LOM - International Associate (Labeling)

<p><b>JOB SUMMARY</b></p><p><span>The LOM - International Associate is responsible for supporting Labeling Managers by maintaining documentation in labeling systems so that SOP requirements are fulfilled. Maintenance of workflow management tools and mailboxes and associated technical support are also an essential part of the role.</span></p><p></p><p><b>JOB RESPONSIBILITIES </b></p><ul><li>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.</li><li>Ad hoc support for labeling deliverables.</li><li>Proof-reading of labeling text.</li><li>System data integrity and quality checks.</li></ul><p></p><p><b>QUALIFICATIONS / SKILLS</b></p><p><u><b>SKILLS</b></u></p><ul><li>Knowledge of the principles and concepts of labeling.</li><li>Knowledge of key regulatory and labeling principles and local regulations</li><li>Proficient in use of systems consistent with business expectations, and understands importance of systems in maintaining high compliance figures</li><li>Fluency in English language important however multi-language skills are advantageous</li><li>Clear and effective written and verbal communications</li><li>Understanding of the importance of Standard Operating Procedures (SOPs), systems and processes in underpinning quality and compliance of deliverables</li><li>Experience working with structured data, such as in enterprise databases, MS Excel, MS SharePoint and/or MS Access</li></ul><p></p><p><u><b>QUALIFICATIONS</b></u></p><ul><li>Preferred - Life sciences, pharmacy graduate or equivalent; or equivalent relevant professional experience.</li></ul><p></p><p><u><b>EXPERIENCE</b></u></p><p><u>Required Experience</u></p><ul><li>Demonstrated ability to develop strong and positive working relationships across multiple cultures and locations.</li><li>Demonstration of attention to detail and problem-solving skills.</li><li>Proven technical aptitude and ability to quickly learn new software, regulations and standards.</li></ul><p><u>Preferred Experience</u></p><ul><li>‘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.</li></ul><p></p><p>-----</p><p><b>Important Notice for Applicants</b><br />At Pfizer, we value your privacy and security. Please note:</p><ul><li><p>All job applications must be submitted <b>only through our official channels</b>:</p></li><li><p>Pfizer Careers Website: <a href="https://www.pfizer.com/about/careers" target="_blank">Careers | Pfizer</a></p></li><li><p>Verified LinkedIn page: <a href="https://www.linkedin.com/" target="_blank">https://www.linkedin.com/</a></p></li><li><p>Verified local job board - Pharma360: <a href="https://pharma360.vn/viec-lam/" target="_blank">Công ty dược tuyển dụng dược sĩ đại học - Việc làm dược sĩ Pharma360</a></p></li></ul><p></p><p>We <b>never request payment, bank details, or confidential personal information</b> during the recruitment process.</p><p></p><p>If you receive suspicious messages or job offers outside these channels, please report them immediately to <b>[ProtectPfizer&#64;pfizer.com]</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Regulatory Affairs<p></p><p></p>