Rubicon Research Pvt. Ltd Walk-in Interview 2023. Rubicon Research Pvt. Ltd Notification full details below.Interested and eligible candidates can attend interview on scheduled time and venue.Rubicon Research is an IP led, specialty pharmaceutical company focused on our mission to provide innovative yet affordable patient-centered products and solutions so as to address unmet needs around the world. We leverage our proprietary technologies and specialized formulation development skills to provide solutions to complex delivery challenges; enabling better patient outcomes.
- Post Name: Officer/Senior Officer Technology Transfer
- Education: Bpharm,Mpharm
- Experienced: 5-8 years
Job Description: Greeting from Rubicon Research Pvt. Ltd !!!!!
Important Details :
- Location:Mumbai (All Areas)( Ambernath )
- Post of date:25/05/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face
- Interview Rounds of Interview: HR
Roles and Responsibilities
Candidate should have good exposure at Technology Transfer .This Position will based in Plant.t.
1.To evaluate and to ensure the smooth transfer of technology from the transferring site to receiving site by coordinating with relevant applicable departments.
2.To perform GAP analysis / extensive review of the project / product to be introduced from 3.Transferring site to Receiving site and its status reporting to superior for further course of action.
4.Verification of new item code requests, vendor code requests, purchase requisition with respect to relevant project needs.
5.Preparation of project / product introduction related documents like Strategy, Scope, Activity plan etc.
6.Initiation, Handling and follow-up of Change control, Deviation, Investigations regarding OOS / OOT till its target completion date and to ensure its proper closing as per the specified timeline given in SOP.
7.To read and understand the Master Formula Card provided by Formulation development or the client regarding preparation / revision of Bill of Material (BOM), Batch Manufacturing Record (BMR) and Batch Packaging Record (BPR) for Clinical trial, Optimization and Exhibit / Submission batches.
8.Preparation and Revision of process optimization / evaluation / validation protocol.
9.To prepare and maintain the individual project files for better tracking and retrieval of data.
10.To give BMR / BPR request to QA for issuing the same for Clinical trial, Optimization and Exhibit / Submission batch (s) execution.
11.To monitor dispensing of RM & PM in warehouse as per relevant SOP.
12.Monitoring of Clinical Trial, Optimization and Exhibit / Submission execution and necessary support for Manufacturing in order to ensure the process, GMP, regulatory etc. compliance level.
13.To support manufacturing during initial commercial validation batches and preparation of necessary documents (whichever is applicable).
14.To raise technical information sheet to QA for the analysis of samples from respective stages of above specified batches which is to be withdrawn by QA during its process execution.
15.To adhere to cGMP and all relevant SOPs related to manufacturing / packing activity.
16.To perform / check in-process control checks for manufacturing / packing process and recording of observations in respective BMR / BPR.
17.To fill / record manufacturing / packing activity observations in respective BMR / BPR online and to fill other relevant documents pertaining to products, systems, equipments / instruments, log books etc.
18.Preparation of process optimization / evaluation / validation reports and subsequent follow up till its approval.
19.Proper status reporting regarding project / product to superior.
20.To performed the duties of HOD in his unavailability.
Desired Candidate Profile Candidate shuld have good exposure at Technology Transfer .This Position will based in Plant.
interested candidates may apply on firstname.lastname@example.org