global clinical supply Business process support specialistPfizer
Workplace: MetroManila, Manila, Makati
Salary: Agreement
Work form: Full time
Posting Date: 09/11/2025
Deadline: 23/12/2020
Role Summary:
Provide business process support for Global Clinical Supply operations on projects relating to business process enhancement,
quality compliance monitoring, quality investigations, program/protocol management and continuous improvement in the context of procedural documentation development and redesign (policies, standards, standard operating procedures (SOPs)), communications, training development, monitoring, data analysis and development and other relevant supporting tools and documentation.
Responsibilities:
SOP and Process Support
Work in collaboration with subject matter experts in the development, revision, process mapping, implementation and maintenance of procedural (policies, standard operating
procedures and supporting documents) and training documentation related to Global Clinical Supply
Facilitate procedure redesign and related development and provision of training documents in accordance to established plan while engaging relevant SMEs and stakeholders
Evaluate procedural documentation against evolving industry/regulatory requirements and expectations, audit/inspection findings, business needs, changes in industry standards and client feedback and trends, including making recommendations for changes when necessary
Manage queries and deviations from the organization related to assigned policies/SOPs, and support SOP revisions/reformatting
Quality Systems Support
Support the review and trending of relevant Quality Events (SQE/QTS) to identify potential risk indicators and mitigations
Work across GCS functional lines and QA to coordinate investigation documentation in quality system. Monitor investigation record progress driving to due date and escalating when appropriate.
Support inspection readiness activities through data assembly, as directed
Portfolio and Systems Support
Provide enhanced system support for reporting (i.e. Spotfire, CT-FAST, etc.) Including Spotfire (visualization support, maintenance and development) and SharePoint (support, maintenance and development)
Support Blind Review Board (BRB) efforts to streamline data, such as developing a single-entry point that serves as BRB discussion substrate, TPB tool and knowledge management repository
Monitor large and/or complex programs/protocols and initiate all system and/or documentation to enable clinical supply processes to maintain clinical supply at depot/site
Degree Requirements:
A minimum of a BA or BS in related field is required.
Required Experience/Skills:
2-5 years' experience in process design and documentation of pharmaceutical business processes
Training or experience in safety, regulatory, medical and/or clinical supply process training development, delivery and/or implementation
Ability to work in and/or facilitate multi-phase complex projects with multiple contributors/collaborators, facilitate cross functional teams, optimize subject matter involvement, and interact at all levels in a matrix environment
Strong organizational skills and ability to prioritize multiple projects and meet targeted deliverables and deadlines; strong planning and multi-tasking skills
Ability to adapt to changing situations and work well under pressure
Technical proficiency, including skills in use of common desktop tools (MS Word, MS Excel, MS Project, Visio); Office365 and SharePoint; tools for
process design and mapping; reporting (Spotfire); and systems for document management, publishing,
communication, and learning management
Understanding of the fundamentals of electronic publishing of procedural documents
Strong verbal and written communication skills
In-depth understanding of pharmaceutical business processes and regulations, guidelines and industry standards for compliance
Proficient and trained in using root cause analysis tools to drive quality investigations to appropriate closure including remediations as required
Proficient and trained in using Human Performance tools, Pfizer tools preferred
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Research and Development
Pfizer
Provide business process support for Global Clinical Supply operations on projects relating to business process enhancement,
quality compliance monitoring, quality investigations, program/protocol management and continuous improvement in the context of procedural documentation development and redesign (policies, standards, standard operating procedures (SOPs)), communications, training development, monitoring, data analysis and development and other relevant supporting tools and documentation.
Responsibilities:
SOP and Process Support
Work in collaboration with subject matter experts in the development, revision, process mapping, implementation and maintenance of procedural (policies, standard operating
procedures and supporting documents) and training documentation related to Global Clinical Supply
Facilitate procedure redesign and related development and provision of training documents in accordance to established plan while engaging relevant SMEs and stakeholders
Evaluate procedural documentation against evolving industry/regulatory requirements and expectations, audit/inspection findings, business needs, changes in industry standards and client feedback and trends, including making recommendations for changes when necessary
Manage queries and deviations from the organization related to assigned policies/SOPs, and support SOP revisions/reformatting
Quality Systems Support
Support the review and trending of relevant Quality Events (SQE/QTS) to identify potential risk indicators and mitigations
Work across GCS functional lines and QA to coordinate investigation documentation in quality system. Monitor investigation record progress driving to due date and escalating when appropriate.
Support inspection readiness activities through data assembly, as directed
Portfolio and Systems Support
Provide enhanced system support for reporting (i.e. Spotfire, CT-FAST, etc.) Including Spotfire (visualization support, maintenance and development) and SharePoint (support, maintenance and development)
Support Blind Review Board (BRB) efforts to streamline data, such as developing a single-entry point that serves as BRB discussion substrate, TPB tool and knowledge management repository
Monitor large and/or complex programs/protocols and initiate all system and/or documentation to enable clinical supply processes to maintain clinical supply at depot/site
Degree Requirements:
A minimum of a BA or BS in related field is required.
Required Experience/Skills:
2-5 years' experience in process design and documentation of pharmaceutical business processes
Training or experience in safety, regulatory, medical and/or clinical supply process training development, delivery and/or implementation
Ability to work in and/or facilitate multi-phase complex projects with multiple contributors/collaborators, facilitate cross functional teams, optimize subject matter involvement, and interact at all levels in a matrix environment
Strong organizational skills and ability to prioritize multiple projects and meet targeted deliverables and deadlines; strong planning and multi-tasking skills
Ability to adapt to changing situations and work well under pressure
Technical proficiency, including skills in use of common desktop tools (MS Word, MS Excel, MS Project, Visio); Office365 and SharePoint; tools for
process design and mapping; reporting (Spotfire); and systems for document management, publishing,
communication, and learning management
Understanding of the fundamentals of electronic publishing of procedural documents
Strong verbal and written communication skills
In-depth understanding of pharmaceutical business processes and regulations, guidelines and industry standards for compliance
Proficient and trained in using root cause analysis tools to drive quality investigations to appropriate closure including remediations as required
Proficient and trained in using Human Performance tools, Pfizer tools preferred
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Research and Development
Pfizer
Other Info
Makati City, Metro Manila
Permanent
Full-time
Permanent
Full-time
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Pfizer
About the company
Position global clinical supply Business process support specialist recruited by the company Pfizer at MetroManila, Manila, Makati, Joboko automatically collects the salary of , finds more jobs on Global Clinical Supply Business Process Support Specialist or Pfizer company in the links above