Analytical QC Portfolio Lead – R3, R4 Level

Pfizer

Quality Control Portfolio Lead ensuring QC deliverables for Analytical Research & Development projects. Collaborating across teams and monitoring product stability while authoring regulatory submissions.

Posted 7/14/2026full-timeAndover • Massachusetts, Montana • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Quality Control within Analytical Research & Development, effectively managing project deliverables and timelines while ensuring product quality and compliance. Strong ability to communicate complex technical concepts and collaborate across diverse teams to achieve project objectives.

Highest-signal resume keywords

Quality Control ExpertiseProject Management SkillsStrong Communication SkillsAnalytical Research & Development ExperienceTime Management Skills

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Quality ControlProject ManagementData AnalysisTechnical WritingProduct Stability MonitoringInvestigation ManagementRegulatory ComplianceTrend EvaluationOOS/OOT InvestigationCross-Functional Collaboration

Soft Skills

Self-AccountabilityAttention to DetailCollaborationAdaptabilityProblem-Solving

Industry Keywords

Analytical Research & DevelopmentHealth Authority ComplianceTechnology TransferProject GovernanceMatrix Environment

About the role

Key responsibilities & impact

Serve as a single point of contact representing QC on Analytical Research & Development (ARD) project sub-teams
Ensure project progression and deliverables are met
Liaise between ARD Sub-team and the QC functions to facilitate project progression
Collaborate with cross-functional roles including the ARD, PhRD, and BRD Leads
Monitor product stability and evaluate trends and product quality changes
Authoring responses to Health Authority information requests pertaining to QC
Lead and support product-related investigations such as OOS/OOT as QC SME
Represent QC in technology transfer teams and at applicable project governance meetings

Requirements

What you’ll need

Applicant must have a bachelor's degree with at least 6+ years of experience
Scientific excellence demonstrated in a Quality Control functional role
Experience representing one or more QC functions on a project team with defined objectives and endpoints
Able to manage diverse activities to deliver on milestones according to set timelines
Able to collaborate and maintain self-accountability in a matrix environment
Strong communication skills, able to present complex technical concepts to enable understanding by colleagues from all disciplines / all levels
Strong project management skills and experience managing multiple projects at the same time is essential
Strong time management skills with attention to detail and desire to achieve team and individual goals.

Benefits

Comp & perks

Eligible for Relocation Package – NO
Secondment 12 months
Flexible, and colleagues are expected to comply with Log In For Your Day (LIFYD) requirements at site location (e.g. about 2.5 days a week in office)