SOQ Senior Manager- Export Markets and Value Maximization Group (VMG)/Responsible Person (RP)
Location
Netherlands (PEBV License)
Registered Responsible Person with Dutch Health Authorities
Role Impact
This role is critical to ensuring compliant, efficient, and uninterrupted supply across Export Markets while enabling the evolution toward a harmonized VMG operating model and strengthening the link between Quality, Regulatory, and Business objectives.
Role Summary
The Senior Manager – Export markets and VMG has dual responsibility:
VMG Quality Oversight: is responsible to Support the above‑market Quality leadership and oversight of VMG (Value Maximizing Group) markets across Europe, ensuring:
Risk‑based, compliant, and harmonized Quality operations
Strong governance and performance monitoring across VMG markets
Alignment with Pfizer Quality Standards and regulatory expectations
Acts as the Quality point of contact (POC) for VMG markets and supports the evolution of small/export markets into the VMG operating model
Export Markets Quality Oversight/RP: is responsible for maintaining an effective Quality Management System (QMS) across all Export Markets operating under the PEBV license (\+50 markets).
The role ensures that Pfizer PEBV products are managed, released, and distributed to logistics service providers (LSPs) and distributors in full compliance with EU Good Distribution Practice (GDP), Dutch Board of Health (BOH) requirements, and Pfizer Global SOPs (GSOPs).
The position serves as the designated Responsible Person (RP), acting as the primary point of contact with Dutch Health Authorities, while driving a risk\-based, harmonized, and compliant quality operating model across VMG and Export Markets.
Key Responsibilities
1\. Export Markets \& VMG Quality Oversight
Act as above\-market Quality Point of Contact (POC) for VMG and Export Markets
Ensure consistent implementation of QMS across all markets in scope
Monitor and trend quality performance, risks, and compliance signals
2\. Governance, Compliance \& Operations
Ensure oversight of distributors, LSPs, and Quality Agreements
Maintain inspection readiness and support audits and regulatory inspections
Oversee deviation management, CAPA, change control, and risk processes
Ensure traceability and compliance in repackaging/relabeling activities
Maintain and continuously improve the QMS
3\.Responsible Person (RP) Accountabilities for PEBV
Act as RP named on PEBV License
Serve as primary point of contact with Dutch Health Authorities
Ensure compliance with EU GDP and Dutch regulatory requirements at all times
Core RP Duties include:
Ensuring QMS implementation and maintenance
Oversight of authorized activities and record integrity
Approval of suppliers, customers, and subcontracted activities
Ensuring training programs are in place and effective
Managing recalls, complaints, and product disposition decisions
Approving returns to saleable stock and handling non\-conforming products
Ensuring self\-inspections and CAPA implementation
Approving SOPs and supporting complex investigations
Ensuring compliance with national regulatory requirements and license conditions
Safeguarding product quality across all distribution activities
Additional Responsibilities
*Quality Culture \& Capability Building*:
Promote strong Quality culture across markets and functions
Provide training and awareness on quality and compliance requirements
Ensure timely and right\-first\-time quality documentation
*Business Continuity*
Ensure continuous RP availability and oversight
Maintain the PEBV License
Support uninterrupted and compliant product supply
*Pharmacovigilance \& Compliance*
Ensure adherence to pharmacovigilance requirements (YRR program)
Report safety information to Drug Safety Units as required
Ensure compliance with Business Ethics and regulatory standards
Support product quarantine, recalls, and communication with LSPs
4\. Risk\-Based Performance \& Data Analytics
Consolidate and analise quality data across markets to identify trends and risks
Proactively escalate systemic issues and support risk mitigation actions
Support inspection readiness and continuous improvement initiatives
5\. VMG Model Expansion \& Integration
Support integration of small markets into the VMG operating model
Contribute to fit\-for\-purpose quality governance and oversight frameworks
6\. Harmonization \& Ways of Working
Drive harmonization of quality processes, tools, and governance
Ensure consistent application of GDP/GxP and Pfizer GSOPs
Partner with Cluster and Market Quality Leads to ensure consistent application of GxP/GDP and Pfizer Quality Standards
7\. Cross\-Functional Collaboration
Act as SOQ interface with Commercial, Medical, Regulatory Affairs, and Global Supply Chain
Support issue resolution, inspections, audits, and regulatory interactions
Qualifications \& Experience
- Bachelor’s degree in pharmacy, Science, Engineering, or related field (required)
- Advanced degree (MSc, MBA, Quality/Regulatory) preferred
- 10\+ years in Quality, Compliance, Supply Chain, or Regulatory roles within the pharmaceutical industry
- Qualified and eligible to act as Responsible Person under EU/Dutch GDP regulations
- Strong experience in GDP/GxP environments (pharmaceutical distribution/export preferred)
- Solid knowledge of EU and Dutch regulatory frameworks
- Experience interacting with Dutch Health Authorities and managing inspections
- Proven experience in multi\-market and complex supply environments
- Key Competencies: Strong balance between compliance and business priorities. Risk\-based and pragmatic decision\-making. Stakeholder engagement and influencing skills. High accountability and ownership. Ability to operate in a fast\-paced, international environment.
- Languages: Fluent in English and Dutch
Are you interested?
Do you know enough and have you decided to respond? We are curious about you and invite you to submit your application via the apply button below. The closing deadline for applications is June 7th.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
We kindly ask you to provide your application documents in English!
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Pfizer's aim is to provide equality of opportunity in the recruitment process by avoiding any bias or potential discrimination on any grounds including (but not limited to): sex, age, race, religion or belief, sexual orientation or disability. At Pfizer we are creating an organization and promoting a culture that respects each individual's unique character and life experiences and reflects the diversity of our society, customers and markets. We will achieve this through fostering and sustaining an environment in which every colleague feels valued and supported.
Disability Inclusion:
Onze missie is om de kracht van al onze mensen te ontwikkelen en ruimte te geven. We zijn trots om een inclusieve werkgever te zijn, die aan alle kandidaten met een beperking gelijke kansen biedt. We moedigen je aan om jezelf te zijn en dat met ons te delen, wetende dat wij ons best gaan doen om jouw sollicitatie en toekomstige carrière te ondersteunen. Jouw reis bij Pfizer begint hier!
Quality Assurance and Control
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