Careers

Search Jobs Connect With Us

Quality Services Supervisor

Job Attributes

Job Id:

20016

Job Category:

Clinical & Life Sciences

Job Location:

West Chester, PA  19380

Security Clearance:

No Clearance

Business Unit:

Piper Companies

JOB DESCRIPTION

Piper Life Sciences is currently looking for a Quality Services Supervisor in West Chester, PA to support a cutting-edge Bio-Pharmaceutical and Medical Device Organization.

 

Responsibilities for the Quality Services Supervisor Include:

  • Primary responsibilities include ensuring the teams managing several Supplier Quality projects adhere to procedural and project driven schedules, meet project team milestones; assist with remediating issues presented by team members and support the organization with maintaining focus on each program
  • Supervise the team managing the Supplier Quality Agreement program. 
    • Ensure all Supplier Quality Agreements are reviewed and approved within the 3-year cycle.
    • Assist with resolving Quality Agreement issues presented by the team
    • Monitor and report out schedule performance on a monthly basis
    • Assist with Supplier Quality Agreement negotiations as needed.
    • Ensure all supplier assessments are executed by defined project timelines
    • Monitor tasks associated with supplier readiness are conducted at each milestone
    • Report out project status to the core team
    • Collaborate with team members to complete milestones on or before defined timelines
    • Collaborate with team members to develop procedures for project implementation.
    • Develop communication strategy for project deployment
  • Support quality initiatives such as executing CAPAs; issuing non-conformances; and inspection/audit support
  • Support update of applicable Supplier Quality Procedures and Work Instructions

 

Qualifications for the Quality Services Supervisor I Include:

  • Minimum of 3 years’ experience in a supervisory capacity
  • Minimum of 3+ years of experience in a medical device and/or pharmaceutical industry
  • Strong familiarity with ISO-13485 and FDA QSR
  • Must be able to work independently, effective with a matrixed organization and prioritize with limited supervision. Strong written and oral communication and interpersonal (listening) skills.  
  • Proficient in Microsoft Office, EtQ, knowledge of SAP
  • Three years of experience as Project Engineer, Quality Engineer, Project Manager or equivalent role within regulated industry
  • Background in Supplier Management and Process Validation / Verification
  • Understanding supplier validation procedures and execution
  • Strong Project Management skills, must understand the critical path, identify program resources, setup project plan and track execution, establish project structure and governance around critical projects.
  • Experience with Medical Device Regulatory Compliance/Regulatory Affairs.
  • Experience with Quality Agreements and negotiating with suppliers across multiple sites and business centers
  • Process Excellence Black Belt or Green Belt
  • Ability to coach and guide core team on project expectations and track progress across multiple-sites and projects
  • Ability to act as an SME in critical compliance and business processes
  • Ability to provide regular updates to Quality leadership at various forums
  • B.S. or B.A. degree or equivalent related experience

 

Compensation for the Quality Services Supervisor Includes:

  • Full Benefits Including: Health, Vision, Dental, 401k plan

Apply Now

CONTACT INFORMATION (Required)
RESUME (Required)
No file selected
x
Formats accepted: .doc / .docx / .pdf / .txt
Don't have a resume? Click here to fill out a short form.

Copy/paste your resume inside the text editor below:

ADDITIONAL INFORMATION (Required)
WORK HISTORY (Required)
Add another experience (optional)
EDUCATION (Required)
Add another degree (optional)
SKILLS (Required)
Add another skill (optional)

The following error(s) occurred:

Please wait while your job application is being processed. This may take a few moments.
New Search

Job Id:

20016

Job Category:

Clinical & Life Sciences

Job Location:

West Chester, PA  19380

Security Clearance:

No Clearance

Business Unit:

Piper Companies