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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates strong technical expertise in VMS product formulation, stability, and analytical controls, while effectively managing product quality lifecycle and regulatory compliance. Capable of leading technology transfer and scale-up processes across global manufacturing sites, ensuring robust product control strategies and risk assessments.
Highest-signal resume keywords
VMS Product FormulationProduct Quality Lifecycle ManagementTechnical Risk AssessmentGlobal Regulatory ComplianceTechnology Transfer
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
VMS Product FormulationAnalytical ControlsTechnical Risk AssessmentProduct Quality Lifecycle ManagementStability TestingExcipient InteractionsRegulatory WritingGMP RequirementsScale-Up ProcessesPost-Approval Change Management
Soft Skills
Influencing OutcomesMentoringClear CommunicationStakeholder EngagementCollaboration
Industry Keywords
VMS ProductsConsumer Health ProductsFDAEU RegulationsICH GuidelinesFood SupplementsMatrixed OrganizationTechnical DocumentationSupplier QualificationLifecycle Optimization
About the role
Key responsibilities & impact- Own the end-to-end technical and quality lifecycle of global VMS products
- Ensure robust Product Control Strategies, current Technical Risk Assessments, and consistent execution across internal sites and CMOs
- Act as the global technical authority for VMS formulations, vitamins, minerals, excipient interactions, stability, and shelf-life performance
- Lead data-driven continuous improvement programs using manufacturing performance, analytical data, and stability results
- Provide technical leadership on post-approval changes, raw material changes, supplier qualification, formulation adjustments, and site transfers
- Support new product introductions and lifecycle optimization during formulation development, scale-up, and technology transfer
- Serve as the primary technical interface for Health Authority interactions and internal stakeholders
- Provide justifications related to quality, specifications, stability, and lifecycle management
- Mentor site Technical and Supply teams and build technical capability in VMS manufacturing processes, analytical controls, and product knowledge
Requirements
What you’ll need- Bachelor’s degree in science or engineering (chemistry, pharmacy, food science or related)
- Approximately 8–10 years of relevant industry experience in VMS or consumer health products
- Strong technical expertise in VMS product formulation, stability, excipient interactions, and analytical controls
- Demonstrated capability in Product Quality Lifecycle Management, including technical risk assessment, control strategies, and post-approval change management
- Experience leading technology transfer and scale-up across multiple manufacturing sites or CMOs
- Working knowledge of global regulatory and GMP requirements applicable to food supplements and VMS products, including FDA, EU, and ICH-aligned frameworks
- Experience working in a global, matrixed organization
- Ability to influence outcomes across R&D, Quality, Supply Chain, Regulatory, and Procurement without direct authority
- Ability to translate complex scientific and technical topics into clear, actionable guidance for non-technical stakeholders and senior leadership
- Experience engaging with CMOs, ingredient suppliers, scientific experts, and regulators
- Strong technical documentation and regulatory writing capability
- Experience supporting portfolio-level decision making in the VMS category
Benefits
Comp & perks- Inclusive culture where different backgrounds and views are valued and respected
- Inclusion and belonging programmes open to all Haleon employees
- Reasonable adjustments and accommodations throughout the recruitment process
- Confidential handling of personal information
- Support and assistance during the application process