Digital Labeling - Associate (DLM Associate)

Use Your Power for Purpose
As DLM-Associate in Labeling Operations at Pfizer, you will play a crucial role directly contributing to the improvement of patients' lives. Your work will ensure that our products are accurately labeled, meeting regulatory requirements and providing essential information to healthcare professionals and patients. This role offers a unique opportunity to make a tangible impact on global health while working with a team of dedicated professionals.
What You Will Achieve
In this role, you will:

• Be responsible for supporting Labeling Managers by maintaining documentation in labeling systems so that SOP requirements are fulfilled
• Help maintain workflow management tools and mailboxes and provide associated support

RESPONSIBILITIES

• Supports Labeling Managers by maintaining documentation in GDMS, PfLEET and other systems so that SOP requirements are fulfilled
• Maintenance of workflow management tools and mailboxes
• Ad hoc support for labeling deliverables
• Proof-reading of labeling text
• System data integrity and quality checks

QUALIFICATIONS / SKILLS
SKILLS

• Knowledge 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 Standard Operating Procedures (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 - Preferred
EXPERIENCE

• 1-5 yrs relevant experience
• Demonstrated ability to develop strong and positive working relationships across multiple cultures and locations
• Demonstration of attention to detail and problem-solving skills
• Proven technical aptitude and ability to quickly learn new software, regulations and standards
• '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- Preferred

ORGANIZATIONAL RELATIONSHIPS

• Reporting relationship to GILA Head Labeling Operations, International Labeling Lead, Partners with Pfizer Global Regulatory groups and other platform lines as required
• Supports Global Regulatory and Labeling Operations initiatives as required

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