25 Pharmaceutical Production jobs in India

Automation Engineer – Pharmaceutical Manufacturing

Bengaluru, Karnataka Tek Support

Posted 1 day ago

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Job Description

Job Title: Senior Automation Engineer Trainer – Pharmaceutical Manufacturing

Location: Remote

Experience: 10+ years

Industry: Pharmaceutical / Biotech Manufacturing


Job Summary:

The Senior Automation Engineer Trainer is responsible for driving automation initiatives across pharmaceutical manufacturing systems, ensuring compliance with GMP, and enhancing equipment reliability and process efficiency. This role involves overseeing automation design, programming, validation, and maintenance of PLC, SCADA, and related control systems used in production and utility areas.

Key Responsibilities:

  • Managed automation systems supporting production, utilities, and cleanroom environments in compliance with GMP and regulatory requirements.
  • Developed, modified, and optimized control logic for PLC, HMI, and SCADA systems (Siemens, Allen-Bradley, DeltaV, or equivalent).
  • Supported the design, configuration, and integration of new automated equipment and systems into existing production lines.
  • Performed troubleshooting and root cause analysis of automation and instrumentation failures to minimize downtime.
  • Executed system upgrades, patches, and changes following change control procedures and validation standards (GAMP 5).
  • Prepared and reviewed technical documentation including URS, FDS, FAT, SAT, IQ/OQ/PQ, and SOPs.
  • Ensured data integrity and compliance with 21 CFR Part 11 for electronic records and automation systems.
  • Collaborated with cross-functional teams (Engineering, QA, Validation, and Manufacturing) for project execution and continuous improvement.
  • Guided junior engineers and technicians in automation programming, troubleshooting, and documentation practices.
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Bioprocess Engineer - Pharmaceutical Manufacturing

530001 Visakhapatnam, Andhra Pradesh ₹900000 Annually WhatJobs

Posted 7 days ago

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Job Description

full-time
Our client, a rapidly expanding biopharmaceutical company, is seeking an accomplished Bioprocess Engineer to contribute to its innovative manufacturing operations in Visakhapatnam, Andhra Pradesh . This role is integral to the development, scale-up, and optimization of biopharmaceutical manufacturing processes. You will be responsible for designing, validating, and troubleshooting complex bioreactor systems and downstream processing operations. The ideal candidate will possess a strong foundation in biochemical engineering principles, fermentation technology, and sterile processing. You will work collaboratively with research and development teams, quality assurance, and manufacturing personnel to ensure product quality and process efficiency. Key responsibilities include process monitoring, data analysis, implementation of process improvements, and ensuring compliance with regulatory standards (cGMP). This is a hands-on role that requires meticulous attention to detail, strong analytical skills, and the ability to solve intricate engineering challenges. Opportunities for professional growth and exposure to cutting-edge bioprocessing technologies are abundant.

Key Responsibilities:
  • Design, develop, and scale up biopharmaceutical manufacturing processes.
  • Optimize bioreactor performance, including media formulation, inoculation strategies, and operating parameters.
  • Oversee downstream purification processes such as filtration, chromatography, and viral inactivation.
  • Validate new equipment and processes according to cGMP guidelines.
  • Troubleshoot process deviations and implement corrective and preventative actions (CAPAs).
  • Monitor process performance using data acquisition systems and statistical process control.
  • Author and review technical documents, including batch records, SOPs, and validation protocols.
  • Collaborate with cross-functional teams to ensure seamless technology transfer from R&D to manufacturing.
  • Ensure compliance with all relevant regulatory requirements and quality standards.
  • Identify and implement process improvements to enhance efficiency, yield, and product quality.

Qualifications:
  • Bachelor's or Master's degree in Biochemical Engineering, Chemical Engineering, or a related field.
  • Minimum of 3-5 years of experience in biopharmaceutical process development or manufacturing.
  • Hands-on experience with microbial fermentation and/or mammalian cell culture processes.
  • Proficiency in downstream processing techniques (e.g., chromatography, tangential flow filtration).
  • Understanding of cGMP regulations and validation principles.
  • Strong analytical and problem-solving skills.
  • Excellent written and oral communication skills.
  • Ability to work effectively in a team environment and independently.
  • Experience with process modeling and simulation software is a plus.
This advertiser has chosen not to accept applicants from your region.

Automation Engineer Trainer – Pharmaceutical Manufacturing

Delhi, Delhi Tek Support

Posted 1 day ago

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Job Description

Job Title: Senior Automation Engineer Trainer – Pharmaceutical Manufacturing

Location: Remote

Experience: 10+ years

Industry: Pharmaceutical / Biotech Manufacturing


Job Summary:

The Senior Automation Engineer Trainer is responsible for driving automation initiatives across pharmaceutical manufacturing systems, ensuring compliance with GMP, and enhancing equipment reliability and process efficiency. This role involves overseeing automation design, programming, validation, and maintenance of PLC, SCADA, and related control systems used in production and utility areas.


Key Responsibilities:

  • Managed automation systems supporting production, utilities, and cleanroom environments in compliance with GMP and regulatory requirements.
  • Developed, modified, and optimized control logic for PLC, HMI, and SCADA systems (Siemens, Allen-Bradley, DeltaV, or equivalent).
  • Supported the design, configuration, and integration of new automated equipment and systems into existing production lines.
  • Performed troubleshooting and root cause analysis of automation and instrumentation failures to minimize downtime.
  • Executed system upgrades, patches, and changes following change control procedures and validation standards (GAMP 5).
  • Prepared and reviewed technical documentation including URS, FDS, FAT, SAT, IQ/OQ/PQ, and SOPs.
  • Ensured data integrity and compliance with 21 CFR Part 11 for electronic records and automation systems.
  • Collaborated with cross-functional teams (Engineering, QA, Validation, and Manufacturing) for project execution and continuous improvement.
  • Guided junior engineers and technicians in automation programming, troubleshooting, and documentation practices.
This advertiser has chosen not to accept applicants from your region.

Senior Process Engineer - Pharmaceutical Manufacturing

248001 Dehradun, Uttarakhand ₹1050000 Annually WhatJobs

Posted 2 days ago

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Job Description

full-time
Our client is a leading pharmaceutical company recognized for its commitment to quality and innovation in drug manufacturing. We are seeking a highly experienced Senior Process Engineer to join our state-of-the-art facility in Dehradun, Uttarakhand, IN . This role is essential for optimizing and ensuring the efficiency, safety, and compliance of our manufacturing processes. The ideal candidate will have a strong background in chemical engineering principles, process design, validation, and scale-up within a GMP (Good Manufacturing Practice) environment.

As a Senior Process Engineer, you will be responsible for the continuous improvement of existing manufacturing processes, troubleshooting operational issues, and leading the design and implementation of new process technologies. You will conduct process hazard analyses, develop Standard Operating Procedures (SOPs), and ensure adherence to all regulatory requirements. Collaboration with R&D, Quality Assurance, Production, and Maintenance teams will be critical to achieving operational excellence. This position requires a proactive approach to identifying and implementing process enhancements that improve yield, reduce costs, and enhance product quality. You will also play a key role in validation activities, including IQ/OQ/PQ of new equipment and processes. The ability to lead cross-functional teams and manage projects effectively is crucial.

Responsibilities:
  • Design, develop, and optimize chemical and pharmaceutical manufacturing processes.
  • Troubleshoot and resolve process-related issues to ensure continuous operation and product quality.
  • Lead process improvement initiatives to enhance efficiency, yield, and cost-effectiveness.
  • Conduct process hazard analyses (PHAs) and implement safety improvements.
  • Develop and revise Standard Operating Procedures (SOPs) and batch records.
  • Oversee and participate in the validation of new equipment and processes (IQ/OQ/PQ).
  • Collaborate with R&D to scale up new products and processes from laboratory to commercial production.
  • Ensure all processes comply with GMP, FDA, and other relevant regulatory guidelines.
  • Work closely with Production, Quality Assurance, and Maintenance departments to address operational challenges.
  • Train production personnel on new processes and equipment.
  • Analyze process data to identify trends, root causes of deviations, and opportunities for optimization.
  • Prepare technical reports, process documentation, and presentations.
  • Stay current with industry best practices and emerging technologies in pharmaceutical manufacturing.
  • Manage process engineering projects, including scope, budget, and timelines.
Qualifications:
  • Bachelor's or Master's degree in Chemical Engineering or a related discipline.
  • Minimum of 6-8 years of experience in process engineering within the pharmaceutical or biotechnology industry.
  • In-depth knowledge of GMP regulations and validation principles.
  • Experience with various manufacturing unit operations (e.g., reaction, filtration, drying, granulation, tablet compression, sterile filling).
  • Proficiency in process simulation software and data analysis tools.
  • Strong analytical, problem-solving, and critical thinking skills.
  • Excellent written and verbal communication skills.
  • Proven ability to lead projects and cross-functional teams.
  • Experience with process safety management (PSM).
  • Familiarity with Lean Manufacturing or Six Sigma methodologies is a plus.
Join our team in Dehradun, Uttarakhand, IN and contribute to the advancement of life-saving pharmaceuticals.
This advertiser has chosen not to accept applicants from your region.

Senior Pharmaceutical Manufacturing Operations Lead

400601 Thane, Maharashtra ₹130000 Monthly WhatJobs

Posted 2 days ago

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Job Description

full-time
Our client, a renowned pharmaceutical innovator, is seeking a highly experienced Senior Pharmaceutical Manufacturing Operations Lead to spearhead their production excellence from a remote capacity. This critical role involves overseeing and optimizing all aspects of pharmaceutical manufacturing operations, ensuring adherence to the highest global standards of quality, safety, and efficiency. The ideal candidate will possess a profound understanding of cGMP, advanced manufacturing technologies, and lean operational principles. You will be responsible for strategic planning, process improvement, team leadership, and driving the successful execution of manufacturing campaigns. This is a unique opportunity to influence manufacturing strategy and operations across the organization, working remotely with cross-functional teams.

Responsibilities:
  • Lead and manage day-to-day pharmaceutical manufacturing operations, ensuring compliance with cGMP, regulatory requirements, and company policies.
  • Develop and implement strategic plans to enhance manufacturing efficiency, throughput, and cost-effectiveness.
  • Oversee the production lifecycle from raw material receiving through to final product packaging and release.
  • Implement and champion lean manufacturing principles and continuous improvement initiatives (e.g., Six Sigma).
  • Manage production schedules, resource allocation, and operational budgets effectively.
  • Ensure robust quality control and quality assurance processes are integrated into all manufacturing activities.
  • Lead, mentor, and develop a high-performing manufacturing team, fostering a culture of accountability and continuous learning.
  • Drive process validation and optimization projects to improve yield, reduce waste, and enhance product quality.
  • Collaborate closely with R&D, Engineering, Supply Chain, and Quality Assurance departments to ensure seamless operations.
  • Develop and maintain strong relationships with key equipment vendors and service providers.
  • Oversee and manage operational health and safety programs to ensure a safe working environment.
  • Prepare and present operational performance reports, key metrics, and strategic recommendations to senior leadership.
Qualifications:
  • Master's degree in Chemical Engineering, Pharmaceutical Sciences, Biotechnology, or a related technical field.
  • Minimum of 10 years of progressive experience in pharmaceutical manufacturing operations, with a significant track record in leadership roles.
  • In-depth knowledge of cGMP regulations, regulatory guidelines (e.g., FDA, EMA, ICH), and pharmaceutical manufacturing best practices.
  • Proven experience in leading large-scale manufacturing operations and managing complex production processes.
  • Strong understanding of process validation, sterile manufacturing, API production, or finished dosage forms.
  • Expertise in implementing lean manufacturing principles and driving operational excellence.
  • Exceptional leadership, communication, problem-solving, and decision-making skills.
  • Demonstrated ability to manage budgets and P&L responsibilities.
  • Experience with process automation, MES, and ERP systems.
  • Ability to thrive and lead effectively in a fully remote work environment.
This role offers a chance to make a substantial impact on global pharmaceutical production from a strategic remote position.
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Senior Process Engineer - Pharmaceutical Manufacturing

400001 Mumbai, Maharashtra ₹120000 Annually WhatJobs

Posted 3 days ago

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Job Description

full-time
Our client, a leading pharmaceutical manufacturing company, is seeking an experienced Senior Process Engineer to join their dynamic and innovative team. This is a fully remote position, offering the flexibility to work from anywhere while contributing to critical manufacturing processes in the pharmaceutical sector. You will play a key role in optimizing production efficiency, ensuring product quality, and driving process improvements within our state-of-the-art facilities. This role requires a deep understanding of chemical engineering principles and a strong track record in process optimization within a highly regulated environment.

Key Responsibilities:
  • Design, develop, and optimize manufacturing processes for pharmaceutical products, ensuring compliance with cGMP and other regulatory standards.
  • Analyze process data to identify inefficiencies, troubleshoot issues, and implement corrective actions.
  • Lead process validation activities, including protocol development, execution, and reporting.
  • Develop and maintain Standard Operating Procedures (SOPs) for all manufacturing processes.
  • Collaborate with R&D, Quality Assurance, and Production teams to ensure seamless technology transfer and scale-up.
  • Implement process improvements to enhance yield, reduce waste, and lower manufacturing costs.
  • Conduct risk assessments and implement mitigation strategies for process-related hazards.
  • Provide technical expertise and support to manufacturing operations.
  • Stay current with industry trends, new technologies, and best practices in pharmaceutical manufacturing.
  • Develop and deliver training programs to production personnel on process operations and safety.
  • Contribute to the design and qualification of new equipment and facility modifications.
Qualifications:
  • Bachelor's or Master's degree in Chemical Engineering, Pharmaceutical Engineering, or a related field.
  • A minimum of 7 years of experience in process engineering within the pharmaceutical or biopharmaceutical industry.
  • Strong knowledge of cGMP, FDA regulations, and other relevant industry standards.
  • Proven experience in process design, scale-up, validation, and optimization.
  • Excellent analytical and problem-solving skills, with a data-driven approach.
  • Proficiency in process simulation software (e.g., Aspen Plus, HYSYS) is highly desirable.
  • Strong understanding of unit operations common in pharmaceutical manufacturing (e.g., filtration, crystallization, drying, fermentation).
  • Excellent written and verbal communication skills, with the ability to document technical information clearly and concisely.
  • Ability to work independently and collaboratively in a remote team environment.
  • Experience with Lean Manufacturing or Six Sigma methodologies is a plus.
This is an exceptional opportunity to leverage your expertise in process engineering to make a significant contribution to the development and production of life-saving medicines. If you are a dedicated and innovative engineer passionate about advancing pharmaceutical manufacturing, we encourage you to apply.
This advertiser has chosen not to accept applicants from your region.

Senior Process Engineer - Pharmaceutical Manufacturing

302012 Jaipur, Rajasthan ₹1800000 Annually WhatJobs

Posted 3 days ago

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Job Description

full-time
Our client, a leading manufacturer of high-quality pharmaceuticals, is seeking a Senior Process Engineer to optimize and enhance their production operations. This role is crucial for ensuring efficiency, quality, and compliance within the manufacturing environment. The ideal candidate will possess a strong understanding of chemical engineering principles, process validation, and Good Manufacturing Practices (GMP). This position requires a dedicated professional to be present on-site to oversee and implement process improvements.

Key Responsibilities:
  • Lead the design, development, and implementation of new manufacturing processes and the optimization of existing ones.
  • Conduct detailed process analysis, identify bottlenecks, and develop solutions to improve yield, efficiency, and product quality.
  • Develop and execute process validation protocols, ensuring compliance with regulatory requirements (e.g., FDA, EMA).
  • Troubleshoot and resolve complex process-related issues, ensuring minimal disruption to production schedules.
  • Collaborate with cross-functional teams, including Quality Assurance, R&D, and Operations, to support process development and scale-up activities.
  • Prepare technical documentation, including process flow diagrams, P&IDs, and standard operating procedures (SOPs).
  • Stay updated on industry best practices, new technologies, and regulatory changes relevant to pharmaceutical manufacturing.
  • Provide technical training and mentorship to junior engineers and operators.
  • Ensure all processes adhere to safety standards and environmental regulations.
Qualifications:
  • Bachelor's or Master's degree in Chemical Engineering or a related engineering discipline.
  • Minimum of 7 years of experience in process engineering, preferably within the pharmaceutical or biotech industry.
  • Proven experience with process design, scale-up, validation, and troubleshooting in a GMP environment.
  • In-depth knowledge of relevant manufacturing technologies and equipment (e.g., reactors, filtration systems, drying equipment).
  • Strong understanding of regulatory requirements and quality systems in the pharmaceutical industry.
  • Excellent analytical, problem-solving, and decision-making skills.
  • Proficiency in process simulation software and data analysis tools.
  • Strong project management skills and the ability to manage multiple priorities.
  • Effective communication and interpersonal skills, with the ability to collaborate effectively with diverse teams.
This is a key role within our client's manufacturing division, offering the opportunity to significantly impact product quality and operational excellence. Join our team at our state-of-the-art facility located in Jaipur, Rajasthan, IN , and contribute to the production of life-saving medicines.
This advertiser has chosen not to accept applicants from your region.
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Senior Process Engineer - Pharmaceutical Manufacturing

682001 Kochi, Kerala ₹130000 Annually WhatJobs

Posted 7 days ago

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full-time
Our client is seeking a highly experienced Senior Process Engineer with a strong background in pharmaceutical manufacturing to join their team in a fully remote capacity. This role is critical for optimizing and innovating the manufacturing processes of pharmaceutical products, ensuring compliance with stringent regulatory standards (e.g., cGMP). You will be responsible for designing, developing, and scaling up new manufacturing processes, as well as improving existing ones to enhance efficiency, yield, and quality. Your expertise will involve leveraging process simulation software, conducting root cause analysis for deviations, and collaborating with cross-functional teams including R&D, Quality Assurance, and Operations. The ideal candidate will possess deep knowledge of pharmaceutical unit operations, a strong understanding of validation principles, and the ability to drive continuous improvement initiatives in a virtual setting.

Responsibilities:
  • Design, develop, and optimize chemical and physical processes for pharmaceutical manufacturing, ensuring scalability and robustness.
  • Analyze manufacturing data to identify areas for process improvement, cost reduction, and efficiency gains.
  • Develop process flow diagrams (PFDs), piping and instrumentation diagrams (P&IDs), and equipment specifications.
  • Conduct process hazard analyses (PHAs) and implement necessary safety measures.
  • Lead validation activities for new and modified processes, including IQ, OQ, and PQ protocols.
  • Troubleshoot process deviations and implement effective corrective and preventive actions (CAPAs).
  • Collaborate with R&D and engineering teams to ensure seamless technology transfer from laboratory to commercial scale.
  • Stay current with advancements in pharmaceutical manufacturing technologies, process analytical technology (PAT), and regulatory guidelines.
  • Prepare technical reports, documentation, and presentations for internal stakeholders and regulatory submissions.
  • Mentor junior process engineers and provide technical guidance.

Qualifications:
  • Master's degree or Ph.D. in Chemical Engineering or a related discipline.
  • Minimum of 7 years of experience in process engineering within the pharmaceutical or biopharmaceutical industry.
  • In-depth knowledge of cGMP regulations and pharmaceutical manufacturing best practices.
  • Proven experience with process design, scale-up, and validation of pharmaceutical manufacturing processes.
  • Proficiency in process simulation software (e.g., Aspen Plus, HYSYS) and statistical analysis tools.
  • Strong understanding of unit operations relevant to drug substance and drug product manufacturing.
  • Excellent analytical, problem-solving, and critical thinking skills.
  • Effective communication and interpersonal skills, with the ability to lead and influence cross-functional teams remotely.
  • Experience with project management methodologies.
  • Professional Engineer (PE) certification is a plus.
This is a significant opportunity for a seasoned Process Engineer to drive innovation and operational excellence in pharmaceutical manufacturing from a remote location, impacting product quality and market availability.
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Senior Process Engineer - Pharmaceutical Manufacturing

248001 Dehradun, Uttarakhand ₹1500000 Annually WhatJobs

Posted 9 days ago

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Job Description

full-time
We are seeking a highly experienced Senior Process Engineer to join our innovative, remote-first manufacturing team. This critical role involves optimizing and developing manufacturing processes for our pharmaceutical products. You will leverage your expertise in chemical engineering, process design, and validation to improve efficiency, quality, and safety across our production lines. As a fully remote employee, you will collaborate closely with on-site teams, R&D, and quality assurance departments to implement best practices and drive continuous improvement initiatives. Your work will directly impact our ability to deliver high-quality pharmaceuticals to market efficiently and safely.

Key Responsibilities:
  • Design, develop, and optimize manufacturing processes for pharmaceutical production.
  • Conduct process simulations and analyses to identify areas for improvement.
  • Develop and implement process validation strategies and protocols (IQ, OQ, PQ).
  • Troubleshoot and resolve complex process-related issues in manufacturing.
  • Ensure compliance with Good Manufacturing Practices (GMP) and other regulatory requirements.
  • Collaborate with cross-functional teams, including R&D, QA/QC, and operations, to support product development and scale-up.
  • Develop standard operating procedures (SOPs) and training materials for manufacturing processes.
  • Manage process improvement projects from conception to implementation.
  • Evaluate and recommend new technologies and equipment to enhance manufacturing capabilities.
  • Analyze production data to monitor process performance and identify trends.
  • Contribute to capital expenditure requests and equipment specifications.

Qualifications:
  • Bachelor's or Master's degree in Chemical Engineering, Pharmaceutical Engineering, or a related discipline.
  • Minimum of 6 years of experience in process engineering within the pharmaceutical or biotechnology industry.
  • Proven experience in process design, optimization, scale-up, and validation.
  • Strong understanding of GMP, FDA regulations, and other relevant industry standards.
  • Proficiency in process simulation software (e.g., Aspen Plus) and statistical analysis tools.
  • Excellent problem-solving, analytical, and critical thinking skills.
  • Strong project management and organizational abilities.
  • Effective communication and interpersonal skills, with the ability to collaborate across different departments and in a remote setting.
  • Experience with sterile manufacturing processes is a plus.
  • Familiarity with process analytical technology (PAT) is desirable.

This is an outstanding opportunity for a dedicated Senior Process Engineer to contribute to a leading pharmaceutical company, driving innovation and excellence in manufacturing, all within a flexible remote work environment. Apply today to make a significant impact on global health.
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Senior Process Engineer - Pharmaceutical Manufacturing

160001 Chandigarh, Chandigarh ₹1100000 Annually WhatJobs

Posted 10 days ago

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full-time
Our client is a leading pharmaceutical manufacturer committed to producing high-quality medicines. We are seeking an experienced Senior Process Engineer to join our dynamic team, contributing to process design, optimization, and validation in our **Chandigarh, Chandigarh, IN** facility. This role operates on a hybrid model, blending essential on-site work with remote flexibility. You will be responsible for ensuring our manufacturing processes are efficient, safe, and compliant with regulatory standards. Your expertise in chemical engineering principles and process technology will be vital in driving operational excellence and supporting the scale-up of new products.

Responsibilities:
  • Design, develop, and optimize chemical processes for pharmaceutical manufacturing.
  • Conduct process hazard analyses (PHAs) and implement safety measures.
  • Develop and execute validation protocols for new and modified equipment and processes.
  • Troubleshoot and resolve process-related issues during manufacturing.
  • Collaborate with R&D, quality assurance, and production teams to ensure seamless technology transfer and scale-up.
  • Monitor process performance and identify opportunities for continuous improvement using statistical process control (SPC) and other methodologies.
  • Ensure compliance with Good Manufacturing Practices (GMP) and other regulatory requirements.
  • Prepare technical reports, specifications, and operating procedures.
  • Provide technical guidance and mentorship to junior engineers.
  • Evaluate and recommend new process technologies and equipment.
Qualifications:
  • Bachelor's or Master's degree in Chemical Engineering or a related discipline.
  • 7+ years of experience in process engineering, preferably within the pharmaceutical or fine chemical industry.
  • In-depth knowledge of chemical process design, scale-up, and optimization.
  • Experience with GMP regulations and validation principles.
  • Proficiency in process simulation software (e.g., Aspen Plus, HYSYS) is desirable.
  • Strong understanding of reaction kinetics, thermodynamics, and mass transfer.
  • Excellent problem-solving and analytical skills.
  • Strong project management and communication skills.
  • Ability to work effectively in a hybrid work environment and collaborate with cross-functional teams.
  • Experience with specific unit operations common in pharmaceutical manufacturing (e.g., filtration, drying, crystallization) is a plus.
This role offers a significant opportunity to contribute to the advancement of life-saving medications and to grow your career within a reputable organization. Our client is dedicated to fostering a safe and inclusive work environment where innovation thrives.
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