Associate Manager - Automation

By Admin · IT & Software in Life Sciences

VISAKHAPATNAM (IN)ONSITEPOSTED: 10/4/2026
PHARMAFull time
HIRING ORGANIZATIONPFIZERBiopharmaceutical / Healthcare
Pfizer

ROLE OVERVIEW

Pfizer’s Vizag manufacturing site plays a critical role in producing essential medicines for global markets. As Associate Manager – Automation, you will be the technical owner of process control systems—DeltaV DCS, SCADA, and PLCs—that keep production lines reliable, compliant, and efficient. This role sits at the intersection of engineering, validation, and regulatory compliance, ensuring automation systems meet 21 CFR Part 11, cGAMP, and GMP expectations. You will support investigations, audits, periodic reviews, and capital projects, directly impacting Pfizer’s ability to deliver medicines without interruption. For experienced automation engineers seeking a purpose-driven career, this position offers deep exposure to pharmaceutical manufacturing, cross-functional collaboration, and the chance to shape site automation standards. It is an ideal move for professionals who want to combine hands-on technical work with meaningful patient impact.

ROLE DEFINITION & RESPONSIBILITIES

  • •Operate, troubleshoot, and maintain DeltaV DCS, SCADA, and PLC-based manufacturing control systems to ensure uninterrupted production and data integrity.
  • •Lead periodic reviews, risk assessments, and change controls for automated systems in alignment with validation and regulatory requirements.
  • •Author and review user requirement specifications, functional/design specifications, and vendor automation documentation, including traceability matrices.
  • •Support FAT, commissioning, qualification, and execution of qualification protocols for new and modified automated control systems.
  • •Serve as System Admin for site control systems and data historian, managing user access, backups, archiving, and restoration of automation configurations.
  • •Maintain manufacturing, control, and process I/O networks; troubleshoot industrial communication hardware and software issues.
  • •Provide on-the-floor automation support, train operations/validation/maintenance teams, and support audits and investigations as automation subject matter expert.
  • •Drive compliance initiatives around 21 CFR Part 11, cGAMP, system security, and site automation standards for hardware and software.

QUALIFICATIONS & REQUIREMENTS

REQUIRED QUALIFICATIONS

  • Bachelor of Technology or Engineering in Electronics, Instrumentation, or an equivalent engineering discipline.
  • 8–12 years of combined experience in process control, automation, PLC, SCADA, and DCS within pharmaceuticals, biotechnology, or life sciences.
  • Proven ability to read and interpret electrical control system diagrams, including panel wiring, loop drawings, and layout schedules.
  • Hands-on experience walking down control system diagrams and red-lining them to reflect as-built conditions.
  • Solid technical knowledge of field instrumentation, industrial communication networks, and related hardware/software.
  • Basic understanding of SQL servers and databases used in manufacturing automation environments.
  • Familiarity with FDA, ISO, EU, and ICH guidelines relevant to automated and computerised systems.

PREFERRED QUALIFICATIONS

  • •Pharmaceutical manufacturing experience
  • •Programming proficiency (e.g., Python, VBA, or PLC languages)
  • •AI tools for problem solving (ChatGPT, Microsoft Copilot)
  • •Good Manufacturing Practices (GMP)
  • •Training and mentoring ability

REQUIRED VERIFIED SKILLS

DeltaV DCS
SCADA & PLC Programming
21 CFR Part 11 Compliance
cGAMP & GMP Validation
Automation System Administration
Industrial Communication Networks
Control System Troubleshooting
User Requirement Specification (URS)
Risk Assessment & Change Control
Data Historian Management

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting

ORGANIZATION CONTEXT & CULTURE

Pfizer Inc. is an American multinational pharmaceutical and biotechnology corporation. It is dedicated to the discovery, development, manufacturing, marketing, and sale of medicines and vaccines worldwide. The company focuses on breakthrough science to deliver innovative treatments across various therapeutic areas to improve health outcomes.

TEAM SIZE: 80,000+ employees
INDUSTRY: Biopharmaceutical / Healthcare

EXPECTED CAREER ROADMAP

From this role, you can progress to Senior Manager – Automation, Site Automation Lead, or Engineering Director within Pfizer’s global supply network. The exposure to capital projects, regulatory audits, and cross-site standards makes you competitive for roles in MSAT, validation, or technical operations. In 2–5 years, you could move into global engineering, digital manufacturing, or smart factory initiatives. Alternatively, you can pivot to automation consulting, pharmaceutical equipment vendors, or CRO/CDMO engineering functions. The combination of GMP compliance and hands-on control systems expertise is highly transferable across India’s growing biopharma and vaccine manufacturing sector. Many professionals also transition into quality assurance or regulatory affairs focused on computerised system validation.

APPLICATION ADVISORY

Tailor your resume to highlight DeltaV, SCADA, and PLC project details, including system sizes, validation deliverables, and audit outcomes. Prepare examples of troubleshooting, change controls, and 21 CFR Part 11 compliance. Interviewers will probe your understanding of URS, FS, HDS, and traceability matrices, plus your ability to red-line electrical diagrams. Brush up on GMP, data integrity, and industrial networks. Be ready to discuss how you train others and use AI responsibly. Emphasise safety, reliability, and patient impact in every answer.

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