Associate Compliance

Pfizer; Visakhapatnam; On-site; INR 600,000 - 900,000; Full time

Job summary

Pfizer in Visakhapatnam seeks a Document Management professional to join the manufacturing compliance team. You will manage documents, drive electronic transformation of forms, and support audits to ensure readiness for inspections.

The role requires 4+ years in pharma, cGMP knowledge, and strong cross-functional collaboration with attention to detail to meet targets and quality standards.

Qualifications

• Masters or Bachelors degree in Science.
• 4+ years of experience in pharmaceuticals industry and knowledge of cGMP.
• Strong collaboration with cross-functional teams and attention to detail.

Responsibilities

• Digitize forms and convert manual records into an electronic system via SDS.
• Maintain document management including issuance and retrieval of documents.
• Support responses to audit observations.
• Initiate CCF, coordinate with CFTs for impact assessment, obtain pre-approval, implement and close.
• Track milestones for CAPA/CCFs through to closure.
• Perform walkthroughs in manufacturing areas and suggest process improvements.

Skills

Collaboration with CFTs

Attention to detail

Education

Masters or Bachelors in Science

Tools

PDOCS

SDS

SAP

Job description

Use Your Power for Purpose

Our core principle and commitment towards the patients “Patients lives depends on us” is based on the innovative, quality and compliance. The role you play directly have impact on the patients.

What you will achieve:

You will be member of manufacturing compliance team and will be responsible for Document management.

You will get a chance to be part of the projects or handle the small projects independently associated with the document management.

It is your hard work and consistent performance that will make Pfizer proud to achieve new targets, help patients and readiness for on-time inspections.

How will you achieve it:

• Digital Transformation or conversion of manual FORMS into electronic system through SDS.


• Maintaining the document management (Issuance & retrieval of documents).


• Support during the preparation of response to audit observations.


• Responsible for the CCF initiation, coordination with CFTs for impact assessment and CCF pre-approval, implementation and closure.


• Track and monitor the detailed milestones of the actions (CAPA/ CCFs) till closure of the actions.


• Responsible to perform the walkthrough in the manufacturing area and propose the process improvement actions.

Qualifications:

Must Have

• Masters or Bachelors degree in Science.


• More than 4+ years of experience in pharmaceuticals industry Knowledge of Good manufacturing practices (cGMP).


• Demonstrates skills in collaboration with CFTs & paying attention to the details to achieve the target

Nice to have:

• Technical knowledge of Software like PDOCS, SDS & SAP system.


• Experience in Pharmaceuticals manufacturing

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.