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[Full Time] Associate Manager - MQA at Pfizer

Thu, 19 Mar 2026 12:00:00 +0530

Job Description

Role Summary

The MQ TS Downstream Associate Manager is responsible for primary contact of quality on the floor, particularly in the Terminal sterilization, Visual Inspection and Packing areas of production and monitor processes for compliance to cGMP standards.

Responsibilities

Responsible for ensuring operating state of cGMP compliance in Terminal Sterilization, Visual Inspection and Packaging operations.

Maintain regulatory compliance in accordance with cGMP practices

Ensure manufacturing policies and procedures conform to Pfizer standards

Knowledge and hands on experience in reviewing eBR and assessing the impact of AMPs exceptions with technical support/inputs from Sr. Team leader.

Review of Batch reports, and Equipment audit trails

Perform Acceptable Quality level sampling, Inspection and record the results in Batch records for all products

Perform batch start-up and end activities viz. sensor challenge tests, recipe review etc.

Perform random process checks for Terminal Sterilization, Visual Inspection and Packaging

Perform Daily walkthroughs and report observations to the Sr. Team leader.

Perform Equipment breakdown assessments w. r. t to Product Quality and patient safety with technical support/inputs from Sr. Team Leader.

Review and assessment of equipment alarms and review of quarterly alarm trends.

Report any non-compliance to the Sr. Team Leader

Should have trouble shooting abilities in manufacturing area, which helps the organization to develop, implement and achieve its mission, vision and values.

Identify gaps and involve in Process and Procedure Simplification, thereby reduce downtime, and increase the Efficiency. AMPS Recipe review and validation of recipe.

Experience in handling regulatory, corporate and internal auditors/ inspectors

Here Is What You Need (Minimum Requirements)

Candidate must have B. Pharm, M. Pharm, MSc. with 6-8 years of experience in Manufacturing Quality Assurance / Quality Assurance / Production of a pharmaceutical manufacturing facility.

Bonus Points If You Have (Preferred Requirements)

Experience in quality administered systems
Strong organizational skills and attention to detail
Experience with regulatory compliance and documentation
Ability to mentor and review the work of other colleagues

Quality Assurance and Control

Job Classification

Industry: Pharmaceutical & Life Sciences
Functional Area / Department: Production, Manufacturing & Engineering
Role Category: Management
Role: Manufacturing Operations Manager
Employement Type: Full time

Contact Details:

Company: Pfizer
Location(s): Visakhapatnam

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[Full Time] Associate Manager SES (Upstream) at Pfizer

Fri, 13 Mar 2026 12:00:00 +0530

Job Description
Use Your Power for Purpose

At Pfizer, we believe that every role contributes to our mission of improving patients lives. Whether you are involved in the design and development of manufacturing processes for products or supporting the upkeep of systems, engineering is crucial to ensuring customers and patients receive the medicines they need. By collaborating with our forward-thinking engineering team, youll play a pivotal role in accelerating the delivery of medicines to the world.

What You Will Achieve

In this role, you will:

Oversee maintenance and reliability engineering tasks, including the redesign, upkeep, and repair of utility systems, buildings, and equipment.

Contribute to moderately complex projects, managing time effectively and developing short-term work plans.

Provide engineering support for developing scopes of work, project execution plans, and engineering studies for equipment installation or modification.

Offer operational support, review preventive and corrective work orders, and manage technical writing and document reviews.

Ensure calibration compliance with Current Good Manufacturing Practices, contemporary technologies, and best aseptic practices.

Participate in Root Cause Failure Analysis investigations and update equipment reliability plans, collaborating with Production and Quality Team Leads.

Promote workplace safety by following site safety procedures and performing proactive safety assessments.

Actively participate in site and corporate initiatives, and serve as a liaison between quality, operations, and regulatory/compliance for timely closure of investigations.

Here Is What You Need (Minimum Requirements)

High school diploma (or equivalent) with 8+ years of experience or associate s degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience

Experience with Root Cause Failure Analysis, Equipment Criticality Ranking, PM and/or Failure Modes and Effects Analysis

Experience with process automation systems

Strong knowledge and understanding of Current Good Manufacturing Practices (part of GxP)

Excellent oral and written communication skills

Working knowledge of MS Excel

Ability to manage complex issues and foster consensus among teams

Bonus Points If You Have (Preferred Requirements)

Experience in the pharmaceutical sector

Proficiency in technical writing and document reviews

Knowledge of contemporary technologies and best aseptic practices

Proactive approach to promoting safety within the workplace

Experience using common AI tools, including generative technologies such as 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.
Engineering
Job Classification
Industry: Pharmaceutical & Life Sciences
Functional Area / Department: Production, Manufacturing & Engineering
Role Category: Management
Role: Manufacturing Operations Manager
Employement Type: Full time
Contact Details:
Company: Pfizer
Location(s): Visakhapatnam

Apply

[Full Time] Associate Manager - Package Design & Development at Pfizer

Fri, 13 Mar 2026 04:00:11 +0530

Job Description
Use Your Power for Purpose

At Pfizer, we believe that every role contributes to our mission of improving patients lives. Whether you are involved in the design and development of manufacturing processes for products or supporting the upkeep of systems, engineering is crucial to ensuring customers and patients receive the medicines they need. By collaborating with our forward-thinking engineering team, youll play a pivotal role in accelerating the delivery of medicines to the world.

What You Will Achieve

Role Summary:

The role of Associate Manager Package design and development is to provide technical support on packaging development processes to production-packing and cross functional teams and troubleshoot exercise on packaging commodities and process. The packaging engineer is expected to develop packaging configurations and to manage technical efforts. Must be capable of ensuring resolution of all technical issues and providing timely implementation of all projects to maintain a consistent supply of our products to the market, while maintaining compliance with cGMP.

In this role, you will:

Develop plans for short-term work activities, including timelines, work plans, and deliverables within the team.

Provide technical support and guidance to ensure packaging systems comply with governmental regulations and meet customer and quality needs.

Collaborate with outside vendors and internal teams to develop and engineer packages that ensure functionality, compliance, cost-efficiency, and timely objectives.

Author and approve packaging specifications, pallet patterns, and bills of materials for various packaging systems.

Lead and support technical improvement projects aimed at defect reduction, improved equipment reliability, and better equipment utilization using Six Sigma and other tools.

Identify and implement cost-saving ideas, specifically efficiency improvements and projects that increase equipment capacity.

Communicate and participate in packaging material investigations, deviations, troubleshooting, corrective actions, and vendor capability assessments.

Provide technical support to the production-packing team for smooth product launches and support the Packaging Development Laboratory by procuring and maintaining testing equipment.

Here Is What You Need (Minimum Requirements)

Packaging related institute & degree with 5+ years of experience if diploma 7+ years of experience

Proficiency in Design Controls for Medical Devices and/or Combination Products

Strong skills in MS Office Suite

Solid understanding of Good Manufacturing Practices (GMP)

Experience with package labeling requirements, particularly in serialization, trade dress alignment, and batch variable imprinting methods, and their operational impacts

Ability to manage multiple projects simultaneously

Strong analytical and problem-solving skills

Bonus Points If You Have (Preferred Requirements)

Relevant sterile pharmaceutical packaging experience

Proficiency in continuous improvement and Statistical Process Control methodologies, such as DMAIC and Six Sigma

Familiarity with a wide range of package performance testing equipment and methods

Understanding of regional pharmaceutical compendia testing requirements

Excellent communication and interpersonal skills

Strong organizational skills and attention to detail

Demonstrated leadership capabilities and mentoring skills

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Engineering
Job Classification
Industry: Pharmaceutical & Life Sciences
Functional Area / Department: Production, Manufacturing & Engineering
Role Category: Management
Role: Manufacturing Operations Manager
Employement Type: Full time
Contact Details:
Company: Pfizer
Location(s): Visakhapatnam

Apply

[Full Time] Manufacturing Consultant (Cement) at Capgemini

Mon, 09 Mar 2026 12:00:00 +0530

Job Description
Your role
Act as a digital transformation leader and SME in Industrial manufacturing and cement industry Engineering and Plant Operations domain with good knowledge of day-to-day activities in industry
Act as a leader and build the team of consultants ready to be deployed on assignments. Ability to understand customer requirements and propose/develop/manage digital offers, develop go-to market strategy and identify key technology solutions and partnerships, present to global OEMs/ Industry players/customers with suitable business cases, considering the business objectives and ROI
Work with the sales team, customers and other stakeholders to generate business for Capgemini invent.Lead the engagements in the areas of digital continuity, engineering transformation, model-based systems engineering etc.
Articulate PoVs on relevant topics of the industry study and propose the future Industry trends to promote Thought leadership and Branding.Build and manage cross-functional teams to foster practice development and device market strategies to meet customer requirements around servitisation models or after-sales support that may involve new product/solution development
Your Profile
Possess strong interpersonal skills and problem-solving mindset to develop the customer relationship in business engagements and propose solutions based on your sound process/technology skills
Exposure to innovative IT/Product design & development techniques such as MBSE (Model based systems engineering), Agile/SAFe, with ability to leverage industry 4.0 technologies (such as IOT, cloud, AR/VR, Automation, Digital Twin, block chain, RFID) for creating customised offerings
8+ years of work experience in consulting plus Industrial - with emphasis on Engineering and Plant Operations consulting
Project Management experience and Business Consulting experience.
Job Classification
Industry: IT Services & Consulting
Functional Area / Department: Production, Manufacturing & Engineering
Role Category: Management
Role: Production / Manufacturing Head
Employement Type: Full time
Contact Details:
Company: Capgemini
Location(s): Mumbai

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[Full Time] Associate Manager- Manufacturing Compliance at Pfizer

Fri, 06 Mar 2026 12:00:00 +0530

Job Description
Why patients need you:

Our core principle and commitment towards the patients Patients lives depend 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 handling the responses to observations (Internal & External) and driving the inspection readiness program.

You will get a chance to be part of the projects or handle the small projects independently.

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:

Preparation of response to audit observations, propose CAPAs and take agreement between SME & Quality Assurance for identified items.

Preparation of Quality Risk Assessment (QRM) for the equipment & process and tracking the implementation of mitigation plan.

Responsible for the CCF initiation, coordination with CFTs for impact assessment and CCF pre-approval, implementation and closure.

Responsible to perform the gap assessment PQS/ CAS/ RONA & Others and propose the mitigation/ implementation of actions against the observed gaps.

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.

Driving a culture of continuous Inspection readiness

Ensuring all departments in manufacturing maintain compliant, audit-ready documentation

Conducting readiness assessments, mock audits, and gap analyses

Coordinating inspection logistics and cross-functional preparation

Supporting teams in understanding regulatory expectations

Tracking and following up on CAPAs, commitments, improvement actions from inspections readiness

Qualifications:

Must Have

Masters degree in Science

More than 7+ 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 QTS/ EQMS/ PDOCS/ SDS & SAP system.

Experience in Pharmaceuticals manufacturing

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.
Quality Assurance and Control
Job Classification
Industry: Pharmaceutical & Life Sciences
Functional Area / Department: Production, Manufacturing & Engineering
Role Category: Management
Role: Production / Manufacturing Head
Employement Type: Full time
Contact Details:
Company: Pfizer
Location(s): Visakhapatnam

Apply

[Full Time] Associate Manager at Pfizer

Sat, 21 Feb 2026 12:00:00 +0530

Job Description
Role and Responsibilities

Primary role is to drive Technology transfer activities including facility-fit assessment (process mapping), process optimization and operational readiness assessment and provide technical support as SME for successful scaleup of CRD projects in API development with internal & External CMO s.

Responsible person for an intermediate/API manufacturing development step in scale up.

Developing equipment fits for a multi-purpose API facility for new and existing products in existing equipment trains. e. g. successful tech. transfer from sister site of a new, high value, high demand API product for commercial scale-up and manufacture.

Providing end-to-end planning with respect to API supply commitments, short term for casting, including raw material delivery and API release.

Supporting HAZOP programs, FMEA and Continuous Improvement projects.

Design and develop safe manufacturing processes for APIs and their intermediates.

Critically assess the safety of processes intended for manufacture of APIs, and their intermediates, on laboratory, pilot plant and commercial manufacturing scales. This activity is critical to laboratory, pilot plant and commercial manufacturing activities.

Develop knowledge and experience of chemical reaction hazards, engineering principles and physical organic chemistry to be able to independently liaise with chemists to aid in the design of inherently safe processes and aid in solving process safety and scale-up related challenges as encountered.

Use process modeling software like Dynochem, Aspen plus, Visimix, DoE/Minitab software for development of scale up from lab to plant scale.

Familiarize in using PAT tools such as Crystal 16, FBRM, EasyViewer & BlazeMetrics for Crystallization studies and React IR on the Reaction kinetics.

Using statistical tools to identify, analyze, and interpret patterns and trends in complex data sets could be helpful for the diagnosis and prediction.

Provide technical/ Process engineering support for R&D and Plant such as corrosion study, mixing study, crystallization study, filtration study, Reaction kinetics and Kla studies for effective scale up.

Support CRD chemists for their Process engineering studies for scale up batches (Mixing from lab scale to plant scale, filtration studies using pocket filter for selection of filter and their Equipment mapping at higher scale. Handling hydrogenation and Kilo facilities for scale up batches.

Provide technical engineering support for process fit to plant workshops to ensure successful technology transfers of new products.

Sharing knowledge between sites with same/similar technology within Global network and Participation in global process technology networks.

SME in Process Engineering principles and operations with a flair for people management and development skills.

Collaboration with cross functional team for smooth and safe execution of projects across the sites.

Support technology transfer activities including process Optimization of infrastructure and operational readiness assessment.

Generation of process engineering report associated with Technology Transfer.

PREFERRED SKILLS

Excellent knowledge of chemical engineering unit operations and principles including reaction kinetics, reactor design, chemical thermodynamics, heat and mass transport, engineering statistics, modelling and simulation ( Dynochem, Aspen, Visimix etc) .

Excellent knowledge of downstream processing unit operations (extraction, distillation, crystallization, filtration/washing and drying)

Knowledge of equipment such as Reactors, filters, driers, centrifuges, mills, sieves and filter/driers.

Data collection and MINITAB analysis experience. Ability to develop data driven root cause analyses and solutions with strong problem-solving skills and an aptitude for learning systems quickly. Able to utilize structured problem-solving techniques such as DMAIC, Ishikawa (Fishbone diagram), Five Why (5W) or Lean six sigma . Able to resolve high level performance issues into addressable actions.

Strong ability to work and communicate effectively with team and peers within a manufacturing and Process R & D organization. This includes excellent communication skills: written and verbal.

Competent conducting chemical reactions, work ups and isolations in the laboratory to generate data

Track record of successfully developing manufacturing processes.

Excellent knowledge of scale dependent and independent parameters and how to manage scale-up and scale-down experiments.

Understanding and knowledge of process safety considerations when scaling processes.

Working knowledge of off-line and on-line analytical techniques (e. g. HPLC, MS, NMR, FTIR, FBRM, UV)

Minimum Qualification

Bachelor / master s degree in chemical engineering

Target years of experience

3 to 8 years of experience

Type of experience

Experience in a technical/functional role, Core Team member can be considered

Work Location Assignment: On Premise

Engineering

Job Classification
Industry: Pharmaceutical & Life Sciences
Functional Area / Department: Production, Manufacturing & Engineering
Role Category: Management
Role: Manufacturing Operations Manager
Employement Type: Full time
Contact Details:
Company: Pfizer
Location(s): Chennai

Apply

[Full Time] Group Manager - Packing at Pfizer

Wed, 04 Feb 2026 12:00:00 +0530

Job Description
Job Description:

Responsible for Packing operations schedule adherence as per assigned plan.

Review the production schedule in consultation with planning and functional head.

Deployment of manpower optimally and conduct/ensure on job training for newly joined employees.

Ensure the availability of packing materials for uninterrupted operations of equipment and optimization of energy utilization.

Attend the product quality review meetings and ensure effective intra-and-inter departmental communication.

Experience in facing regulatory inspections (USFDA, EU, TGA and ANVISA etc.)

Participate in the cross functional department meetings as and when required.

Preparation of department budget proposals.

Monitoring product standards and implementing quality and compliance programs.

Engage and inspire the team on performance expectations and coach the team to meet those expectations.

Focus on Safety and GMP Compliance as operational priorities and as performance measures that should be included in metrics.

Know the processes and procedures, including the principles and practices of good data management (ALCOA), and be able to guide, advise and coach the team.

Responsible for the Good Data Management and Data integrity understanding and performance of the team.

Daily presence in the Packing area to monitor the work activity and practices.

Lead and support continuous improvement practices/projects.

Review the content of all Leader Led Conversations with the teams aimed at fostering a culture that supports compliance with procedures, including good data management.

Plan manpower hiring requirements and participate in recruitment and onboarding.

Proven strong interpersonal skills.

Analytical thinking to grasp complex technical issues and ability to present to the auditors and leaders.

Decision making on activities in the area according to GMP procedures and Pfizer global policies.

Education Qualification:

Graduate or Postgraduate in Pharmacy or Science discipline.

Work Experience: 15+ years of experience in manufacturing parenteral dosage forms (Preferably in Packing domain)

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.
Manufacturing
Job Classification
Industry: Pharmaceutical & Life Sciences
Functional Area / Department: Production, Manufacturing & Engineering
Role Category: Management
Role: Manufacturing Operations Manager
Employement Type: Full time
Contact Details:
Company: Pfizer
Location(s): Visakhapatnam

Apply

[Full Time] Associate Manager - MES at Pfizer

Thu, 22 Jan 2026 01:51:56 +0530

Job Description
Qualifications
Must-Have

Graduate or Postgraduate in Pharmaceutical Science Discipline/Engineering.

Minimum 8+ years of experience.

Experience in manufacturing of pharmaceutical dosage forms (Sterile facility)

Strong background and knowledge in manufacturing operations, compliance processes and systems.

Experience and hand on electronic batch record design along with any associated software (i.e. FTPS (AMPS), SAP, MLM etc.) working exposure.

Technical knowledge of manufacturing and packaging operations and operation process flow.

Experience in defending process in regulatory audits /inspection.

Preferably experiences in good understanding of manufacturing and quality systems.

Effective communication skills are required, both written and verbal.

Must be comfortable working both independently and collaboratively.

Ability to communicate effectively with all cross functional teams (CFTs) within the organization.

Nice-to-Have
Masters degree
Previous experience on SAP and Electronic batch record designing. (FTPS, PAS|X)

Work Location Assignment: On Premise

Work Location Assignment: On Premise

Information & Business Tech

Job Classification
Industry: Pharmaceutical & Life Sciences
Functional Area / Department: Production, Manufacturing & Engineering
Role Category: Management
Role: Manufacturing Operations Manager
Employement Type: Full time
Contact Details:
Company: Pfizer
Location(s): Visakhapatnam

Apply

[Full Time] Associate Manager-Equipment Maintenance at Pfizer

Tue, 20 Jan 2026 12:00:00 +0530

Job Description
Use Your Power for Purpose

The Maintenance Engineer plays a critical role in ensuring the reliability, compliance, and optimal performance of process equipment used in pharmaceutical manufacturing. This position involves leading maintenance strategies, troubleshooting complex equipment issues, and ensuring adherence to GMP (Good Manufacturing Practices) and regulatory standards. The role requires close collaboration with production, quality assurance, and engineering teams to support uninterrupted manufacturing operations and continuous improvement initiatives

What You Will Achieve

In this role, you will:

Perform routine and preventive maintenance on Downstream areas: Sterilization, Visual Inspection, Packaging and Microbiology equipment.

Troubleshooting of Major technical issues & handle Complex technical issues of: Sterilization, Visual Inspection, Packaging and Microbiology equipment.

Lead and oversee preventive, predictive, and corrective maintenance activities for critical process equipment such as reactors, centrifuges, granulators, dryers, and tablet presses.

Ensure all maintenance activities comply with GMP, FDA, and other regulatory requirements.

Troubleshoot and resolve complex mechanical, electrical, and automation-related equipment issues.

Develop and optimize maintenance SOPs, checklists, and documentation in alignment with quality standards.

Coordinate with cross-functional teams during equipment qualification, validation, and change control processes.

Analyze equipment performance data to identify trends, root causes of failures, and opportunities for reliability improvement.

Manage spare parts inventory and vendor relationships for timely procurement and support.

Mentor junior engineers and technicians, and lead training initiatives on equipment maintenance best practices.

To perform FMEA & RCA and effectively trend equipment breakdowns and guide to implement corrective actions for improving reliability, heres a structured approach based on best practices in reliability engineering and maintenance management

Calibrate instruments such as pressure gauges, temperature sensors, flow meters, and analytical instruments.

Work with different types of PLCs, SCADA, and other PC based Automation systems used in pharmaceutical manufacturing.

Support for automation projects and equipment upgrades

Performing proactive maintenance activities to improve efficiency of downstream equipment.

Here Is What You Need (Minimum Requirements)

Qualification: D iploma or B. Tech in Instrumentation or Electronics Engineering.

Experience: Diploma with 10-12 years industrial experience or B. Tech with 7-8 years industrial experience.

Pharmaceutical Process Equipment Expertise
In-depth knowledge of operation, maintenance, and troubleshooting of equipment.

GMP & Regulatory Compliance
Strong understanding of Good Manufacturing Practices (GMP), FDA, MHRA, and other regulatory requirements governing pharmaceutical manufacturing.

Preventive & Predictive Maintenance
Proficient in developing and executing preventive and predictive maintenance strategies to minimize downtime and extend equipment life.

Root Cause Analysis (RCA)
Skilled in conducting failure investigations and implementing corrective and preventive actions (CAPA) to address recurring equipment issues.

Computerized Maintenance Management Systems (CMMS)
Hands-on experience with CMMS platforms for scheduling, tracking, and documenting maintenance activities.

Equipment Qualification & Validation Support
Familiar with IQ/OQ/PQ protocols and supporting validation activities for new and existing equipment.

Technical Documentation & SOP Development
Ability to create and maintain detailed maintenance SOPs, equipment logs, and compliance documentation.

Cross-Functional Collaboration
Effective communication and coordination with production, quality assurance, engineering, and external vendors.

Continuous Improvement & Reliability Engineering
Focused on identifying opportunities for process and equipment optimization using tools like FMEA, TPM, and Six Sigma

Bonus Points If You Have (Preferred Requirements)

Asset Lifecycle Management
Expertise in managing the full lifecycle of pharmaceutical equipment from procurement and installation to decommissioning ensuring cost-effectiveness and regulatory compliance.

Regulatory Audit Readiness
Proven ability to prepare for and support internal and external audits (e. g. , FDA, MHRA, WHO), including documentation, walkthroughs, and corrective action implementation.

Automation & Control Systems
Advanced knowledge of PLCs, SCADA, and DCS systems used in pharmaceutical manufacturing, with the ability to troubleshoot and optimize automated processes.

Risk-Based Maintenance Planning
Application of risk assessment tools (e. g. , FMEA, RCM) to prioritize maintenance activities based on criticality and impact on product quality and compliance.

Data-Driven Decision Making
Use of maintenance KPIs, OEE (Overall Equipment Effectiveness), and reliability metrics to drive continuous improvement and strategic planning.

Change Management & Engineering Projects
Leading equipment upgrades, retrofits, and technology transfers

Certification in Maintenance or Reliability Engineering

e. g. , Certified Maintenance & Reliability Professional (CMRP), Certified Reliability Engineer (CRE), or equivalent.

Knowledge of Validation Lifecycle

Understanding of validation lifecycle documentation (URS, DQ, IQ, OQ, PQ) and its integration with maintenance activities.

Project Management Skills

Experience in managing maintenance-related capital projects, including budgeting, scheduling, and resource allocation.

Exposure to Lean Manufacturing & Six Sigma

Application of lean tools and Six Sigma methodologies to reduce waste, improve equipment uptime, and enhance process efficiency.

SAP PM or Similar ERP Experience

Hands-on experience with enterprise systems for maintenance planning, work order management, and asset tracking.

Strong Documentation & Audit Trail Practices

Ability to maintain accurate and audit-ready records in line with ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, and more).

Training & Development Capabilities

Experience in developing training modules and conducting technical training for maintenance teams.

Work Location Assignment: On Premise

Engineering

Job Classification
Industry: Pharmaceutical & Life Sciences
Functional Area / Department: Production, Manufacturing & Engineering
Role Category: Management
Role: Maintenance Head
Employement Type: Full time
Contact Details:
Company: Pfizer
Location(s): Visakhapatnam

Apply