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Hub Labeling Manager (HLM), Manager

Pfizer


Location:
Augusta, GA 30901
Date:
02/02/2018
2018-02-022018-03-05
Pfizer
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Job Details

**Job summary**



The Hub Labeling Manager (HLM), Manager level, is responsible for executing the content management of Local Product Documents (LPDs), Local Label Documents (LLDs) and Patient Leaflets for nationally registered products for their assigned products across multiple countries/regions. The full range of labeling documentation may be produced.







Responsibilities







+ Utilize regulatory expertise to review, develop and deliver labeling documents such as the LPD, LLD and Patient Leaflet to support submissions to the Regulatory Authorities across regions, requesting advice or input from other functions when appropriate.



+ Production of other labeling-related documentation for submission to HAs such as track change versions, annotated labels, comparison tables and annotated supportive documentation.



+ The full range of labeling documentation may be produced, including labels for NCEs or Product Extensions, as well as other complex revisions.



+ For deliverables in scope, support responses to inquiries from Pfizer colleagues in response to inspection activities and may provide support during regulatory agency questions.



+ May coordinate labeling revisions when there is a regional, global or therapeutic area impact across multiple countries



+ May mentor or train more junior labeling managers in their day-to-day activities



+ Ability to run training and awareness sessions on labeling processes and ability to clearly articulate expectations of the labeling process to stakeholders.



+ Takes appropriate risks to advance new concepts and methodologies that are moderately complex, participating in pilots as directed and other continuous improvement projects.



+ Identifies incremental improvements to labeling-related processes and systems for exploration by more senior labeling managers.



+ Meets defined targets on productivity, quality and compliance, as set by and overseen by management.



+ Meets strategic targets for labeling deliverables as defined for the function, and communicates progress against these targets or issues which affect these targets, and proposes remediation







**Technical Skill Requirements**







+ Has thorough knowledge of the principles, concepts and theories of labeling, and awareness of principles and concepts of other labeling-related disciplines.







+ Understands and applies labeling regulation knowledge in the region and in assigned local countries, and is able to interpret impact of that regulation on development of labeling text.







+ Proficient in use of systems consistent with business expectations, and understands importance of systems in maintaining high compliance figures







+ Fluency in English language important however multi-language skills are advantageous



+ Written and verbal communications clear and effective



+ Understands and applies labeling regulation in the region and in assigned local countries, and is able to interpret impact of that regulation on development of labeling text



+ Understanding of the importance of Standard Operating Procedures (SOPs), systems and processes in underpinning quality and compliance of deliverables







**Education and Experience**







+ Life sciences, pharmacy graduate or equivalent



+ Advanced academic qualifications/degree such as PhD an advantage but not essential



+ Significant 'Hands on' registration experience associated with development, maintenance and commercialization activities within Regulatory Affairs (Human Medicinal Products); preferably from the perspective of a Country office or Regional Regulatory Strategy important and advantageous especially with the perspective of the implications of a CDS on LPDs



+ Proven ability to successfully understand regulatory implications of product strategy with regard to the produce label, assessment and practical management of associated impacts.



+ Demonstrated ability to interpret and apply regional/local regulatory guidance around labeling and associated supportive documentation, both in the pre-approval and post approval (maintenance) stages



+ Demonstrated ability to develop strong and positive working relationships across multiple cultures and locations.



+ Knowledge of global/regional regulatory guidelines and requirements important



+ Knowledge of Clinical Variations preferred



+ Proven strength in logical, analytical and writing ability essential



+ Readability Testing knowledge an advantage but not essential



+ Demonstrated project management, attention to detail and problem solving skills required.







All applicants must have the relevant authorisation to live and work in the UK.



The closing deadline for applications is February 15th.



Day (standard) (United Kingdom)



Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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