gcs Business process support specialistPfizer

ROLE SUMMARY
Provide business process support for Global Clinical Supply operations on projects relating to business process enhancement/modeling, 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.
ROLE 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/modeling
Portfolio and System 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
QUALIFICATIONS
A minimum of a BA or BS is required, advanced degree in relevant field desirable. Degree or professional certification in process design or change management, or equivalent experience.
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 Pfizer Human Performance tools
PHYSICAL/MENTAL REQUIREMENTS
Office work only
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Travel may require up to 15% for this role
May include domestic and international travel to GCS sites
May periodically require working US or EU hours to conduct / lead - meetings
#LI-PFE
Work Location Assignment: On Premise
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
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Pfizer

Makati City, Metro Manila
Permanent
Full-time