Piramal Released Job Openings On 02/02/2022.Piramal Enterprises Limited is the Contract Development and Manufacturing Organisation (CDMO) business division of Piramal Enterprises Limited, with operations in North America, Europe and Asia.Â
Vacancy Details:
Piramal Recruiting M.Sc/M.Pharm Graduates with 01+ Years of Experience for Research Scientist/Senior Research Associate/Senior DevOps Engineer/Senior Analyst/Senior Associate Principal/Manager – Packaging Development/Area Business Manager/Manager – Pilot Plant Position.
Important Details :
- Location : India-GUJARAT/India-Karnataka/India-Maharashtra/India-Tamil Nadu
- No of Vacancies:NA
- Details of Salary:NA
- Opening date for online Application: 02/02/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
Related Job : B.Pharm,M.Pharm,B.Sc,M.Sc Graduates Latest Openings
Job Description/Skills Required
Senior Research AssociateÂ
- To perform calibration of the analytical instruments as per calibration schedule under supervision of Manager
- Follow the standard practices- CGLP during Lab experiments.
- To get trained on Maintain hygienic condition in respective department.
- To get trained on Cleaning verification method development and Validation
- To get trained on API method evaluation and verification.
- Following in-house compliance system.
- To get trained on Method development for drug product formulation
- Learn Routine analysis of development samples and lab stability samples under supervision of Manager
- Preparation of test procedures for routine development analysis under supervision of Manager
Research ScientistÂ
- To perform calibration of the analytical instruments as per calibration schedule under supervision of Manager
- Follow the standard practices- CGLP during Lab experiments.
- To get trained on Maintain hygienic condition in respective department.
- To get trained on Cleaning verification method development and Validation
- To get trained on API method evaluation and verification.
- Following in-house compliance system.
- To get trained on Method development for drug product formulation
- Learn Routine analysis of development samples and lab stability samples under supervision of Manager
- Preparation of test procedures for routine development analysis under supervision of Manager
Senior Principal ScientistÂ
- Preparation of formulation development strategy for client projects, its execution and tech transfer (virtually / with physical presence)
- Leading team of formulation development scientists and providing technical expertise
- Ensuring consistent on-job trainings during project experimentations and reviews
- Leading project related teleconferences with clients on technical
- Regular feedback to client through telecom / email on project progress
- Reviewing RFQs and preparing proposals for new projects
- Ensure smooth day to day project related activities in pilot plant and formulation development lab
- Ensuring GLP in lab and GMP in pilot plant and supporting quality audits
- Ensuring the completion of project within agreed timeline, cost, specs
- Fulfil primary and secondary customer requirements with respect to EHS and QA issues and other legal regulatory compliance
- Review of project related documents like, development protocols, reports, packaging and manufacturing records etc. for good technical writing and adequacy
- Performance review (half yearly / annually) of team members
- Coordination and integration with all on-site / off-site functions toward on-time delivery of the projects
- Supporting leadership in various organizational / site initiatives
- Providing project updates to line managers and Person in Plant (PIP) of client on regular basis
- Ensuring strong integration of team members with cross-functions for on-time project deliverables
- Ensure compliance and awareness of data integrity at functional area and site.
- Follow GxP (GMP, GDP etc.) for all processes and train the subordinates to follow the same
- To perform cross-functional internal audits at site
EXECUTIVE QC
•To handle LCMS Shimadzu 8040 Triple QUADRUPOLE Mass Spectrometer,
•To provide ES-MS, MS/MS, LC-MS and LC-MS/MS support to NDD, API and formulation department.
•LC-MS method development for New Chemical Entity (NCE), API and Finished Products Impurity identification by LC-MS and LC-MS/MS
•Finished Organic intermediates were precisely identified (LCMS, NMR & IR) and analyzed using various analytical Instruments – LC-MS, HPLC, FT-IR, GC, GC-HS, UV-Visible etc.
•Troubleshooting of Analytical Instruments like LCMS, HPLC, GC,GCMS, GCHS etc
•Online Reaction monitoring of chemical reaction by LCMS & GC and confirm the product Formation. Mass identification by ESI & APCI ionization techniques & Trouble shooting.
Packaging Development
- Development of change parts for blister packing machine
- Development of artwork for AGILE projects.
- Innovator pack analysis and report preparation
- Preparation of BOM for RFQ for BD/PM team.
- Label Preparation for Exhibit batch Packing
- Arrangement of packing material samples for trial
- Preparation of department related SOP
- Arrangement of packing material standards/ References from suppliers for development/regulatory compliance
- Support in arrangement of test methods for PM
- Visit/Audit of PM vendors
- Support QA for qualification of new packing material
- Development of Key line drawings for customer project for AW preparation
- Preparation of BOM for commercial/Exhibit batch packing
- Review of primary/secondary/tertiary packing material specification
- Co-ordinate for new packing machine development
- Responsible for machine trial for packing component.
- Approval of print proof/shade cards for artwork development
- Preparation of MPC for R & D packing/Tech transfer for AGILE projects.
- Bar code and pharma code printing, implementation and verification.
- Development of new packaging machinery
- Dealing with customer as per project requirements
- Development of all mock up samples for Trials/Registration purpose
- Monitoring of packaging material stock for art work revision.
- Co-ordinate with various vendor for packaging material
- Attend various training programs.
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