Pfizer
Pharmaceutical
AssociateManager-ProcessEngineer
Neural analysis suggests this role is
optimal for Mid candidates.
“Associate Manager - Process Engineer at Pfizer. Skills: design, implementation, optimization, and validation of manufacturing processes and facilities, Process automation, Technology transfer, CIP/SIP design, Equipment and Facility engineering activities, CQV (Commissioning, Qualification, Validation), DCS & Automation - Recipe Development. Responsible for design, implementation, optimization, and validation of manufacturing processes and facilities in compliance with cGMP, regulatory, and safet”
What You'll Achieve.
deliver breakthroughs that change patients’ lives; accelerate and deliver best-in-class medicines to patients globally; make a global impact on patient health; ensure robust, compliant, and efficient operations
Industry & Context.
What They're Looking For.
Must Have
B- Tech / M -Tech with at Minimum 6 years of experience in Pharmaceutical Industry, Experience in handling the Green Field & Brown field Projects, Experience with working in MSAT / R&D / Process Engineering, Working knowledge of applicable industry test standards, relevant regulatory guidance, Design Controls, and the Product Development Process
Nice to Have
Hands on experience in DCS systems preferably DELTA V, Exceptional interpersonal skills and a proven track record of teamwork, Experience in working with DCS Logic developments, Testing and qualification activities, Effective verbal and written communication skills, Experience using common AI tools, including generative technologies
What You'll Do.
Responsible for design
and validation of manufacturing processes and facilities in compliance with cGMP
and safety requirements.
The role supports Process automation
Equipment and Facility engineering activities.
Drive the Continuous improvement initiatives to ensure robust
and efficient operations.
Participate in Design and engineering of new facilities and expansions.
Concept and basic design Layout developmental activities like (process flow
material/personnel flow) Capacity calculations and equipment design.
Execute and support CQV (Commissioning
Validation) activities for Equipment
Utilities and Automation systems.
Prepare and review: DQ / IQ / OQ / PQ protocols and reports.
Support regulatory audits and inspections related to qualified systems.
DCS & Automation - Recipe Development.
and maintain DCS batch recipes in line with process requirements and ISA‑88 standards.
Define process phases
and control strategies.
How You'll Work.
Team & Collaboration
proven track record of teamwork
Communication Scope
Effective verbal and written communication skills
Process & Methodology
Green Field & Brown field Projects
Full Job Description
**Use Your Power for Purpose** At Pfizer, our purpose is to deliver breakthroughs that change patients’ lives. Your work will leverage cutting-edge design and process development capabilities to accelerate and deliver best-in-class medicines to patients globally. Whether you are involved in discovery sciences, ensuring drug safety and efficacy, or supporting clinical trials, your contributions will be vital in helping Pfizer achieve new milestones and make a global impact on patient health. **What You Will Achieve** In this role, you will: * Responsible for **design, implementation, optimization, and validation of manufacturing processes and facilities** in compliance with **cGMP, regulatory, and safety requirements**. * The role supports **Process automation, Technology transfer, CIP/SIP design, Equipment and Facility engineering activities**. * Drive the Continuous improvement initiatives to ensure robust, compliant, and efficient operations. * Participate in **Design and engineering of new facilities and expansions**. * Concept and basic design Layout developmental activities like (process flow, utilities, material/personnel flow) Capacity calculations and equipment design. * Execute and support **CQV (Commissioning, Qualification, Validation)** activities for Equipment, Utilities and Automation systems. * Prepare and review: DQ / IQ / OQ / PQ protocols and reports. * Support regulatory audits and inspections related to qualified systems. * DCS & Automation - Recipe Development. * Develop, configure, test, and maintain **DCS batch recipes** in line with process requirements and ISA‑88 standards. * Define process phases, operations, interlocks, alarms, and control strategies. **Here Is What You Need** (Minimum Requirements) * B- Tech / M -Tech with at Minimum 6 years of experience in Pharmaceutical Industry. * Experience in handling the Green Field & Brown field Projects. * Experience with working in MSAT / R&D / Process Engineering . * Working knowledge of applic
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