Pharmaceutical Process engineers are involved in the planning, conception, design, construction/Execution, management, operation of research facilities, pilot plant for scale up, manufacturing plants and labeling & packaging processes in the conversion of chemical and biological materials into valuable pharmaceuticals and pharmaceutical therapies. They have to implement FDA regulations, validation assurance, quality control, and maintain Good Manufacturing Practices (GMP) compliant facilities. In addition to the safety of the end product, they have to maintain a level of personal and environmental safety. The processes that they come up with are used to create products ranging from oil, gas & drugs to food and drink.
This programme will provide a thorough understanding of Process engineering in API and in formulation for develop and design new process and modify existing ones in very cost effective way with safety, increase productivity in existing system, engineering calculations for taking decision at spot etc. This programme provides professionals with the skills and knowledge to allow them to participate effectively in the creation and growth of high impact pharmaceutical business ventures. The development of this programme is in direct response to the demands of industry and its professionals will be highly competitive in the global jobs market.
This short term programme has been designed mainly to provide brief of Pharmaceutical Process Engineering. The programme provides collecting, linking, and manipulating different types of biological information to discover new biological insight. Thus it works as re-fresher programme for those already in the industry and an insight or practical guide for those planning to enter into this sector. You can complete this programme from your own city.
Module 1: Process Engineering in the pharmaceutical industry: An Introduction
Module 2: Regulatory aspects (India & International): FDA regulations and ICH guidelines, safety aspects, Policy, Legal and statutory framework on industrial safety and health.
Module 3: Technology Transfer by Process Engineer in pharmaceutical Industry and Various Functions of departments of industry
Module 4: Stoichiometry & the Role of Chemical Engineering in Pharmaceutical API Process R & D.
Module 5: Industrial Processes for Reactions, Reactor types & Design with accessories.
Module 6: Heat and mass Transfer Operations
Module 7: Process Engineering Package & Designing with material and energy balance, Process diagrams and project costing.
Module 8: Fluid handling - Fluid flow, Line sizing, Pressure drop calculation, Pipe network analysis, Pumps & Compressor, Steam, compressed air, ETP, refrigeration & HVAC system.
Module 9: Industrial Unit Processes - Air conditioning & Humidification, Various separation process - Distillation, Evaporation, Crystallization, Filtration & Drying.
Module 10: Particle Size, Reduction and classification, Mixing
Module 11: Process Engineering role in Clean Room Management, solid dosage formulation, Sterilization and Bio-processing
Module 12: Pilot Plant - Scale up and HAZOP study
Module 13: Material packaging and quality principles.
Module 14: An Introduction to CHEMCAD
Module 15: Industry based Case Studies
Any Graduation/ B.tech/ B.Sc. in Microbiology/ Life Sciences/ Botany/ Zoology/ Food Science/ Food Technology/ BE/ B.Pharma/ MBBS/ BDS/ BHMS/ BUMS/ BAMS or any other discipline. Diploma holders are eligible for our Executive Diploma, Industry Certificate, and Certificate Programmes.
The duration to complete this programme is 1 year (Post Graduate Diploma), 6 months (Executive Diploma).
The registration dates for this programme run by the Institute are updated timely on the webpage. Effective online learning tools incorporated into the design of the webpage make the programme lectures and study material easily accessible. This gives huge window of self-regulated and self-paced performance to the participants.
A comprehensive study material for all the modules in hard copies ensuring the needs of the audience. The accompanying training material is appropriately aligned with the current Industry’s expectations.
IGMPI follows a credit system based on all learning activities involved in studying for all PG Diploma, Executive Diploma and Certificate Programmes. Each of your modules is equal to 4 credits. To successfully complete the programme, you will have to earn all the credits assigned to your programme.
All the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Post Graduate Diploma/Executive Diploma in Pharmaceutical Process Engineering by Faculty of Product Management, IGMPI. For all the above-mentioned modules, Online Classes (Online mode) or face-to-face classes (Regular mode), elaborate programme material, self-assessment assignments would be provided by the Institute. Details get updated on the webpage as well.
The Institute has partnered with many organizations for providing with placement assistance to its participants. Besides, it has a robust placement cell comprised of senior level Human Resources professionals and Talent Acquisition experts which maintains close links with business and industry. This cell is continuously engaged in promoting the employability of our participants and encouraging the concerned Human Resources department and Hiring Managers to recruit/hire our participants for their vacant positions. The efforts of our placement cell also include helping with professional resume writing & interview skills.
In recent months the Institute has witnessed more and more participation from professionals working with global healthcare like Uflex Ltd., Anuroop Packaging Ltd., IPCA, Zydus, Unichem, Sun Pharmaceuticals, Hetero, Torrent Pharmaceutical, Cipla, Lupin, Johnson & Johnson, Pfizer, Roche, Intas, Asrezenenca, Gland, Glenmark, Macleods, Jubilant Lifesciences, Novartis, Merck, Piramal, Dr. Reddy’s Laboratories, Hamdard, Lotus, Lakme, Khadi, Himalayan, Sun Pharmaceutical, Pfizer, Piramal Pharma Solutions, Novartis Pharma, IQVIA, Eli Lilly and Company, etc. The IGMPI’s Corporate Resource Division actively recommends our students and training participants for various job requirements and specialized roles to Human Resource, Talent Acquisition as well as the heads of various departments in Pharmaceutical, Healthcare industries on regular basis.
Pharmaceutical Process Engineering provides a strong focus on problem solving, Technical, conception, design as well as managerial and practical application of knowledge to particular fact scenarios through a number of advice drafting exercises. The Process Engineer professionals will execute the process development experiments and process optimization of API & formulations, Scale-up of API & formulations from lab scale to pilot/commercial scale, execution of submission batches and validation, Preparation & review of batch documents & protocols. Process Engineering is important in extending benefits of R&D, Production and engineering to the society at a large, especially in developing countries. Technology Transfer is important for commercialization especially, in the case of developing and underdeveloped countries.
Pharmaceuticals | Food | Clinical Research | Healthcare | Medical Coding | Medical Device | Nanotechnology | IPR
Featured Article
Moderated by Shri Vinod Arora, Principal Advisor, IGMPI (Building FR&D Talent in India)
Moderated by Shri Vinod Arora, Principal Advisor, IGMPI
Moderated by Shri Vinod Arora, Principal Advisor, IGMPI
Moderated by Shri Vinod Arora, Principal Advisor, IGMPI
GMP: A continous process
Fighting fakes with technology
Trends in lab design
Oral solid dosage forms: Trends and opportunities
Optimising FR&D to expedite regulatory complaince
By Shri Vinod Arora, Principal Advisor, IGMPI
Featured Article
Moderated by Shri Vinod Arora, Principal Advisor, IGMPI (Building FR&D Talent in India)
Moderated by Shri Vinod Arora, Principal Advisor, IGMPI
Moderated by Shri Vinod Arora, Principal Advisor, IGMPI
Moderated by Shri Vinod Arora, Principal Advisor, IGMPI
GMP: A continous process
Fighting fakes with technology
Trends in lab design
Oral solid dosage forms: Trends and opportunities
Optimising FR&D to expedite regulatory complaince
By Shri Vinod Arora, Principal Advisor, IGMPI
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