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Manager Supplier Governance – REMOTE - (JP9808)

Charleston, SC · Biotech/Pharmaceutical
Job Title:  Manager Supplier Governance – REMOTE - (JP9808)
Location: Charleston, SC. (100% REMOTE)
Employment Type:  Contract
Business Unit: Innovation Planning and Platform Services
Duration: 6+ months (with likely extensions)
Notes:  100% Remote
Posting Date:  2/11/22

3 Key Consulting is hiring a Manager Supplier Governance for a consulting engagement with our direct client, a leading global biopharmaceutical company.

Job Description:
  • Ensure appropriate governance and oversight of suppliers.
  • Maximize the value obtained from partnerships with external providers at a study, program or supplier level
  • Key Activities:
    • Ensure quality oversight of suppliers through.
    • Providing ongoing governance oversight and encourage sharing of best practices and development of process improvements.
    • Chairing and managing supplier governance meetings.
    • Working with suppliers and internal customers (typically up to Director level) to identify, manage, escalate and resolve issues related to supplier performance.
    • Measuring supplier performance and reporting performance feedback to internal
  • Support business functions with selection and development of new suppliers by
    • Identifying business needs at client for new suppliers with functional input.
    • Supporting final decision on selection of suppliers.
    • Execute account activations and deactivations of R&D SG -managed suppliers.
  • Identify functional best practices and process improvements and coordinate their development and implementation for suppliers by
    • Communicating and standardizing best practices across supplier types.
    • Ensuring adherence to best practices by client functional areas.
    • Liaise with functional areas to ensure internal business needs are being met.
    • Contribute to, and as appropriate, lead departmental and cross-functional initiatives and special projects as identified by management or business need.
  • Responsible for:
    • Facilitating and delivering supplier governance forums and activities.
    • Developing effective partnerships with suppliers.
    • Measuring and reporting supplier performance.\
    • Financial oversight of suppliers across portfolio of work.

Why is the Position Open?
Back fill.

Top Must-Have Skill Sets:
5+ years of experience with at least 1 year of management

Day to Day Responsibilities:
  • Facilitating and delivering supplier governance forums and activities.
  • Developing effective partnerships with suppliers.
  • Measuring and reporting supplier performance.
  • Financial oversight of suppliers across portfolio of work.

Basic Qualifications:
Knowledge:
  • Experience working in a global, matrix organization
  • Professional Collaboration and Leadership skills
  • Knowledge of discovery research, Pre-clinical TOX, BioA, PK, and ADA suppliers (NICE to have)
  • Knowledge of Good Clinical Practice (GCP), Good Laboratory Practice(GLP)
  • Knowledge of FDA Regulations and guidelines
  • Familiar with International regulatory requirements/guidelines
  • Project management skills and fluent in technology tools – MS Teams, SharePoint, Office suite

Experienced with the following:
  • Oversight of supplier’s compliance to GCP and GLP regulations (Nice to have; Can also have experience working at a supplier that follows these regulations)
  • Oversight of supplier’s compliance to animal welfare (Nice to have)

Education
  • Doctorate degree OR
  • Master’s degree & 3 years of Business Professionals / Exec related experience OR
  • Bachelor’s degree & 5 years of Business Professionals / Exec related experience OR
  • Associate’s degree & 10 years of Business Professionals / Exec related experience OR
  • High school diploma / GED & 12 years of Business Professionals / Exec related experience AND
  • Previous direct managerial and/or leadership experience

Preferred Qualifications:
  • BA/BS/BSc in the sciences or RN
  • 7 years work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical research experience ( clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company

Employee Value Proposition:
The chance to extend and possibly get converted to permanent.

Red Flags:
No direct experience.

Interview process:
Phone screening followed by in-person interview.



We invite qualified candidates to send your resume to resumes@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
 
 
Regards,
 
3KC Talent Acquisition Team
 
 
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