Introduction:
Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S. Bhartia and Mr. Hari S. Bhartia with strong presence in diverse sectors like Pharmaceuticals, Life Science Ingredients, Contract Research & Development Services, Therapeutics, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Group has global presence employing around 42,000 people across the globe with over 2,400 in North America.
Jubilant Pharmova Limited
Jubilant Biosys Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radiopharma, Allergy Immunotherapy, CDMO Sterile Injectables, Contract Research Development and Manufacturing Organisation (CRDMO), Generics and Proprietary Novel Drugs businesses.In the Radiopharma business, the Company is involved in manufacturing and supply of Radiopharmaceuticals with a network of 46 radio-pharmacies in the US. The Company’s Allergy Immunotherapy business is involved in the manufacturing and supply of allergic extracts and venom products in the US and in some other markets such as Canada, Europe and Australia. Jubilant through its CDMO Sterile Injectables business offers manufacturing services including sterile fill and finish injectables (both liquid and lyophilization), full-service ophthalmic offer (liquids, ointments & creams) and ampoules.The CRDMO business of the Company includes the Drug Discovery Services business that provides contract research and development services through two world-class research centres in Bangalore and Noida in India and the CDMO-API business that is involved in the manufacturing of Active Pharmaceutical Ingredients. Jubilant Therapeutics is involved in Proprietary Novel Drugs business and is an innovative biopharmaceutical company developing breakthrough therapies in the area of oncology and autoimmune disorders. The company operates six manufacturing facilities that cater to all the regulated market including USA, Europe and other geographies.Find out more about us at www.jubilantpharmova.com .
The Position
Organization-
Jubilant Biosys Limited
Designation –
Manager – Technology Transfer
Location-
Nanjangud, Mysore
Shall be responsible for the following activities:
- Preparation of RFP , PFD equipment mapping for CDMO projects, Hands on experience in handling CDMO project , Planning scheduling and execution in plant.
- Review the R&D process & Synthetic Scheme and to evaluate the process with respect to operability, engineering aspects, environment & safety aspects of handling new chemicals, New Unit Processes/operations with commercial scale-up point of view.
- Prepare & share the what-if for the proposed process with the R&D for data generation purpose and to review the available data.
- Select the appropriate batch size for scale-up in pilot/commercial plant & prepare PFD, mass balance for the proposed process, RM list for indenting purpose, Modification list and P&ID (Wherever applicable). Conduct the HAZOP study with cross functional teams involving Safety, manufacturing, R&D, Engineering services and to prepare the HAZOP report and implement the recommendations from HAZOP study.
- Conduct & observe the demo batches in R&D lab for absorbing the technology for all critical unit process & unit operations and evaluate the process with respect to operability in Plant.
- Review the BPR prepared for trials & validations and incorporate the learnings from lab batches, HAZOP recommendations.
- Monitor the batches adequately during trial and validations in pilot plant or in commercial plants.
- Prepare the scale-up report and capture all the learning’s observed during the trial batch.
- Generate/capture adequate data during lab and Pilot batches ensuring smooth commercialization.
- Investigate the failures during the trial and validation batches (Whichever suitable) and implement the corrective and preventive actions.
- Prepare the disposal plan and analysis data for the effluents generated during the process.
- Keep the record of plan V/s actual with respect to deliverables, timelines, process and cost efficiencies.
Responsible for the following activities:
- Keep a record of deviations and CCF’s for the concerned products and ensure closure of CCF’s and deviations.
- Track-wise responsibility for initiation, review, reject and SME approval, to support the manufacturing department
- Electronics Document management system (EDMS) responsibility for preparation, review, reject and SME approval, to support the manufacturing department.
- Provide training to the concerned production personnel on the process criticalities and for handling of the raw materials, intermediates, API’s safely.
- Coordinate with project management, business teams for the respective products and keep them informed on the progress of the project.
- Conduct the pre-validation meetings based on the experimental batch outcome and preparation of MOM.
- Prepare all critical relevant data collection and compilation.
- Coordinate for approval of genotoxic risk assessment.
- Performing any other activity assigned by immediate supervisor as and when required.
- Responsible to conduct experiments (Performance, trouble shooting, etc..) at R&D and updating the respective lab note book.
Person Profile.
Education Qualification: B.Tech / M.Tech Chemical Engineering
Experience Range
: 10+ years
Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances.
To know more about us, Please visit our LinkedIn Page-
https://www.linkedin.com/company/jubilantpharmova/mycompany/
