JOB RESPONSIBILITIES

• Contributes to the completion of moderately complex projects under the direction of more senior labeling managers.

• Utilizes regulatory knowledge to produce non-complex LPDs, LLDs and PLDs where there are unambiguous relationships to source documents and clear local regulatory principles to follow, requesting advice or input from other functions when appropriate.

• Produces other labeling-related documentation for submission to HAs such as track change versions, annotated labels, comparison tables and annotated supporting documentation.

• Performs QC check of other colleagues’ work.

• 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.

SKILLS

• Basic knowledge/understanding of the principles and concepts of labeling.

• Knowledge of key regulatory and labeling principles and local regulations.

• 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.

• Clear and effective written and verbal communications.

• Understanding of the importance of SOPs, systems and processes in underpinning quality and compliance of deliverables.

• Experience working with structured data, such as in enterprise databases, MS Excel, MS SharePoint and/or MS Access.

QUALIFICATIONS

• Life sciences, pharmacy graduate or equivalent; or equivalent relevant professional experience.

EXPERIENCE

• Demonstrated ability to develop strong and positive working relationships across multiple cultures and locations. (Preferred)

• Demonstration of attention to detail and problem-solving skills.

• Proven technical aptitude and ability to quickly learn new software.

• Proven technical aptitude and ability to quickly learn regulations and standards.

• ‘Hands on’ registration experience associated with development, maintenance and commercialization activities within Regulatory Affairs; preferably from the perspective of a Country office or Regional Regulatory Strategy important and advantageous especially with the perspective of the implications of a Core Data Sheet on LPDs.

• Ability to understand, assess and manage the regulatory implications of product strategy with regard to the product label

• Knowledge of global/regional regulatory guidelines and requirements in addition to knowledge of Clinical Variations is important.

• 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. (Preferred)

• Demonstrated project management, attention to detail and problem-solving skills. (Preferred)

• Proven strength in logical, analytical and writing ability essential

  
Work Location Assignment: Hybrid

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

Regulatory Affairs