2,761 Manufacturing jobs in India

It’s not just about your career or job title… It’s about who you are and the impact you will make on the world. Because whether it’s for each other or our customers, we put People First. When our people come together, we Expand the Possible and continuously look for ways to improve what we create and how we do it. If you are constantly striving to grow, you’re in good company. We are revolutionizing the way the world moves for future generations, and we want someone who is ready to move with us.

Manufacturing Assembly / Soldering Technician:

Significant soldering experience is essential. IPC Certified Soldering Technician

with class 3 soldering expert.

Preferred PCBA rework specialist at least 2 years in relevant experience. Good eye-hand coordination to construct small parts and pieces into a final product Use of a soldering tool to solder parts. Requires precision to solder small items. The ability to use various hand tools to produce a final product Ability to follow instructions and Electrical diagrams as delivered for each product In-process Inspection and touch up of thru-hole and surface mount components using microscope. Knowledge of continuous improvement concepts like Kaizens, 5S etc. Familiarity with the use of Microsoft Excel, Word, Access, PowerPoint, and Outlook Effective oral and written communication skills Knowledge of problem-solving techniques like 7 QC tools, 5 Why Analysis etc. Maintain a safe working environment ensuring all company and regulatory
standards are always achieved.

Who are we?

Wabtec Corporation is a leading global provider of equipment, systems, digital solutions, and value-added services for freight and transit rail as well as the mining, marine, and industrial markets. Drawing on nearly four centuries of collective experience across Wabtec, GE Transportation, and Faiveley Transport, the company has grown to become One Wabtec, with unmatched digital expertise, technological innovation, and world-class manufacturing and services, enabling the digital-rail-and-transit ecosystems.

Wabtec is focused on performance that drives progress and unlocks our customers’ potential by delivering innovative and lasting transportation solutions that move and improve the world. We are lifelong learners obsessed with making things better to drive exceptional results. Wabtec has approximately 27K employees in facilities throughout the world. Visit our website to learn more!

Our Commitment to Embrace Diversity:

Wabtec is a global company that invests not just in our products, but also our people by embracing diversity and inclusion. We care about our relationships with our employees and take pride in celebrating the variety of experiences, expertise, and backgrounds that bring us together. At Wabtec, we aspire to create a place where we all belong and where diversity is welcomed and appreciated.

To fulfill that commitment, we rely on a culture of leadership, diversity, and inclusion. We aim to employ the world’s brightest minds to help us create a limitless source of ideas and opportunities. We have created a space where everyone is given the opportunity to contribute based on their individual experiences and perspectives and recognize that these differences and diverse perspectives make us better.

We believe in hiring talented people of varied backgrounds, experiences, and styles… People like you! Wabtec Corporation is committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or expression, or protected Veteran status. If you have a disability or special need that requires accommodation, please let us know.

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.

Location: Gandhinagar, Gujarat (On-site)

Job Title: Quality Control (QC) Engineer - Pharmaceutical Filtration Unit

Position Details

• Department: Quality Control

• Reporting To: Senior QC Engineer

• Experience Required: 3–5 years

• Employment Type: Full-time

• Working Days: 6 days/week

• Compensation: ₹6 – ₹6.5 LPA

Industry Preference (Mandatory)

Applicants must have prior work experience in at least one of the following regulated manufacturing sectors:

• Sterile/Injectables Manufacturing

• Medical Devices Manufacturing

• Medicinal Equipment Manufacturing

Contact -

Position Overview

We are looking for a proactive and detail-driven Quality Control (QC) Engineer with 3–5 years of experience in Sterile/Injectables, Medical Devices, or Medicinal Equipment manufacturing environments. This role is critical to ensuring consistent product quality through comprehensive analytical testing and adherence to stringent regulatory standards.

The ideal candidate will have hands-on expertise in chemical analysis, pharmacopeial testing, and GMP-compliant documentation, especially within a sterile or cleanroom environment.

Key Responsibilities

• Conduct routine testing of raw materials, in-process samples, and finished products in accordance with pharmacopeial guidelines (IP/BP/USP/Ph. Eur.).

• Perform detailed Pharma Copea Testing including identification, assay, dissolution, impurity profiling, and other analytical parameters.

• Execute general wet chemistry procedures along with pH and conductivity testing.

• Operate and calibrate analytical instruments including IR Spectroscopy, STIR, and related chemical analysis equipment.

• Ensure strict compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and internal Standard Operating Procedures (SOPs).

• Maintain complete and accurate documentation including test reports, calibration records, instrument logs, and change control records.

• Support investigations related to Out of Specification (OOS) and Out of Trend (OOT) results, including root cause analysis and CAPA.

• Liaise with Quality Assurance (QA), Production, and R&D teams for resolution of analytical issues and technical support.

• Prepare for and participate in internal and external audits, ensuring full laboratory compliance and readiness.

• Manage sample collection, labeling, storage, and contribute to stability studies where applicable.

Candidate Requirements

Educational Qualification (Preferred):

• B.Sc / M.Sc in Chemistry

• B.Pharm / M.Pharm with a focus on Pharmaceutical Chemistry

Experience:

• 3–5 years of relevant experience in a pharmaceutical or regulated manufacturing environment

• Must have worked in Sterile, Injectables, Medical Devices, or Medical Equipment manufacturing

Technical Skills:

• In-depth knowledge of pharmacopeial testing methods and documentation practices

• Hands-on experience with IR Spectroscopy, STIR, pH meters, and conductivity meters

• Familiarity with analytical method validation and instrument calibration

• Strong understanding of Data Integrity, GDP (Good Documentation Practices), and compliance in regulated cleanroom settings

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.

Location: Gandhinagar, Gujarat (On-site)

Job Title: Quality Control (QC) Engineer - Pharmaceutical Filtration Unit

Position Details

• Department: Quality Control

• Reporting To: Senior QC Engineer

• Experience Required: 3–5 years

• Employment Type: Full-time

• Working Days: 6 days/week

• Compensation: ₹6 – ₹6.5 LPA

Industry Preference (Mandatory)

Applicants must have prior work experience in at least one of the following regulated manufacturing sectors:

• Sterile/Injectables Manufacturing

• Medical Devices Manufacturing

• Medicinal Equipment Manufacturing

Contact -

Position Overview

We are looking for a proactive and detail-driven Quality Control (QC) Engineer with 3–5 years of experience in Sterile/Injectables, Medical Devices, or Medicinal Equipment manufacturing environments. This role is critical to ensuring consistent product quality through comprehensive analytical testing and adherence to stringent regulatory standards.

The ideal candidate will have hands-on expertise in chemical analysis, pharmacopeial testing, and GMP-compliant documentation, especially within a sterile or cleanroom environment.

Key Responsibilities

• Conduct routine testing of raw materials, in-process samples, and finished products in accordance with pharmacopeial guidelines (IP/BP/USP/Ph. Eur.).

• Perform detailed Pharma Copea Testing including identification, assay, dissolution, impurity profiling, and other analytical parameters.

• Execute general wet chemistry procedures along with pH and conductivity testing.

• Operate and calibrate analytical instruments including IR Spectroscopy, STIR, and related chemical analysis equipment.

• Ensure strict compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and internal Standard Operating Procedures (SOPs).

• Maintain complete and accurate documentation including test reports, calibration records, instrument logs, and change control records.

• Support investigations related to Out of Specification (OOS) and Out of Trend (OOT) results, including root cause analysis and CAPA.

• Liaise with Quality Assurance (QA), Production, and R&D teams for resolution of analytical issues and technical support.

• Prepare for and participate in internal and external audits, ensuring full laboratory compliance and readiness.

• Manage sample collection, labeling, storage, and contribute to stability studies where applicable.

Candidate Requirements

Educational Qualification (Preferred):

• B.Sc / M.Sc in Chemistry

• B.Pharm / M.Pharm with a focus on Pharmaceutical Chemistry

Experience:

• 3–5 years of relevant experience in a pharmaceutical or regulated manufacturing environment

• Must have worked in Sterile, Injectables, Medical Devices, or Medical Equipment manufacturing

Technical Skills:

• In-depth knowledge of pharmacopeial testing methods and documentation practices

• Hands-on experience with IR Spectroscopy, STIR, pH meters, and conductivity meters

• Familiarity with analytical method validation and instrument calibration

• Strong understanding of Data Integrity, GDP (Good Documentation Practices), and compliance in regulated cleanroom settings

Title: VP-Manufacturing

Location: Ahemdabad

Role Objective

The objective of this job role is to provide strategic leadership and vision to the manufacturing operations of the Organisation. Develop and implement operational strategies to improve efficiency, productivity, and profitability. Create Annual Operating Plan (AOP) to support the strategic direction. Develop SOP to ensure maximum capacity utilization for overall productivity. Plan and forecast resources for facilities, equipment, materials, technology, and workforce to ensure sufficient manufacturing capacity to ensure support business goals. Translate strategy into actionable steps for growth, implementing goal setting and performance management across plants. Employ strategies to maximize customer satisfaction and manage marketing initiatives.

Lead all Plant operations and expansion projects in the future. Work closely with the Plant heads in order to optimise efficiencies and continuously improve on product delivery. Develop and incorporates solid operational safety, regulatory compliance, quality assurance, and cost control policies and programs into all manufacturing processes. Analyse financial and operational data to identify areas for improvement.

GENERAL RESPONSIBILITIES:

MANUFACTURING

ENGINEERING & MAINTENANCE

Accountable to maintain overall plants including all equipment, machineries at highest level with the proper preventive maintenance plan execution through maintenance in-charge.

TEAM LEADERSHIP:

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