• Find preferred job with Jobstinger
  • ID
    #46886508
  • Job type
    Permanent
  • Salary
    competitive
  • Source
    Real Staffing
  • Date
    2022-11-02
  • Deadline
    2022-12-31
 
Permanent

Role Responsibilities Include:
  • Manages investigations support for product NCMRs, CAPAs and Complaints.
  • Managing daily quality control operations in support of manufacturing goals and company objective, including oversight of post-market regulatory review, and reporting to the appropriate regulatory bodies for escalated complaints.
  • Ensures accurate documentation of the complaint evaluation and investigation results within assigned complaint records
  • Manage QC testing, QC Analyst and Product Support departments

  • Primary lead in investigations from complaints including analysis of Quality System documents and process, final review, and generate/submit reports to appropriate notified bodies
    Primary lead in managing internal audit process, including performing distributor audits according to requirements and regulations
  • Support developing quality systems to ensure new systems and system changes are up to date for improvements
  • Responsible for meeting production schedules, supporting product transfers and V&V activities
  • Ensures that investigations into product performance are compliant with all required FDA, ISO and other applicable regulatory agency standards and documentation
  • Develops and initiates policies and/or procedures for continuous improvement of quality metrics
  • Act as an SME for QC responsibilities in both external and internal regulatory audits.

  • Managed the product stability program using quality metrics and performance trending activities
  • Ensures that the test processes are set-up and operating

  • Provide leadership to assigned staff and supervisors by communicating and providing guidance towards achieving department objectives

Qualifications:
  • Bachelor's degree in Chemistry, Biology, Engineering, or any Life Sciences degree
  • 8+ years of testing, analysis, compliant investigation, or quality control/assurance experience required
  • 5+ years of experience in a supervisory/management role in laboratory environment highly preferred
  • Full Knowledge/understanding of FDA regulated industry- such as ISO 13485, ISO 14971, 21 CFR Part 820, and other applicable regulations and standards
  • Experience in working with semi-automated equipment
  • Ability to perform laboratory operations with a high degree of skill, efficiency, and professionalism
  • Understanding of manufacturing systems (documentation, compliance, inventory control, production scheduling/controls, etc.).
  • Excellent written and verbal communication skills
  • Understands functionality of manufacturing equipment and operating systems

EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

To find out more about Real please visit

Report job

Related Jobs

Jobstinger