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Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
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Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
In this role, you will process Individual Case Safety Reports, assess case validity, and ensure compliance with drug safety regulations.
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Use Your Power for Purpose
As an 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 provide operational support for Global Labeling which includes;
Here Is What You Need (Minimum Requirements)
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
- Basic understanding of regulatory requirements for labeling
- Excellent written and verbal communication skills
- Ability to work independently and as part of a team
- Ability to manage multiple tasks simultaneously
- Basic project management skills
Bonus Points If You Have (Preferred Requirements):
- Knowledge of global labeling regulations
- Strong interpersonal skills
- Strong analytical skills
- Ability to interpret and apply regulatory guidelines
- Effective problem-solving skills
Work Location Assignment: On Premise
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Regulatory Affairs
As an 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 provide operational support for Global Labeling which includes;
- Generate necessary renditions in GDMS (e.g., clean and marked PDF, clean and marked MS Word) and bookmark renditions as appropriate.
- Facilitate workflow through corporate document repository, e.g., GDMS.
- Finalize documents post QC (including update of GDMS document properties such as entry of PfLEET2 number, update of document title, update CDS cover page etc.).
- Manage the document status in GDMS and notify internal stakeholders of the availability of labeling documents.
- Create/Update SPL for USPIs, check and upload to GDMS upon receipt, notify internal stakeholders of its availability (e.g., Regulatory, Drug Listing).
- Responsible for ensuring compliance to Company's submission standards, policies and procedures. Ensure all actions taken within role follow applicable SOPs and associated documents so that high quality delivery of outputs and compliance is maintained.
Here Is What You Need (Minimum Requirements)
- Bachelor's degree required preferably in a science / life sciences related degree.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
- Basic understanding of regulatory requirements for labeling
- Excellent written and verbal communication skills
- Ability to work independently and as part of a team
- Ability to manage multiple tasks simultaneously
- Basic project management skills
Bonus Points If You Have (Preferred Requirements):
- Knowledge of global labeling regulations
- Strong interpersonal skills
- Strong analytical skills
- Ability to interpret and apply regulatory guidelines
- Effective problem-solving skills
Work Location Assignment: On Premise
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Regulatory Affairs
Pfizer Chennai, Tamil Nadu, IND Office
Chennai, India
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