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The Role
The International Associate supports Labeling Managers by maintaining documentation, managing workflows, providing technical support, proof-reading labeling texts, and ensuring data integrity and quality checks in compliance with SOPs.
Summary Generated by Built In
JOB SUMMARY
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.
JOB RESPONSIBILITIES
QUALIFICATIONS / SKILLS
SKILLS
QUALIFICATIONS
EXPERIENCE
Required Experience
Preferred Experience
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Important Notice for Applicants
At Pfizer, we value your privacy and security. Please note:
We never request payment, bank details, or confidential personal information during the recruitment process.
If you receive suspicious messages or job offers outside these channels, please report them immediately to [[email protected]]
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Regulatory Affairs
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.
JOB 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
- Preferred - Life sciences, pharmacy graduate or equivalent; or equivalent relevant professional experience.
EXPERIENCE
Required 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.
Preferred Experience
- '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.
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Important Notice for Applicants
At Pfizer, we value your privacy and security. Please note:
- All job applications must be submitted only through our official channels:
- Pfizer Careers Website: Careers | Pfizer
- Verified LinkedIn page: https://www.linkedin.com/
- Verified local job board - Pharma360: Công ty dược tuyển dụng dược sĩ đại học - Việc làm dược sĩ Pharma360
We never request payment, bank details, or confidential personal information during the recruitment process.
If you receive suspicious messages or job offers outside these channels, please report them immediately to [[email protected]]
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Regulatory Affairs
Top Skills
Gdms
Ms Access
Excel
Ms Sharepoint
Pfleet
What the Team is Saying
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The Company
What We Do
Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.
Why Work With Us
We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.
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Employees engage in a combination of remote and on-site work.
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