Associate Compliance

Pfizer; India; On-site; INR 700,000 - 1,000,000; Full time

Job summary

Pfizer is seeking a candidate to join the Manufacturing Compliance team to manage document workflows and drive digital transformation of forms into electronic systems. You will support audits, coordinate cross-functional CAPA/CCF actions, and push process improvements in a fast-paced pharmaceutical setting.

The role emphasizes collaboration with CFTs, attention to detail, and ongoing project involvement to ensure readiness for inspections and compliance with cGMP standards.

Qualifications

• Masters or Bachelors degree in Science.
• More than 4+ years of experience in pharmaceuticals industry with knowledge of cGMP.
• Demonstrates skills in collaboration with cross-functional teams and attention to detail to achieve targets.

Responsibilities

• Be a member of the manufacturing compliance team and manage documents.
• Contribute to projects or handle small projects independently related to document management.
• Support during audits and assist in responding to audit observations.
• Initiate and coordinate CCF with cross-functional teams and drive closure.
• Track milestones of CAPA/CCF actions until closure.
• Perform walkthroughs in manufacturing areas and propose process improvements.

Skills

Attention to detail

Team collaboration

Document management

Audit support

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 .

Quality Assurance and Control