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Tarsus Pharmaceuticals

Manager II, Quality Compliance

Posted 6 Days Ago
Be an Early Applicant
In-Office
Irvine, CA, USA
120K-168K Annually
Senior level
In-Office
Irvine, CA, USA
120K-168K Annually
Senior level
This role involves managing product quality complaints in line with GMPs, supporting audits, and ensuring compliance with regulatory standards. Responsibilities include overseeing complaint investigations, preparing reports, and supporting quality management systems.
The summary above was generated by AI

About the Role:

This position is responsible for supporting the Product Quality Complaint program and ensuring that all complaints are handled in accordance with GMPs and health authority requirements and expectations. This position will also be responsible for supporting Annual Product Reviews.  In addition, the role includes supporting other QMS areas, when needed (i.e. Audits and inspections, Change Control, Document Control, CAPA).

Let’s talk about some of the key responsibilities of the role:

  • Support of the product complaint program, from intake to closure, including:
    • Open Product Complaint Investigations
    • Liaise with Call Center staff for Product Complaint Intake
    • Follow-up directly with complainants, when necessary
    • Participate in Weekly Product Complaint Meetings
    • Prepare Response Letters to Complainants
    • Review proposed Product Complaint investigations and close the Complaints
    • Contribute Product Complaint Data to Annual Product Reviews
    • Prepare monthly complaint metrics and Management Review Presentations
    • Support Regulatory Inspections or Alliance Partner Audits, as required
    • Author/Revise or Approve Controlled Documents
  • Understand the regulatory environment and work proactively to evolve systems and procedures to ensure the product complaints are managed in accordance with company policies and government regulations.
  • Ensure monitoring and appropriate escalation of Product Complaints, including expedited complaints.
  • Support effective relationships, cooperation and alignment of objectives within Quality and with internal partners
  • Assemble Annual Product Reviews and:
    • Ensure contributing departments/partners deliver data timely
    • Prepare product complaint data/metrics for the APR
    • Ensure on time delivery of completed report
  • Assist in any Recalls or Field Alerts
  • Assist in performing Mock Recalls
  • Support other Quality Management Systems, as required:
    • Document Control, Change Control and CAPA systems
  • Perform additional duties as assigned by department management

Factors for Success:

  • Bachelor’s Degree in Scientific Field Preferred
  • 8 years’ experience in the areas of pharmaceutical Quality Assurance and Compliance:
    • Complaint Management
    • Annual Product Review
    • Document Management
    • Regulatory Inspection Support
    • Internal and External Audit Support
    • Quality Management Review
  • Attention to detail
  • Strong knowledge of Microsoft Office Systems
  • Knowledge of Other Quality Management Systems (Veeva, TrackWise, SAP, Oracle, DOT Compliance, Master Control, ComplianceWire and other LMS)
  • Decision Making - Demonstrates strong decision-making by applying structured analysis to complex challenges, balancing competing priorities and long-term impacts while engaging stakeholders and driving solutions aligned with organizational goals.
  • Collaboration and Team Building - Promotes collaboration by aligning diverse teams around shared goals, fostering healthy debate to advance outcomes, and building strong networks that strengthen organizational effectiveness and cross-team learning.
  • Outcome Driven - Demonstrates strong outcomes focus by aligning teams around shared priorities, proactively addressing risks and dependencies, and driving cross-functional accountability to sustain progress and deliver results.

A Few Other Details Worth Mentioning:

  • The position will be based in our beautiful Irvine office, complete with onsite gym, pool, snacks, drinks, and occasional catered meals. We provide a hybrid work environment.
  • We are passionate about our culture! Our Tarsans live our values of commitment to patients, empowerment to champion innovation, and teamwork to amplify impact!
  • This position reports to the Associate Director, Quality Compliance.
  • Some travel may be required – up to 10%.

At Tarsus, we understand the importance of attracting and retaining top talent. The expected base pay range for this position is $120,000 - $168,000 plus bonus, stock equity, and comprehensive benefits. The base pay range reflects the target range for this position, but individual pay will be determined by additional factors such as job-related skills, experience and relevant education or training. Our benefits include health, dental and vision insurance benefits to ensure your well-being. We believe in work-life balance and offer generous paid time off, including vacation, holidays, and personal days. For more details regarding Tarsus benefits, please visit: https://eb.alliant.com/26tarsusbenefitssnapshot.

#LI-Hybrid

Tarsus Pharmaceuticals, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

Top Skills

Compliancewire
Dot Compliance
Master Control
Microsoft Office Systems
Oracle
SAP
Trackwise
Veeva
HQ

Tarsus Pharmaceuticals Irvine, California, USA Office

15440 Laguna Canyon Rd, Irvine, CA, United States, 92618

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