What are the responsibilities and job description for the Principal Project Manager position at The Fountain Group?
The Fountain Group is currently seeking a --------Principal Project Manager for a prominent client of ours. This position is located in South San Francisco, CA. Details for the position are as follows:
Pay Range: $50 - 104/hr depending on experience
Contract: 8 months with possible extension and/or conversion
100% onsite in South San Francisco, CA
Job Description:
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Pay Range: $50 - 104/hr depending on experience
Contract: 8 months with possible extension and/or conversion
100% onsite in South San Francisco, CA
Job Description:
- Manage complex projects across the development pipeline—from initial design to post-approval—while managing the regional business and compliance activities for the Device Development. Strategic Planning: Translate device strategy into actionable plans, defining "inspection-ready" Design & Development Plans.
- End-to-End Management: Lead a range of projects including development pipelines, line extensions, and technology initiatives.
- Team Performance: Foster high-performing team dynamics, facilitating efficient decision-making, issue resolution, and cross-functional collaboration.
- Governance & Business Gates: Navigate teams through business process stage-gates and support technical advisory or governance committee reviews.
- QMS Implementation: Drive implementation, maintenance, and continuous improvement of the Quality Management System (QMS) including the tracking of metrics
- Records Management: Manage Design History Files (DHF) and document repositories to ensure accuracy, completeness, and regulatory compliance.
- Audit Readiness: Manages audit and inspection readiness, including preparation for internal audits and Health Authority inspections, and oversees timely remediation of findings.
- Education: B.S. degree in Engineering, Technical Field, or a related discipline.
- Experience: At least 12 years in the Pharmaceutical or Medical Device industry.
- Minimum 5-6 years specifically in medical devices or combination products.
- Proven experience in drug/device development and commercialization.
- Regulatory Expertise: Extensive knowledge of EU MDR, FDA 21 CFR Parts 210, 211, & 820 (including 820.30 design controls), and ISO 13485.
- Project Management: Proficiency in PM best practices and software; PMP certification is considered a significant asset.
Please forward this email to any friends or colleagues as we do offer a Referral Bonus for any candidate hired.
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at Privacy Policy
#ZIP
Salary : $50 - $104