1,730 Pharmaceutical Field jobs in India

• Analyze, design, and optimize manufacturing processes for pharmaceutical products, ensuring compliance with GMP and other regulatory standards.
• Lead process development and scale-up activities, transitioning products from laboratory to commercial scale.
• Develop process validation strategies and protocols, and oversee execution of validation studies.
• Troubleshoot and resolve manufacturing process issues, implementing corrective and preventative actions (CAPA).
• Conduct feasibility studies and techno-economic assessments for new manufacturing technologies and process improvements.
• Prepare detailed process documentation, including P&IDs, mass and energy balances, equipment specifications, and standard operating procedures (SOPs).
• Collaborate with cross-functional teams, including R&D, quality assurance, manufacturing, and engineering, to ensure successful project outcomes.
• Stay current with industry trends, emerging technologies, and best practices in pharmaceutical manufacturing and process engineering.
• Mentor junior engineers and contribute to the development of engineering best practices within the organization.
• Manage external consultants and vendors involved in process design and implementation.

• Master's or Ph.D. in Chemical Engineering, Pharmaceutical Engineering, or a related discipline.
• A minimum of 7 years of experience in process engineering within the pharmaceutical or biotechnology industry.
• Proven experience in process development, scale-up, and validation of sterile injectables, solid dosage forms, or biologics.
• In-depth knowledge of Good Manufacturing Practices (GMP) and regulatory requirements (FDA, EMA).
• Strong understanding of unit operations relevant to pharmaceutical manufacturing (e.g., filtration, lyophilization, chromatography, granulation, tablet compression).
• Proficiency in process simulation software (e.g., Aspen Plus) and statistical analysis tools.
• Excellent problem-solving, analytical, and critical thinking skills.
• Strong project management skills and ability to manage multiple projects simultaneously.
• Excellent written and verbal communication skills, with the ability to present technical information to diverse audiences.
• Demonstrated ability to work effectively in a remote, collaborative team environment.

• Design, develop, and implement new chemical processes or improve existing ones for pharmaceutical manufacturing.
• Conduct feasibility studies, pilot plant trials, and scale-up operations for chemical processes.
• Optimize process parameters to enhance yield, purity, safety, and reduce costs.
• Troubleshoot process-related issues and implement corrective actions to maintain product quality and operational efficiency.
• Develop and maintain process documentation, including P&IDs, operating procedures, and batch records.
• Ensure compliance with all relevant regulatory requirements, including GMP, FDA, and environmental standards.
• Collaborate with R&D, production, quality control, and maintenance teams to achieve project goals.
• Perform process hazard analyses (PHAs) and implement necessary safety measures.
• Evaluate and recommend new equipment and technologies for process improvement.
• Provide technical support and training to plant operations personnel.

• Bachelor's or Master's degree in Chemical Engineering or a related discipline.
• Minimum of 5-8 years of experience in process engineering, preferably within the pharmaceutical or fine chemical industry.
• Proven experience in process design, scale-up, optimization, and troubleshooting.
• Strong understanding of chemical reaction engineering, thermodynamics, fluid mechanics, and separation processes.
• Familiarity with Good Manufacturing Practices (GMP) and regulatory requirements for pharmaceutical production.
• Experience with process simulation software (e.g., Aspen Plus, HYSYS) is highly desirable.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong communication and interpersonal skills, with the ability to work effectively in a multidisciplinary team.
• Proficiency in technical documentation and report writing.
• Commitment to safety, quality, and continuous improvement.

• Lead the design, optimization, and validation of pharmaceutical manufacturing processes.
• Ensure compliance with cGMP and other relevant regulatory requirements.
• Troubleshoot and resolve process-related issues to maintain operational efficiency.
• Drive continuous improvement initiatives to enhance product quality and reduce costs.
• Collaborate with R&D, QA, and Operations teams on process development and scale-up.
• Manage process transfer projects and implement new manufacturing technologies.
• Mentor and guide junior process engineers.

• Bachelor's or Master's degree in Chemical Engineering or a related field.
• Minimum 7 years of experience in process engineering within the pharmaceutical or biopharmaceutical industry.
• Proven expertise in process validation, scale-up, and optimization.
• Strong knowledge of cGMP regulations and pharmaceutical manufacturing standards.
• Proficiency in process simulation software and statistical analysis tools (SPC, DoE).
• Excellent leadership, communication, and project management skills.
• Experience with Lean manufacturing principles is a plus.

• Analyze existing manufacturing processes to identify areas for improvement in efficiency, yield, and cost-effectiveness.
• Design, develop, and implement new manufacturing processes and technologies, ensuring scalability and robustness.
• Oversee process validation activities, including IQ, OQ, and PQ, in accordance with regulatory guidelines.
• Troubleshoot and resolve process-related issues, performing root cause analysis and implementing corrective actions.
• Develop and maintain process documentation, including SOPs, batch records, and engineering drawings.
• Collaborate with R&D, Quality Assurance, and production teams to ensure seamless process transfer and execution.
• Monitor key process parameters and implement statistical process control (SPC) measures.
• Ensure all processes comply with cGMP, FDA, and other relevant regulatory requirements.
• Provide technical leadership and mentorship to junior engineers and technical staff.
• Stay updated on industry best practices, emerging technologies, and regulatory changes in pharmaceutical manufacturing.

• Bachelor's or Master's degree in Chemical Engineering, Mechanical Engineering, or a related discipline.
• Minimum of 6 years of relevant experience in process engineering within the pharmaceutical or biopharmaceutical industry.
• Strong knowledge of pharmaceutical manufacturing processes, including API synthesis, formulation, and sterile manufacturing.
• Proficiency in process simulation and modeling software.
• Experience with process validation, qualification, and regulatory compliance (cGMP, FDA).
• Excellent analytical, problem-solving, and critical-thinking skills.
• Strong understanding of equipment used in pharmaceutical manufacturing.
• Exceptional communication and interpersonal skills, with the ability to collaborate effectively across remote teams.
• Project management experience is highly desirable.
• Knowledge of Lean Manufacturing or Six Sigma methodologies is a plus.

• Analyze existing manufacturing processes to identify areas for improvement in efficiency, yield, and cost reduction.
• Design, implement, and validate new process technologies and equipment.
• Troubleshoot process deviations and equipment malfunctions, providing timely and effective solutions.
• Develop and maintain Standard Operating Procedures (SOPs) and batch records.
• Ensure all processes comply with Good Manufacturing Practices (GMP) and relevant regulatory requirements (e.g., FDA, EMA).
• Conduct process hazard analyses (PHAs) and implement safety measures.
• Manage process validation activities, including protocol development, execution, and reporting.
• Collaborate with R&D, Quality Assurance, and Operations teams to support product development and lifecycle management.
• Train and mentor junior engineers and operational staff on process operations and best practices.
• Monitor key process performance indicators (KPIs) and generate reports for management.
• Lead or participate in cross-functional teams for process optimization projects.

• Bachelor's or Master's degree in Chemical Engineering, Industrial Engineering, or a related discipline.
• Minimum of 6 years of experience in process engineering within the pharmaceutical or biotechnology industry.
• Proven expertise in process optimization, scale-up, and validation.
• Strong understanding of GMP regulations and pharmaceutical manufacturing principles.
• Proficiency in process simulation and modeling software (e.g., Aspen Plus, HYSYS) is a plus.
• Excellent analytical, problem-solving, and critical-thinking skills.
• Strong project management skills and the ability to manage multiple tasks simultaneously.
• Effective communication and interpersonal skills, with the ability to collaborate across departments.
• Experience with aseptic processing, sterile manufacturing, or biologics is highly desirable.
• Ability to adapt to a hybrid work environment, balancing remote responsibilities with on-site operational needs.

• Develop, optimize, and scale-up chemical synthesis routes for APIs and intermediates.
• Design and conduct laboratory experiments to study reaction mechanisms and kinetics.
• Identify and control critical process parameters to ensure robustness and reproducibility.
• Troubleshoot and resolve issues in existing chemical manufacturing processes.
• Improve process efficiency, yield, purity, and safety.
• Collaborate with analytical chemists to develop and validate analytical methods.
• Prepare detailed technical reports, protocols, and process validation documents.
• Ensure compliance with Good Manufacturing Practices (GMP) and relevant regulatory guidelines.
• Transfer developed processes from laboratory scale to pilot and commercial scale.
• Conduct process hazard analyses and implement safety measures.
• Stay current with advancements in synthetic organic chemistry and process development technologies.

• Ph.D. or Master's degree in Organic Chemistry, Chemical Engineering, or a related field.
• Minimum of 7 years of experience in process chemistry, preferably within the pharmaceutical industry.
• Proven track record in developing and scaling up complex chemical syntheses.
• Strong knowledge of organic reaction mechanisms, process optimization techniques, and scale-up principles.
• Experience working in a GMP-compliant environment.
• Proficiency in analytical techniques such as HPLC, GC, NMR, and Mass Spectrometry.
• Excellent problem-solving, analytical, and experimental design skills.
• Strong written and verbal communication skills, with the ability to document scientific findings clearly.
• Ability to work effectively in a collaborative team environment, as well as independently.

• Design, develop, and optimize chemical and pharmaceutical manufacturing processes to improve yield, efficiency, and quality.
• Lead the scale-up of laboratory processes to commercial manufacturing, ensuring robust and reproducible results.
• Develop and implement process validation strategies and protocols in compliance with regulatory requirements (e.g., FDA, EMA).
• Troubleshoot and resolve complex process-related issues, identifying root causes and implementing effective corrective actions.
• Collaborate with R&D, Quality Assurance, and Production teams to ensure seamless integration of new processes and technologies.
• Develop Standard Operating Procedures (SOPs) and batch records for manufacturing processes.
• Conduct process hazard analyses (PHAs) and implement safety measures to ensure a safe working environment.
• Utilize process simulation software and data analysis tools to model and predict process performance.
• Stay current with industry trends, new technologies, and regulatory changes in pharmaceutical manufacturing.
• Mentor and guide junior engineers, fostering a culture of continuous improvement and technical excellence.
• Manage process improvement projects, including defining scope, objectives, and timelines.
• Prepare technical reports, documentation, and presentations for internal stakeholders and regulatory submissions.
• Ensure compliance with all GMP, safety, and environmental regulations.
• Evaluate and recommend new equipment and technologies to enhance manufacturing capabilities.
• Optimize existing processes for cost reduction and waste minimization.

• Bachelor's or Master's degree in Chemical Engineering, Pharmaceutical Engineering, or a closely related field.
• Minimum of 7 years of experience in process engineering within the pharmaceutical or biopharmaceutical industry.
• Strong understanding of GMP, FDA, and other relevant regulatory guidelines.
• Proven experience in process design, scale-up, optimization, and validation.
• Proficiency in process simulation software (e.g., Aspen Plus, CHEMCAD) and statistical analysis tools.
• Excellent analytical, problem-solving, and project management skills.
• Demonstrated ability to lead projects and mentor junior team members.
• Strong communication and interpersonal skills, essential for remote collaboration.
• Experience with process analytical technology (PAT) is a plus.
• Knowledge of sterile manufacturing processes is advantageous.
• Ability to work independently and manage multiple priorities effectively in a remote setting.

Pharmaceutical Manufacturing Operator / Line Setter

• South East Melbourne
• Permanent role
• Afternoon and Night Shift

Seeking motivated Line Setters with minimum 2-3 years’ experience, preferably in pharmaceutical or food industry for afternoon and night shift. Do not miss an opportunity to be part of a growing, innovative Australian owned Pharmaceutical company based in South East Melbourne!

Key Responsibilities:

• Ensure that the line runs efficiently and productively; coordinate tasks so that the line runs as continuously as possible
• Troubleshoot and adjust equipment during the run to achieve optimum output and minimal down time minimise wastage
• Set up filling and packing equipment and strip down, wash and reassemble filling equipment to produce a quality product as efficiently as possible
• Monitor the quality of product throughout the filling run and make appropriate adjustments to maintain quality and compliance
• Be able to operate and maintain equipment safely and change parts in a clean and orderly manner
• Ensure that all work is done according to the highest standards of Good Manufacturing Practice (GMP)
• Carry out required tasks in SAP and other systems; complete all relevant documentation and reporting
• Participate in required training, including SOPs, GMP, OH&S and 5S

Key Requirements:

• Written and oral communication skills
• High mechanical aptitude
• Troubleshooting and problem solving skills
• Advanced GMP and sound understanding of OHS
• Proactive, self-motivated and ability to work unsupervised
• Proven machine operating experience in either food manufacturing or pharmaceutical

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IMPORTANT: It is a requirement of all our jobs that you have a PR or AU/NZ Citizenship. A work visa is not sufficient as all our jobs are permanent. Please do not apply if you do not meet these requirements.

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