Open since Mar 2026
Document and Data Control Manager - Project Farma
AI Summary
Manages document control, data governance, and information flow for capital projects and CQV engagements in life sciences environments, ensuring compliance and smooth handoff to operations.
About this role
When joining PerkinElmer, you select an experienced and trusted leader in scientific solutions, with the support of a global service network and distribution centers, providing the right solution, at the right time, to meet critical customer needs. With over an 80+ year legacy of advancing science and a mission of innovating for a healthier world, our dedicated team collaborates closely with commercial, government, academic and healthcare customers to deliver our broad portfolio of analytical solutions, and OneSource services.
Job Title
Document and Data Control Manager - Project Farma
Location(s)
Customer Site - PAJob Description
This is a full-time salaried position with Project Farma, a PerkinElmer company. The successful candidate will reside in the Philadelphia, PA market and be willing to travel domestically, to meet client project requests.
TheDocument and Data Control Manageris responsible foroverseeing document management, project data governance, and information flow across capital projects and CQV engagements within life sciences environments.
In this client-facing role, the manager ensures that project data, documentation, and technical drawings are properly collected, managed, and controlled throughout the project lifecycle. This includesestablishingdocument management processes, ensuring compliance with regulatory and client standards, and supporting project teams in deliveringaccurateand complete project documentation.
TheDocument and Data Control Managerpartners with project leadership, engineering teams, and clients to ensure that documentation supports project execution, qualification activities, and the long-term lifecycle management of facility assets. This role also contributes to operational excellence, client satisfaction, and delivery of Project Farma’s Patient Focused and People First culture.
Key Responsibilities
Document & Data Management Strategy
Develop and implement document and data management strategies for capital projects and CQV engagements.
Establish andmaintaindocument control procedures aligned with client requirements, regulatory expectations, and ProjectFarmabest practices.
Ensure project documentation is deliveredin accordance withproject specifications, procedures, and planning documents.
Develop and manage project information management plans governing documentation, drawings, and project data.
Project Information Management
Manage the flow of project information between clients, engineering partners, and project stakeholders.
Collect, organize, andmaintainrequired project documentation to support project delivery, qualification, and lifecycle management of assets.
Develop andmaintainmetrics to track documentation status, completeness, and quality.
Manage electronic databases and document repositories used for project documentation.
Ensure documentation is properly structured within electronic systems and hard-copy repositories whererequired.
Ensure smooth transition of project documentation and drawings from project execution to site operations.
Stakeholder Coordination
Communicate documentation requirements to project stakeholders including:
EPC firms
Vendors
Construction teams
Procurement teams
CQV providers
Automation teams
Maintenance and Operations teams
Manage information exchange between client organizations and engineering design partners.
Work closely with project leadership and C&Q teams to ensure documentation requirements are met.
Compliance & Quality Assurance
Establish and execute auditing programs to verify document control processesmeetquality and compliance requirements.
Ensure documentation collection activities meet project timelines,regulatoryexpectationsand GMP compliance.
Maintain alignment with GMP and life sciences industry documentation standards.
Support qualification and validation activities through proper documentation control and traceability.
Leadership & Team Development
Ensure contract personnel and project teams areproperly trainedondocument and data management processes.
Provide leadership and guidance to project document control teams.
Support development of best practices and standardized document management processes across projects.
Mentor team members on documentation management tools, processes, and regulatory expectations.
Project Closeout & Lifecycle Support
Ensure all project documentation is complete, organized, and properlytransferredto Ownerproject closeout.
Manage final projectdocumentationdeliverables and turnover packages.
Support long-termlife-cycledocumentation requirements for facilities and assets.
Complete project information management closeout documentation.
Operational Performance & Delivery
Support successful project delivery through effective management of documentation and project information.
Ensure documentation processes support project timelines and quality standards.
Collaborate with project leadership to resolve documentation-related issuesimpactingproject delivery.
Experience Required
Bachelor’s Degree in Engineering, Life Sciences, Information Management, or related discipline (or equivalent experience).
Experience supporting capital projects, CQV, or GMP-regulated environments.
Experience managing project documentation systems and document control processes.
Experience working with engineering documentation, project drawings, and technical data.
Demonstrated ability to coordinate documentation across multiple project stakeholders.
Other Preferred
Ability to manage complex documentation across multiple projects and teams.
Strong organizational, communication, and stakeholder management skills.
Experience working in pharmaceutical, biotechnology, or life sciences environments preferred.
Ability to support projects across multiple client sites.
Applicants must be authorized to work in the United States on a full-time basis. We will not sponsor applicants for current or future work visas for this position. This position may require significant travel to support project and business needs. We cannot employ anyone with an invalid driver's license.
The annual compensation range for this full-time position is $(110,000 - $160,000). The final base pay offered to the successful candidate will be determined by factors including internal equity, work location, as well as individual qualifications, such as job-related skills, experience, and relevant education or training.
Skills
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