Lupin Ltd Walk In Interview 2022.Lupin Ltd. Notification full details below.Interested and eligible candidates can Apply Now.Lupin, we are guided at all times by our promise of caring for our customers’ health and well-being. To achieve this objective, we have invested in research, continuous learning and technology to develop high quality and affordable medicines to address unmet patient needs.Science can be a potent catalyst for change and transformation. This conviction in the power of science to improve health outcomes and uplift communities served as the guiding light for our founder, Dr. Desh Bandhu Gupta, and for Lupin, the company he founded in 1968.
- Post Name: Manager/Senior Executive – QC Bioassay/Sr. Manager – Product/Manager – Product/Associate Scientist – Injectable Analytical/Research Associate – Analytical Inhalation/Research Associate – Formulation Development
- Qualification: Master’s degree in Pharmaceutics
- Experienced:A minimum of 3 years of hand-on experience in formulation development (injectables and peptides).
- Salary: Not Disclosed
Job Description: Greeting from Lupin Ltd !!!!
Important Details :
- Location: Pune/Mumbai, IN/Santacruz, MH, IN
- Post of date:14/11/2022
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face interview
- Interview Rounds of Interview: HR
Roles and Responsibilities
Senior Executive – QC Bioassay
Review and ensure periodic updating of SOP’s, STP’s and specifications pertaining to biotherapeutics
Timely testing with online documentation of various sample stages including in process, intermediate, drug substance/drug product
Stability samples of biotherapeutics proteins for test parameters including but not limited to cell based assay
Binding ELISA based assays and general procedures but not limited to mycoplasma testing
Preparation of reagents/solution required for routine testing and maintenance of their records
Participation in transfer of analytical methods from R&D to QC and review method transfer reports and raw data
To ensure stability management and timely preparation/checking of stability summary/stability closure reports
Ensure timely in-house calibration/verification of analytical equipment as per the approved procedures and calibration/verification frequency
Online monitoring and maintenance of equipment records
Coordinate with vendors for timely execution of AMC/Preventive maintenance as per defined frequency
To ensure cGMP compliance and maintain the laboratory in audit ready condition
To report any deviations/out of specifications results and safety risks to the supervisor as and when observed
To attend all GMP/On-job/additional trainings as per the approved training matrix and update the training records
You will be responsible for:
Formulation Development of Injectable Products like Solutions, Lyo Products, Suspensions and should also be familiar with advance analytical characterization studies understanding for regulated market .e.g. USA and Europe
To carry out product development trials, process optimization trials, scale up trials and exhibit batches at manufacturing plant.
Literature search of new products, conduct pre formulation studies, other studies like tubing compatibility and filter studies.
Preparation of product development protocols, QbD/ Risk Assessment documents, technology transfer documents and product development reports.
Require good oral and written communication skills.
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