*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





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