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We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
Supports pharmaceutical manufacturing compliance through document management, electronic form conversion, audit response preparation, change control coordination, CAPA and CCF tracking, manufacturing walkthroughs, and process improvement. The role collaborates with cross-functional teams to ensure documentation readiness and timely inspection preparation while maintaining compliance with cGMP requirements.
Summary Generated by Built In
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
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
Skills Required
- Bachelor’s or master’s degree in Science
- More than 4 years of experience in the pharmaceutical industry
- Knowledge of current Good Manufacturing Practices (cGMP)
- Collaboration skills with cross-functional teams
- Strong attention to detail
- Technical knowledge of PDOCS, SDS, and SAP
- Experience in pharmaceutical manufacturing
What the Team is Saying
Daniel
Diagnostics Launch Lead
Anna
R&D Privacy Steward
Esteban
Specialist
Pfizer
Pfizer Compensation & Benefits Highlights
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Healthcare Strength — Health coverage is described as comprehensive, spanning medical, dental, vision, and robust mental‑health benefits, with eligible Pfizer medications available at no cost in U.S. plans. Family‑building support and transgender‑inclusive care are explicitly included, alongside wellbeing resources such as a reimbursement wallet and telehealth options.
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Retirement Support — Retirement programs feature a 401(k) with company matching plus an additional Retirement Savings Contribution, complemented by company‑subsidized life, short‑term disability, and long‑term disability insurance. Materials also reference subsidized retiree medical coverage for eligible groups.
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Leave & Time Off Breadth — Paid vacation, holidays, personal days, and paid parental and caregiver leave are consistently highlighted in current U.S. summaries and job postings. Options like buying extra vacation days and transition‑back support strengthen the time‑off offering.
Pfizer Insights
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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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Pfizer Offices
Hybrid Workspace
Employees engage in a combination of remote and on-site work.
Typical time on-site:
2.5 days a week
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