QC Laboratory Measurement Orchestrator (LMO) Project Deployment (Secondment / 6-12 Months)

Pfizer•Kalamazoo, MI

6d•Onsite

About The Position

The LMO Project Secondment role supports the implementation of the Laboratory Measurement Orchestrator within QC Laboratories, with a primary focus on development and deployment of Smart Document System (SDS) forms utilizing LMO connections to laboratory equipment. This role will work closely with SMEs, Quality, and Digital teams to enable transition from paper and legacy systems (e.g., PLOG/PDOCS) to compliant, data-integrated digital workflows. The position is execution-focused and centered on building, qualifying, and enabling SDS solutions that enhance data integrity, and streamline laboratory operations.

Requirements

Must have a bachelor's degree with 0+ years of experience; OR an associate's degree with 4 years of experience; OR a high school diploma (or equivalent) and 6 years of relevant experience
Working knowledge of GMP and data integrity principles
Experience in laboratory or quality systems within a regulated environment
Strong organizational and project coordination skills
Execution & Ownership – Ability to drive deliverables and manage multiple workstreams independently
Technical Acumen – Understanding of SDS form logic, data flows, and lab system integration concepts
Quality & Compliance Mindset – Strong focus on GMP, data integrity, and inspection readiness
Collaboration – Effective partnership with lab SMEs, Quality, and Digital teams.
Communication – Clear, concise updates to stakeholders and leadership.
Candidates must be authorized to be employed in the U.S. by any employer.
This position requires permanent work authorization in the United States.

Nice To Haves

Experience with SDS, PLOG, PDOCS, or digital logbook/form systems
Familiarity with laboratory instrumentation and system integrations (e.g., LIMS, LMO, Empower, etc.)
Experience in form development, system validation, or digital transformation initiatives
Understanding of Revolution, GSOPs, and computerized system compliance

Responsibilities

Partner with QC labs and SMEs to identify, prioritize, and scope SDS form opportunities, particularly those leveraging LMO integrations
Translate business needs into functional SDS design requirements
Develop and track project timelines, deliverables, and risks for assigned workstreams
Build and configure SDS forms, including logic, workflows, formulas, and equipment integrations (LMO connections)
Collaborate with SMEs to ensure forms are fit-for-purpose, user-friendly, and aligned with lab workflows
Perform testing and refinement to ensure right first-time execution and data capture accuracy
Support generation and execution of validation/qualification documentation (e.g., protocols, traceability, testing)
Ensure all SDS configurations meet GMP, data integrity, and Part 11 requirements
Partner with Quality and Digital to support change control and validation readiness activities
Facilitate training sessions for authors, reviewers, and end users within QC laboratories
Support development of training materials, user guides, and job aids
Act as a point-of-contact for user support during deployment and early adoption
Provide regular updates to stakeholders and leadership on project progress, risks, and milestones
Maintain clear communication across QC labs, Quality, Digital, and project teams
Support alignment with broader SDS and digital transformation efforts
Identify opportunities to expand SDS use cases within labs, particularly through automation and system integration
Capture feedback and drive iterative improvements to SDS forms and workflows
Support sustainability of deployed solutions through documentation and knowledge transfer