Associate Manager - MSAT

Posted Yesterday
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Vizag, Vishākhapatnam, Andhra Pradesh, IND
In-Office
Expert/Leader
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
Supports pharmaceutical manufacturing technology operations through DeltaV DCS configuration, batch recipe and control logic development, PI Historian integration, and system qualification. Creates DQ, IQ, OQ, and PQ documentation, maintains traceability and audit readiness, and ensures compliance with 21 CFR Part 11, GAMP 5, CSV, data integrity, and validation standards. Requires expertise in batch control, Historian architecture, industrial protocols, system integration, and regulated-industry automation.
Summary Generated by Built In
Use Your Power for Purpose
As a Process Engineer , you will be part of Tech Operations team and play a crucial role in improving patients' lives while working at Pfizer. Your contributions will directly impact the development and delivery of innovative solutions that enhance the quality of life for patients worldwide. Join us in our mission to bring breakthroughs that change patients' lives.
What You Will Achieve
In this role, you will work as Process Engineer with hands-on experience in Delta DCS systems, PI Historian to support the development and qualification of automation logic, Historian integrations in compliance with 21 CFR Part 11 and the latest validation standards.
The role involves supporting design documents and developing qualification protocols, as well as configuring recipes, formulas, and controlling logic in Delta V DCS system, Historian systems along with Qualifications.
Key Responsibilities:
  • Creation of DCS Recipe parameters, Formulas and developing process flows as per Tech transfer inputs.
  • Review and interpret Software Design Specifications (SDS), Functional Specifications (FS), and related documents to understand automation requirements.
  • Prepare comprehensive Qualification Documents including - Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ),Performance Qualification (PQ)
  • Ensure documentation aligns with 21 CFR Part 11, GAMP 5, and internal validation SOPs.
  • Develop and configure DeltaV DCS logic, including Batch Recipes, Control Modules, Equipment Modules, Formulas and Phases
  • Maintain traceability matrices and ensure audit readiness of all documentation.
  • Qualification of Historian systems.
  • Understanding batch recipes, formulas, and control strategies.
  • Solid understanding of 21 CFR Part 11, GAMP 5, and CSV principles.
  • Strong documentation and technical writing skills.
  • Familiarity with data integrity and audit trail requirements.
  • Knowledge of ISA-88 batch control standards. 
  • Knowledge of ALCOA Principles.
  • PI System Architecture Knowledge of PI Data Archive, Asset Framework (AF), Event Frames, and PI Vision.
  • Interface Configuration Experience with OPC, Modbus, and other industrial protocols
  • Data Modeling & Contextualization Building AF templates and event frames for batch and equipment tracking
  • System Integration Connecting PI with MES, ERP & SCADA systems
  • Reporting Tools Using PI Datalink, PI Vision, and PI Rt Reports for analytics and compliance reporting.

Here Is What You Need (Minimum Requirements)
  • Bachelor's degree in Electrical and Electronics, Automation, Chemical or related engineering discipline.
  • Minimum 10 years of experience in automation engineering within a regulated industry (pharma/biotech preferred).
  • Strong working knowledge of DeltaV DCS systems.
  • Expertise on 7016 - Delta Batch Implementation or equivalent hands-on experience.

Bonus Points If You Have (Preferred Requirements)
  • Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

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.
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 .
Engineering

Skills Required

  • Bachelor's degree in Electrical and Electronics, Automation, Chemical, or related engineering discipline
  • Minimum 10 years of automation engineering experience within a regulated industry, preferably pharma or biotech
  • Strong working knowledge of DeltaV DCS systems
  • Expertise in 7016 Delta Batch Implementation or equivalent hands-on experience
  • Experience using generative AI tools such as ChatGPT or Microsoft Copilot, with understanding of responsible AI practices

What the Team is Saying

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Pfizer

Pfizer Compensation & Benefits Highlights

  • 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.
  • 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.
  • 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.

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The Company
HQ: New York, NY
121,990 Employees
Year Founded: 1848

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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Employees engage in a combination of remote and on-site work.

Typical time on-site: 2.5 days a week
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