| Opening for SR PM with Validation experience in Medical device domain in CA at Foster City, California, USA |
| Email: [email protected] |
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http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=2243400&uid= Hi, I hope you are doing well, A brief version of the job description is attached below, if you are interested revert to my mail with your updated resume Role: Sr Project Manager with Validation experience in Medical device domain. Location: Foster City, CA - Onsite (5 days) Duration: Long Term Rate: $60 to 65/hr on C2C - negotiable Need PP number no opt and cpt and h1t visas and GC 1 st choice is locals, if not look for candidates who can relocate. Job Responsibilities Develop and maintain comprehensive project plans, including timelines, milestones and resource allocations Coordinate project activities, ensuring alignment with overall project goals and objectives Monitor progress against plan, identify potential risk and issues, and implement appropriate mitigation strategies. Effectively communicate ideas, project goals, and results to team members across functions and departments, including device development, packaging, quality, regulatory affairs and manufacturing. Communicate regularly with key stakeholders, including project sponsors, senior management and external partners or customers. Identify opportunities for process improvement and optimization. Qualified candidates should be self-motivated and organized, knowledgeable of relevant scientific literature, passionate about scientific inquiry and investigation, proactive in identifying and addressing potential challenges, and collaborative in driving solutions. Required Education, Experience & Skills A B.S. degree in mechanical engineering, chemical engineering, bioengineering, or a related scientific field with 8+ years of relevant experience, OR a M.S. degree with 6+ years of relevant experience. Strong verbal, written, and interpersonal communication skills are required. Ability to effectively collaborate with cross-functional teams and influence key stakeholders. Must be able to exercise judgment within well-defined and established procedures and policies in order to determine and take appropriate action. Experience in the pharmaceutical or biotechnology industry is preferred Medical device or combination product experience is preferred PMP certification is preferred -- Keywords: information technology green card California Opening for SR PM with Validation experience in Medical device domain in CA [email protected] http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=2243400&uid= |
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| 01:42 AM 11-Mar-25 |