11 Manufacturing jobs in Kota

• Standardize process improvement approach across units to achieve consistent and sustainable results across the business.
• Demonstrate rigor in implementation of Global ManEx processes and standards, via annual alignment review.
• Guide auditable improvement in employee technical capabilities, understanding of required processes and culture shift with sustained results, via annual unit audits.
• Develop specific manufacturing performance improvement initiatives to optimize cost, eliminate waste and improve operational flexibility.

• Standardize process improvement approach across units to achieve consistent and sustainable results across the business.
• Demonstrate rigor in implementation of Global ManEx processes and standards, via annual alignment review.
• Guide auditable improvement in employee technical capabilities, understanding of required processes and culture shift with sustained results, via annual unit audits.
• Develop specific manufacturing performance improvement initiatives to optimize cost, eliminate waste and improve operational flexibility.

Hi,

We are having an opening for Senior Manager, Business Analyst-SAP Manufacturing for our IT team at our Mumbai location

Job Summary :

The SAP Manufacturing BA will be responsible for ensuring that IT initiatives within the domain of Manufacturing align with the organizations global business objectives. This role involves collaboration between IT and business units and to drive innovation across various regions and functions within Manufacturing and allied areas like QM, WM etc. The role holder will ensure effective bridging between IT and Business, ensuring that all the business requirements are properly captured, documented and translated for effective solution execution. The role would involve appropriate PMO activities for ensuring smooth delivery of tech solution for desired business impact

Areas Of Responsibility :

• Strategic Business Alignment: In this role, you will lead comprehensive efforts to align IT strategies with business objectives, wrt manufacturing domain. You will work closely with senior leadership to identify and prioritize IT initiatives that support business goals, ensuring that IT investments are aligned with the organization's strategic priorities. You will form the bridge between IT and business and be responsible for translating the business requirements into executable IT solutions. Simultaneously ensuring PMO and delivery excellence for entire SAP Manufacturing, QM and WM domain will be built into your KRA.
• Business Partnership: You will collaborate with business stakeholders to identify and document the requirements. After that you need to liaison with the IT and Platform SMEs to brainstorms and arrive at the solution approach. Post that execution needs to be scheduled and delivered. You need to play an active role in testing. The primary KRA for this position is to ensure that the business requirements are delivered on time and as per expectations.
• Project Governance and Budget Ownership: You will work to define and scope IT initiatives in manufacturing domain and ensure quality delivery on time and within approved costs and efforts. Overseeing the development of strategic IT roadmaps and managing budgets for large-scale projects will be a critical part of your responsibilities. You will work closely with project managers and ITBPs to develop detailed project plans, monitor progress, and ensure that projects are delivered on time and within budget.

Educational Qualification : Bachelor in IT or Master of Business Administration (preferred)

Skills : Business Analysis, Project Management, Business partnership, relationship management, strategic alignment

Experience : 6-8+ years in IT Business Analysis or ITBP

Job Title: Manufacturing Engineer – Medical Devices (Senior/Principal Level)(Remote)

Location: Hyderabad, IND

Employment Type: Part-time

Position Summary:

We are seeking an experienced Manufacturing Engineer Trainer with 10+ years of hands-on expertise in the medical device industry to support and enhance our manufacturing operations. The ideal candidate will have a proven track record in process development, validation, scale-up, and continuous improvement while ensuring compliance with FDA, ISO 13485, and GMP regulations .

Key Responsibilities:

• Lead the design, development, and optimization of manufacturing processes for Class II/III medical devices.
• Drive process validation activities, including IQ, OQ, PQ, and Test Method Validation in compliance with regulatory requirements.
• Collaborate with R&D, Quality, and Regulatory teams to ensure smooth transfer of products from design to full-scale manufacturing.
• Identify, analyze, and resolve complex manufacturing challenges to improve efficiency, cost-effectiveness, and product quality.
• Oversee equipment selection, installation, and qualification (IQ/OQ/PQ), ensuring robust process capability.
• Lead continuous improvement initiatives using Lean, Six Sigma, and other structured problem-solving methodologies.
• Provide technical leadership and mentorship to junior engineers and technicians.
• Support audits (internal, supplier, and regulatory) by preparing technical documentation and ensuring compliance with ISO 13485, FDA 21 CFR Part 11/820, and EU MDR .
• Manage nonconformance investigations, root cause analysis, and corrective/preventive actions (CAPA) .
• Collaborate with suppliers to ensure incoming materials meet specifications and quality standards.

Qualifications:

• Bachelor’s degree in Mechanical, Biomedical, Manufacturing, or related Engineering field (Master’s preferred).
• 10+ years of progressive experience in manufacturing engineering within the medical device industry.
• Strong background in process validation, design transfer, and GMP manufacturing operations .
• Proficiency in Lean Manufacturing, Six Sigma (Green/Black Belt preferred).
• Experience with CAD software, statistical analysis tools, and ERP/MES systems.
• In-depth knowledge of FDA, ISO 13485, ISO 14971, and EU MDR regulations .
• Demonstrated leadership in cross-functional teams and mentoring junior staff.
• Excellent communication, documentation, and project management skills.

Dear Candidates, Please note, we will be able to respond to only those candidates, whose cvs are shortlisted. We respect your valuable time for applying.

Job Role - Factory Manager

Expectation -Leadership Skills

Salary - 20LPA

Location - Bhakrahat, Kolkatta

Contact

Our client is seeking an experienced Factory Manager to lead and oversee daily operations at their Bakrahat manufacturing facility. Ideal candidates will

have a background in machinery manufacturing, metal-oriented product manufacturing, or similar industries, and must demonstrate a track record of

career longevity.

Key Responsibilities:

Oversee and manage daily operations of the factory to ensure efficiency, safety, and productivity.

Develop and implement production plans, schedules, and budgets to meet output targets on time and within budget.

Lead, train, and supervise production staff across all facility departments.

Conduct periodic inspections to monitor staff performance, machinery condition, and adherence to quality standards.

Collaborate with quality control teams to enforce quality assurance protocols and continuously improve product standards.

Maintain equipment and machinery to ensure optimal working condition and minimize downtime.

Implement and monitor safety policies, ensuring compliance with all statutory and industry regulations.

Coordinate with internal teams for raw material supply, logistics, and timely delivery of finished goods.

Prepare and present regular production performance reports to senior management.

Foster a positive, productive work environment and actively resolve operational issues.

Requirements:

Bachelor's degree in Engineering, Industrial Management, Business Administration, or related discipline; advanced degree preferred.

5+ years managerial experience in a factory setting; background in machinery, metal products, or similar manufacturing highly desired.

Demonstrable career stability and progression in past roles.

Strong leadership, communication, and team-building skills.

Knowledge of production management, maintenance protocols, quality standards, and safety systems.

Proficiency with ERP systems, production management software, and Microsoft Office.

Expertise in lean manufacturing, Six Sigma, or similar process optimization methodologies preferred.

Preferred Skills:

Problem-solving and analytical abilities, especially for process troubleshooting and production improvement.

Flexibility and adaptability in rapidly changing environments.

Proven negotiation skills for interacting with suppliers and vendors.

Commitment to continuous learning and industry best-practices.

Ideal Profile:

Prior experience in machinery manufacturing, metal fabrication, or related industries (aluminum, steel, equipment, etc.).

History of long-term employment and professional advancement in previous roles.

Ability to mentor and build high-performing teams in a factory environment.

Location: Bakrahat, West Bengal.

This role offers an excellent opportunity to lead a modern manufacturing facility with our client, focusing on operational excellence and high product

quality in a supportive environment.

About Collabrix Inc.

Collabrix Inc. is a rapidly growing SaaS company headquartered in Texas and serving life sciences enterprises worldwide. Our products enable seamless collaboration between pharmaceutical and biotechnology companies and their global manufacturing partners. As a virtual-first company with a team based in India, we combine domain depth and technical agility to solve complex problems that matter.

Role Overview

We are seeking an Integration Analyst with deep expertise in designing and implementing enterprise integrations across supply chain, manufacturing, and industrial automation environments. The ideal candidate will have strong working knowledge of industry standards such as ISA-95 and ISA-88, coupled with practical experience in Industry 4.0 architectures, ERP, MES, and automation systems.

This role requires a hands-on professional who can bridge business processes and technical integration patterns, ensuring data flows seamlessly between enterprise platforms and shop-floor systems. You will work closely with product managers, engineers, and client IT/OT teams to design robust, scalable, and compliant integrations that enable digital transformation in life sciences manufacturing.

Key Responsibilities

• Design, develop, and implement integration solutions between ERP, MES, supply chain platforms, and industrial automation systems.
• Apply standards such as ISA-95 and ISA-88 in integration design, ensuring consistency and interoperability.
• Architect and implement Industry 4.0–ready integration frameworks to support smart manufacturing and connected supply chains.
• Collaborate with client IT/OT teams to define requirements, map data flows, and establish secure communication protocols.
• Leverage APIs, middleware, ESBs, and modern integration tools for scalable deployments.
• Ensure compliance with regulatory frameworks (GxP, 21 CFR Part 11, data integrity).
• Troubleshoot and optimize integration performance, reliability, and scalability.
• Document integration architecture, specifications, and operating procedures.
• Support product roadmap by advising on integration best practices and emerging technologies.

Required Skills & Experience

• 5–10 years of experience in system integration, industrial automation, or manufacturing IT/OT.
• Expertise in ISA-95 (Enterprise-Control System Integration) and ISA-88 (Batch Control) standards.
• Hands-on experience with ERP (SAP, Oracle, etc.), MES, and supply chain solutions.
• Familiarity with industrial automation technologies (PLC, SCADA, DCS) and data exchange protocols (OPC UA, MQTT, etc.).
• Exposure to Industry 4.0 technologies such as IoT, digital twins, and advanced analytics.
• Strong knowledge of integration platforms (e.g., Apache Camel, MuleSoft, Dell Boomi, or similar).
• Solid understanding of regulatory compliance in life sciences manufacturing (GxP, GMP).
• Excellent problem-solving, documentation, and communication skills.
• Bachelor’s/Master’s degree in Engineering, Computer Science, or related field.

What We Look For

• A systems thinker who understands both IT and OT domains.
• Ability to translate complex manufacturing workflows into integration designs.
• Strong collaboration and communication skills for working with global client teams.
• Commitment to quality, compliance, and reliability in mission-critical integrations.
• Passion for enabling digital transformation in life sciences.

Work Schedule

To support our global customers with agility and excellence, we follow a six-day work model on alternate weeks. Employees are expected to work on the 1st, 3rd, and 5th Saturdays of each month. This helps us accelerate delivery timelines while maintaining high standards of quality.

Why Join Collabrix

• Be at the forefront of digital manufacturing and supply chain transformation.
• Work with global enterprise clients and cutting-edge technologies.
• High ownership, visibility, and flexibility in a growing SaaS startup.
• Collaborative and transparent remote-first culture.
• Long-term career growth opportunities as we scale.

To Apply

Send your résumé and a brief note on why you’d be a great fit to

We are looking for an expert in Albumin and Immunoglobulin production to join us as a Consultant , with the opportunity to transition into a full-time Director of Albumin & Immunoglobulin Production as we expand.

This is a unique chance to help shape and lead a cutting-edge biologics manufacturing program with long-term impact.

As a consultant, you will:

• Guide us in designing and scaling manufacturing processes for Albumin and Immunoglobulins.
• Advise on technology selection, facility setup, and equipment procurement .
• Ensure compliance with cGMP, FDA, EMA, DCGI, ICH, and WHO guidelines .
• Support regulatory filings (IND, BLA, DMF, etc.) and strengthen legal/regulatory compliance.
• Implement quality assurance and quality control systems .
• Mentor and train internal teams to build long-term organisational expertise.

On successful engagement, you will transition into the Director role , leading operations, strategy, and global compliance for our Albumin & Immunoglobulin division.

• Advanced degree (M.Sc./PhD in Biotechnology, Biochemistry, or related field).
• 10+ years’ experience in biologics manufacturing, with specific expertise in Albumin and Immunoglobulins.
• Proven track record in large-scale plasma fractionation or recombinant protein production .
• In-depth knowledge of regulatory frameworks (FDA, EMA, DCGI, ICH, WHO).
• Strong leadership qualities with the potential to scale into a Director role.

• Experience engaging with regulatory authorities .
• Familiarity with intellectual property, licensing, and compliance in biologics.
• Knowledge of market access and global trade regulations .

(on-site/hybrid/remote consulting acceptable initially)

• Phase 1: Consultant (part-time/flexible, project-based).
• Phase 2: Full-time Director of Albumin & Immunoglobulin Production.

If you have the expertise and vision to lead Albumin & Immunoglobulin manufacturing into the future, we’d love to hear from you.

Please send your CV and a short cover note highlighting relevant projects and achievements to:

We are looking for an expert in Albumin and Immunoglobulin production to join us as a Consultant , with the opportunity to transition into a full-time Director of Albumin & Immunoglobulin Production as we expand.

This is a unique chance to help shape and lead a cutting-edge biologics manufacturing program with long-term impact.

As a consultant, you will:

• Guide us in designing and scaling manufacturing processes for Albumin and Immunoglobulins.
• Advise on technology selection, facility setup, and equipment procurement .
• Ensure compliance with cGMP, FDA, EMA, DCGI, ICH, and WHO guidelines .
• Support regulatory filings (IND, BLA, DMF, etc.) and strengthen legal/regulatory compliance.
• Implement quality assurance and quality control systems .
• Mentor and train internal teams to build long-term organisational expertise.

On successful engagement, you will transition into the Director role , leading operations, strategy, and global compliance for our Albumin & Immunoglobulin division.

• Advanced degree (M.Sc./PhD in Biotechnology, Biochemistry, or related field).
• 10+ years’ experience in biologics manufacturing, with specific expertise in Albumin and Immunoglobulins.
• Proven track record in large-scale plasma fractionation or recombinant protein production .
• In-depth knowledge of regulatory frameworks (FDA, EMA, DCGI, ICH, WHO).
• Strong leadership qualities with the potential to scale into a Director role.

• Experience engaging with regulatory authorities .
• Familiarity with intellectual property, licensing, and compliance in biologics.
• Knowledge of market access and global trade regulations .

(on-site/hybrid/remote consulting acceptable initially)

• Phase 1: Consultant (part-time/flexible, project-based).
• Phase 2: Full-time Director of Albumin & Immunoglobulin Production.

If you have the expertise and vision to lead Albumin & Immunoglobulin manufacturing into the future, we’d love to hear from you.

Please send your CV and a short cover note highlighting relevant projects and achievements to:

Job title: Quality Control Manager
Location: Hyderabad, India (Onsite)

The client is a robotics company creating intelligent, self-climbing robots for urban use, designed to clean skyscraper windows without human help. Their in-house solution combines custom hardware, advanced AI, and proprietary software, now moving into large-scale production.

We're looking for an experienced Quality Control Manager to lead our quality assurance processes as we scale from development to large-scale production. You'll work closely with hardware, software, and AI teams to ensure our products meet the highest standards for safety, reliability, and performance.

Key Responsibilities:

• Develop and lead quality strategies for hardware and software.
• Oversee testing, validation, inspection, and compliance processes.
• Collaborate across R&D, manufacturing, and supplier teams.
• Lead, train, and mentor the quality control team.
• Drive ISO certifications and regulatory compliance.

Requirements:

• 10+ years in quality control/assurance, ideally in robotics, automation, or aerospace.
• Strong expertise in both hardware and software quality management.
• Experience with Six Sigma, Lean Manufacturing, and AI-powered systems is a plus.
• Excellent leadership, problem-solving, and communication skills.
• Bachelor's or Master's in Mechanical Engineering, Robotics, Electronics, or related fields.

Be part of something groundbreaking. Let's build the future of urban robotics together. Apply now!