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Sandoz

Leader in generic and biosimilar medicines

Quality System & Compliance Manager

Regulatory & Quality (Life Sciences)Updated on Nov 12
Full-timeGebze, Kocaeli, TürkiyeNo salary listedIn-person

About the Job

Requirements

  • Industry or business exposure.
  • Functional breadth.
  • Experience collaborating across boundaries.
  • Operations management and execution experience.
  • People leadership experience.
  • Project management experience.
  • Agility.
  • Audit management.
  • Business acumen.
  • Business partnering.
  • Collaboration.
  • Communication skills.
  • Continuous learning.
  • Ability to deal with ambiguity.
  • Decision-making skills.
  • Goal-oriented approach.
  • Knowledge of guidelines.
  • Inspection preparedness.
  • Leadership.
  • Logical thinking.
  • Problem-solving skills.
  • Quality Assurance (QA).
  • Quality decision-making.
  • Quality management.
  • Knowledge of regulations.
  • Self-awareness.
  • Stakeholder management.
  • Teamwork.
  • Technological expertise.
  • English language proficiency.

Responsibilities

  • Lead the QA function to ensure processes, procedures, tasks, responsibilities, and projects comply with pharmaceutical laws, the Sandoz Quality Manual and Policies, industry best practices, and applicable GxP requirements.
  • Implement applicable Quality Standards and governance processes through the Sandoz Quality Manual and Policies.
  • Ensure regulatory controls are in place in relevant process steps and ensure adherence to GxP, legal and internal regulations for manufacturing, control and distribution operations, and HSE requirements.
  • Implement defined Key Quality Indicators (KQIs) to monitor ongoing process control and compliance, and regularly review and assess KQIs at Leadership Team level.
  • Escalate issues appropriately, support timely resolution, provide quality oversight for deviations, and ensure corrective and preventive actions (CAPAs) are implemented.
  • Provide quality oversight for planned changes.
  • Prepare for, manage, and follow up on regulatory inspections within the area of responsibility.
  • Ensure communication of local Health Authority matters within the organization and track commitments through timely closure.
  • Implement adequate training for GxP activities within the area of responsibility by defining, planning, and supporting training activities.
  • Ensure processes communicate country-specific requirements to regional and headquarters organizations for all GxP areas, and assess implications for compliance of existing processes and systems.
  • Initiate remediation activities as necessary to ensure ongoing compliance.
  • Ensure adequate processing of complaints.
  • Establish an efficient recall organization and develop talent within the local Quality unit.
  • Develop adequate succession candidates for the Quality organizations.
  • Report technical complaints, adverse events, and special case scenarios related to Sandoz products within 24 hours of receipt.
  • Distribute marketing samples where applicable.
  • Track implementation of issued Quality Manual modules, monitor performance against KQIs, deliver the Quality Plan and budget, and monitor the number and severity of GxP issues identified during internal and external audits.

About the Company

Sandoz

Leader in generic and biosimilar medicines

What does the company do? Sandoz is a global leader in generic and biosimilar medicines, with a broad portfolio of about 1,300 products that address diseases from the common cold to cancer. How does its product work? The medicines are off-patent (generics) or biosimilars that match the reference brands in safety, quality, and efficacy, offering affordable treatment options to patients and helping healthcare systems save money while expanding access. How is it different from competitors? Sandoz emphasizes scale, a long heritage dating back to 1886, and a sizeable global workforce dedicated to broadening patient access, aiming for large social impact and substantial healthcare savings. Its leadership in biosimilars and the breadth of its portfolio set it apart in the market. What is the company's goal? To pioneer access for patients by making high-quality medicines more affordable and widely available worldwide.

Company size
10,001+
Company stage
IPO
Headquarters
Basel, Switzerland
Founded
1886

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