Icon hamburger
US
What job do you want?
Apply to this job.
Think you're the perfect candidate?
Apply Now
Thumsup

You’re being taken to an external site to apply.

Enter your email below to receive job recommendations for similar positions.
Default1

Sr Program Manager/Liaison

Marion Full-Time
$194,133.00 (Careerbuilder est.)
Apply Now


Client Position Title: Program Manager/ Liaison

Position Number: 327597

Location: Marion, NC 28752

Desired Skill Set:

Program Manager, FDA, Engineer, GMP

Position Description:

**C2C is not available**
**Only U.S. Citizens and those authorized to work in the U.S. can be considered as W2 candidates.**

Job Title: Sr Program Manager/Liaison

Start Date: 10/21/2019
End Date: 10/19/2020
Location: Marion, NC 28752

Job Title: Program Manager/Liaison

Summary
The Program Manager for FDA Remediation Major Capital Projects will function as the owner representative on major capital projects associated with remediation while providing consulting, engineering and facilities project management services.
Responsibilities
• Independently plan, execute and direct cross functional engineering projects, that may cross traditional product lines. Seek diverse new approaches to problems encountered through adaptation and modification of standard engineering principles.
• Manage projects on a cross functional basis, including direct supervision of team members.
• Manage the project costs (all financial aspects) of product development. This will include capital expenditures and cross functional expenses.
• Identify and resolve complex problems, including the development of new design of experiments, without supervision.
• The following projects and associated work have been identified but can be adjusted based on client needs.
• Water for Injection (WFI) system
• Solution Transmission System (STS)
• CIP Systems associated with STS

• Participate in operational meetings with Leadership Team for project performance and financial metrics.
• Preparation of FDA and Senior Leadership communications and presentations.
• Additional engineering consulting/support service requested by the client.
• Qualifications
• Certified Project Management Professional (PMI or IPMA or equivalent certification) required
• Business acumen
• Competent application of Baxter's Vital Behaviors and Leadership Essentials
• Understanding of Good Manufacturing Practices
• Demonstrated competencies in all aspects of project management
• Ability to develop others
• Good communication skills with matrix management experience required
• Independent judgment in the evaluation, selection and adaptation of various engineering techniques required
Education/Experience
• Minimum of a completed Bachelor of Science in Engineering or Science discipline
• At least 8-10 years relevant experience; plus, an additional 2-5 years of matrix management experience
• Microsoft Word, Excel, Outlook, PowerPoint, and Project preferred
• Previous regulated industry experience strongly preferred
• Previously experience working on an FDA Remediation project(s), preferred
• Physical Requirements (Large manufacturing site)
• Requires continuous grasping, pushing/pulling up to 15 pounds and reaching with hands and arms
• Lifting and carrying on average up to 15 pounds frequently throughout the shift
• Can complete quick and precise repetitive processes using both arms and both hands
• Occasionally specialized physicals are required when working with certain drug codes
• 


Education/Experience
• Minimum of a completed Bachelor of Science in Engineering or Science discipline
• At least 8-10 years relevant experience; plus, an additional 2-5 years of matrix management experience






Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.)



Recommended skills

Engineer
Fda
Gmp
Program Manager
Communication
Leadership

Location

CareerBuilder Estimated Salary What is the Careerbuilder Estimated Salary? Only about 20% of the jobs in our search results contain salary information. When a job posting doesn’t include a salary, we estimate it by looking at similar jobs in the same industry in that location. It is not necessarily endorsed by the employer and actual compensation may vary based on your experience.

x

What is the Careerbuilder Estimated Salary?

Only about 20% of the jobs in our search results contain salary information. When a job posting doesn’t include a salary, we estimate it by looking at similar jobs in the same industry in that location. It is not necessarily endorsed by the employer and actual compensation may vary based on your experience.
This estimation is based on Job title, Industry, Location and Skills
$194,133
Avg. Yearly Salary
Apply to this job.
Think you're the perfect candidate?
Apply Now

Help us improve CareerBuilder by providing feedback about this job: Report this job

Report this Job

Once a job has been reported, we will investigate it further. If you require a response, submit your question or concern to our Trust and Site Security Team

Job ID: 327597

CAREERBUILDER TIP

For your privacy and protection, when applying to a job online, never give your social security number to a prospective employer, provide credit card or bank account information, or perform any sort of monetary transaction. Learn more.

By applying to a job using CareerBuilder you are agreeing to comply with and be subject to the CareerBuilder Terms and Conditions for use of our website. To use our website, you must agree with the Terms and Conditions and both meet and comply with their provisions.