Senior Corporate Quality Risk Management Supervisor

Tabuk Pharmaceuticals Manufacturing Company; Dammam; On-site; SAR 300,000 - 420,000; Full time

Job summary

Tabuk Pharmaceuticals Manufacturing Company seeks an experienced Corporate Senior Quality Risk Management Supervisor to lead risk-based quality oversight across sites, projects, and upgrades.

The role requires proven QRM leadership within a multinational, EU GMP, or US FDA-regulated setting, with expertise in quality systems, data integrity, and project execution. Strong collaboration across functions is essential for success.

Qualifications

• Experience in leading QRM activities within a multinational, EU GMP, or US FDA-regulated setting.
• Proven ability to design, implement and govern risk management across quality systems.
• Strong collaboration and cross-site leadership in highly regulated pharma environments.

Responsibilities

• Design, maintain and implement harmonized policies and tools for Quality risk management.
• Align with ICH Q9/Q9(R1), EU GMP, US FDA expectations and data integrity standards.
• Create a certification process for QRM champions across corporate functions and sites.
• Embed risk management in non-conformance, change control, investigations, and QA systems.
• Lead QRM for major projects such as new facilities or lines and drive remediation plans.
• Promote digital QMS, risk-based workflows, analytics, and performance dashboards.

Skills

Quality Risk Management

Regulatory Compliance

GxP Quality Systems

Quality Assurance Leadership

Data Integrity

Education

Bachelor's degree in Pharmaceutical Sciences / Engineering / Chemistry / Microbiology

Job description

We are seeking an experienced Corporate Senior Quality Risk Management Supervisor to lead risk-based quality oversight across pharmaceutical manufacturing sites, projects, and facility upgrades.

The successful candidate will have proven experience in a multinational, EU GMP, or US FDA-regulated pharmaceutical manufacturing organization, with strong expertise in Quality Risk Management, Compliance, qualification, validation, and project execution.

Key Responsibilities:

• Design, maintain and ensure implementation of harmonized corporate policies and tools related to Quality risk management
• Ensure alignment with ICH Q9/Q9(R1), ISPE, EU GMP, US FDA expectations, Annex 1, contamination control, data integrity, and GxP computerized-system requirements.
• Design and implement a certification process for QRM champions across corporate functions and sites
• Assess all Quality management systems and ensure that Risk management is embedded with the process and systems such as non-conformance, change management, internal audits, investigations, supplier qualification etc.
• Ensure that all major systems are assessed for any potential risk of failures and the appropriate risk mitigation actions are identified, implemented and effective.
• Leading QRM activities for major projects such as new facilities, and new lines
• Develop and execute remediation plans with clear milestones, accountable owners, risk controls, effectiveness checks, and sustainable closure.
• Support quality transformation programs focused on:
• Simplification and harmonization of global quality processes.
• Strengthening quality culture and management ownership.
• Digital QMS, risk-based workflows, data analytics, and performance dashboards.
• Improved right-first-time performance, inspection readiness, and operational resilience
• Facilitate and review risk-based assessments.
• Support risk assessments for deviations, CAPA, change controls, OOS/OOT investigations, complaints, recurring events, and inspection readiness.
• Promote responsible adoption of digital QRM/eQMS tools, analytics and dashboards, AI-assisted risk identification, digital validation, automation, smart manufacturing, and sustainable facility design, with appropriate governance, validation, human oversight, and data-integrity controls.

Required Experience and Qualifications:

• Bachelor's degree in Pharmaceutical Sciences, Engineering, Chemistry, Microbiology, or a related discipline.
• Typically, +12 years of relevant pharmaceutical experience in Quality, Validation, Engineering, Technical Operations, or GMP projects.
• Proven experience leading and governance of QRM activities within a reputable pharmaceutical manufacturing organization, preferably a multinational, EU GMP, or US FDA-regulated company.
• Demonstrated experience with new facilities, major facility upgrades, new production or packaging lines, critical utilities, and technology transfer projects.
• Strong working knowledge of GMP, pharmaceutical quality systems, validation, contamination control, data integrity, and risk-based decision-making.
• Experience in sterile, aseptic, biologics, non-sterile, high potent & other highly regulated manufacturing is highly desirable.
• Excellent facilitation, technical writing, stakeholder-management, influencing, and cross-site leadership skills.