Use Your Power for Purpose

Every day, Pfizer’s unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients.

What You Will Achieve

In this role, you will:

Issuance, Retrieval, Archival and Control of GMP Documents/Records and DSMs (GMP documents) through Manual and Electronic systems.Issuance, Retrieval, Archival of DocumentsUp-keeping of Active Record CentersShred Bin managementTo upload IA templates into CICREnsure compliance with Enterprise Records Retention Schedule (ERRS) maintained by the enterprise records and Information Management (eRIM) group.Location mapping & tracking of documents/ records archived in document storage roomsEnsure documents/ records & DSM are accessible/ disposal due for retention.Verification of meta data and scanned images of document/ records and mapping of documents/records to Documents/ records management application/ Share path.Implement documentation systems, propose change control processes, and coordinate the review of procedures and forms.Execute tasks supporting Quality Systems functions and oversee Documentation Control and administrative functions of the DMS repository.

Here Is What You Need (Minimum Requirements):

Bachelor's/ master’s degree with 1 to 2 Years of Experience Diploma with 5+ Years of ExperienceKnowledge in Document Management and ControlEffective communication 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.

Quality Assurance and Control