards.
Experience with new product introduction (NPI/NPD), validation, and process development.
Background in risk management, CAPA, and root cause analysis.
Proven ability to collaborate across Operations, Quality, Regulatory, R&D, and Supply Chain.
PMP certification preferred.
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