*Rate at $55/hr on C2C* Hi
Hope you are doing well I am Steven, working as a recruiter with Infotree Service Inc. I am currently working on “Sr. *Project Manager II*” position with *Medtronic* I will appreciate your response at the earliest, as the managers tend to move fast! *NOTE :** SEND RESUMES WITH THESE DETAILS , Profiles with all mandatory details would be processed with TOP Priority* *Name (First & Last)* *Contact No.* *Email ID * *Current Location* *Willing to Relocate if need* *Work Visa Status*, *Expiry Date* *Availability * How soon can you join?* *Reason for change* *Are you fine with drug and background check?* *Skype ID* *Last 4 Digit SSN No.* *DOB(Day, Month)* *Higher Education, Year of Completion * *Job Title* *Project Manager II (MDTJP00005774)* *Project Location* *Northridge, CA, 91325* *Duration* *12+ months /Contract* *Description* POSITION DESCRIPTION: The Senior Project Analyst will be responsible for cross-functional project team coordination and leadership for various projects and programs related to business unit programs and product development initiatives. Under general direction, this individual will oversee the operational aspects of ongoing projects and services as liaison between project manager and planning, project team, and line management. Will review status of projects and budgets; manage schedules and prepare status reports. Monitor the project from initiation through delivery as directed by Core Team Lead. POSITION RESPONSIBILITIES: This role will be responsible for organizing and leading interdepartmental activities which include project meetings, publishing detailed minutes consisting of action items and deliverables, developing and updating presentations for projects and program status’ in addition to ensuring completion of assigned projects to an agreed upon schedule created by key functional contributors from the team. Incumbent will: • Ensure projects are run in compliance with the Design Control SOP or their subordinate DOP’s and facilitate the completion of all Phase reviews. • Act as an interface and conduit across company-wide functional organizations to meet and facilitate compliance with required project timelines. • Interface and assist team members in achieving corporate goals and other related project tasks. • Lead projects as assigned and provide support for initiatives in various functional areas which may include field efforts and customer facing activities. This role will also have responsibilities that may include external supplier and/or customer interactions and travel through national and international markets. Examples may include working with suppliers to plan activities, develop schedules, and monitor progress as well as identifying requirements and completing specifications for future products with physicians and nurses. Other examples may include organizing, leading/ executing the logistical aspects of ongoing clinical studies working with clinical experts responsible for study compliance and regulations. Examples of projects responsibilities include: o Facilitating completion of project phases and coordinating audit activities o Maintaining strict compliance to Design Control Procedures o Creating and maintaining detailed Project Schedule(s) o Schedule and chair project meetings, and design reviews o Publish project action items and meeting minutes which track deliverables and open items o Provide input and lead team engagement and motivation strategies o Ensure project deliverables meet requirements (Regulatory, Corporate, Notified Body and UL as Required) o Providing leadership for design and development (potentially includes field research) o Updating program status reports for the leadership team for various forums o Facilitating the intervention and problem solving with project managers, line managers and team members o Interface with cross-functional groups, aligning priorities to achieve a common end goal BASIC QUALIFICATIONS: • Bachelor's degree and 5 years of engineering/project management/project analyst work experience OR Master's Degree and 3 years of engineering/project management/project analyst work experience. • Directly applicable Project/Program Management work experience within a regulated industry (e.g. medical device, aerospace/defense, automotive, pharma) • Experience leading technical projects including the management of internal and/or external resources based globally. DESIRED/PREFERRED QUALIFICATIONS • PMP certification preferred • Prior work experience in medical device preferred • Engineering or technical degree strongly preferred. • Master’s degree in relevant disciplines (MBA, MHA, MSN, etc.) • SAP and Microsoft Project experience preferred. • More than 7 years of related experience in an engineering/project analyst/project management capacity. • Functional project leadership experience. • Experience with efficiency/ workflow analysis including Six Sigma training • Excellent written and verbal communication skills; ability to present information to cross functional audiences and management. • Commitment to working in a collaborative and dynamic research field. • Strong time management and prioritization skills are required for management of multiple projects; Adaptability to rapidly changing priorities. • High degree of initiative and self motivation. • Ability to read, analyze and interpret common scientific data. • Ability to respond to common inquiries or complaints from customers. • Demonstrated ability to manage internal and external customers/vendors. *Thanks & Regards,* *Steven* - Technical Recruiter *Phone *(Direct): 734-888-8174 *Email:* ste...@infotreeservice.com <st...@infotreeservice.com> | *Website:* www.infotreeservice.com *LinkedIn:* https://www.linkedin.com/pub/steven-fernandez/104/956/240 *Hangout:* steven.usrecruiter | *Yahoo:* steven.usrecruiter *Mailing Address:* 215 Ann Arbor Rd. Suite 304 Plymouth, MI 48170 [image: Description: Description: Description: cid:image001.jpg@01D047B2.F3DC0D60] ------------------------------ “This message and any attachments are solely for the intended recipient and may contain confidential or privileged information. If you are not the intended recipient, any disclosure, copying, use, or distribution of the information included in this message and any attachments is prohibited. If you have received this communication in error, please notify us by reply e-mail and immediately and permanently delete this message and any attachments. Thank you.” -- -- To unsubscribe from this group, send email to cbe-software-engineer-unsubscr...@googlegroups.com For more options, visit this group at http://groups.google.com/group/CBE-Software-Engineer?hl=en --- You received this message because you are subscribed to the Google Groups "CBE Software Engineer" group. To unsubscribe from this group and stop receiving emails from it, send an email to cbe-software-engineer+unsubscr...@googlegroups.com. For more options, visit https://groups.google.com/d/optout.