Blue Star Partners, LLC
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Project Manager I
role at
Blue Star Partners . Get AI-powered advice on this job and more exclusive features. Job Details Job Title:
Project Manager I Location:
Santa Clara, CA onsite local candidates only Period:
09/02/2024 to 09/01/2025 possibility of extension Hours/Week:
40 hours hours over 40 paid at time and a half Rate:
$45 - $50/hour Contract Type:
W-2 only
Scope of Services
The Project Manager I oversees activities and personnel involved in small to large-scale projects, primarily focusing on non-IT business applications and disciplines. Responsibilities include managing all aspects of projects throughout the full lifecycle, collaborating with stakeholders, defining project scope, developing initiatives, and ensuring project success within budgets and timelines. Experience with medical devices, clinicals, design controls, and working in regulated environments is essential. The role also involves supporting IVDR compliance activities, including technical files, post-market surveillance, and regulatory support tasks. Responsibilities and Deliverables Manage activities and personnel for projects focusing on non-IT applications. Handle all facets of multiple projects through their full lifecycle. Collaborate with sponsors, business units, and users to define project scope and develop plans. Guide and monitor project staff for successful task execution. Deliver high-quality solutions within budgets and timelines. Provide guidance and support throughout projects. Track, report, and present project status to management and stakeholders. Demonstrate experience with medical devices, clinicals, and design controls. Lead cross-functional teams in science, lab, or clinical settings with strong interpersonal skills. Support IVDR compliance activities and regulatory documentation. Perform on-market support tasks such as regulatory impact assessments and license updates. Preferred: understanding of diagnostic assays.
Qualifications
Bachelor's degree in a relevant field. PMP certification is required. 1-6 years of project management experience. Experience with medical devices and cross-functional teams in clinical/science environments. Excellent interpersonal and negotiation skills. Preferred: knowledge of diagnostic assays.
Additional Details
Seniority level: Mid-Senior level Employment type: Full-time Job function: Project Management and IT Industries: Business Consulting and Services
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Project Manager I
role at
Blue Star Partners . Get AI-powered advice on this job and more exclusive features. Job Details Job Title:
Project Manager I Location:
Santa Clara, CA onsite local candidates only Period:
09/02/2024 to 09/01/2025 possibility of extension Hours/Week:
40 hours hours over 40 paid at time and a half Rate:
$45 - $50/hour Contract Type:
W-2 only
Scope of Services
The Project Manager I oversees activities and personnel involved in small to large-scale projects, primarily focusing on non-IT business applications and disciplines. Responsibilities include managing all aspects of projects throughout the full lifecycle, collaborating with stakeholders, defining project scope, developing initiatives, and ensuring project success within budgets and timelines. Experience with medical devices, clinicals, design controls, and working in regulated environments is essential. The role also involves supporting IVDR compliance activities, including technical files, post-market surveillance, and regulatory support tasks. Responsibilities and Deliverables Manage activities and personnel for projects focusing on non-IT applications. Handle all facets of multiple projects through their full lifecycle. Collaborate with sponsors, business units, and users to define project scope and develop plans. Guide and monitor project staff for successful task execution. Deliver high-quality solutions within budgets and timelines. Provide guidance and support throughout projects. Track, report, and present project status to management and stakeholders. Demonstrate experience with medical devices, clinicals, and design controls. Lead cross-functional teams in science, lab, or clinical settings with strong interpersonal skills. Support IVDR compliance activities and regulatory documentation. Perform on-market support tasks such as regulatory impact assessments and license updates. Preferred: understanding of diagnostic assays.
Qualifications
Bachelor's degree in a relevant field. PMP certification is required. 1-6 years of project management experience. Experience with medical devices and cross-functional teams in clinical/science environments. Excellent interpersonal and negotiation skills. Preferred: knowledge of diagnostic assays.
Additional Details
Seniority level: Mid-Senior level Employment type: Full-time Job function: Project Management and IT Industries: Business Consulting and Services
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