Piramal Enterprises is Hiring for Research Scientist ,Apprentice,Research Associate,Executive QA ,Senior Research Associate and has issued notification to accept Applications.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. A global leader in integrated solutions, it offers a comprehensive range of services across the drug life cycle from drug discovery services and development to commercial manufacturing of drug substances and drug products. With accreditations from regulatory bodies in the US, Europe & Japan, its development centres and manufacturing sites across the globe, committed to research and development programs.. Interested and eligible candidates required to fill application form in online with Education and personal details and submit application along with resume .Job application form link provided at the end of post. Eligibility for the Research Scientist ,Apprentice,Research Associate,Executive QA ,Senior Research Associate as follows.
Vacancy summary details :
- Company Name: Piramal Enterprises
- Location : India-GUJARAT,MADHYA PRADESH
- Post Name: Research Scientist ,Apprentice,Research Associate,Executive QA ,Senior Research Associate
- Qualification: B.Pharma, M.Pharma, M.sc
- No of Vacancies: NA
- Details of Salary: NA
- Closing date for online Application : Apply as soon as possible
- Mode of application : online
- Selection Process: Shortlisted candidates may called for selection process (Â Personal interview , Group discussion , etc…,)
Job Description/Skills Required:Â
- Literature and patent evaluation (PAR, FOI, reviews, articles)
- Defining product development strategy
- Formulation development, optimization, scale-up and technology transfer of generic and new chemical entity projects.
- Formulation development by QbD principles to ensure the quality, efficacy and safety of product
- Preparation and/or review of technical documents like product development reports, batch records and technology transfer documents.
- Good Communication skills
- Extending cooperation to support team for smooth functioning of project
- Exposure to IQ, OQ and PQ process.
- Trouble shooting of high impurity level, dissolution matching (discriminatory media)
- Bio results interpretation
Job Description:
* LC-MS/HPLC Method Development
* Analytical Method Development of newly developed products independently.
* Interpretation of IR & NMR Spectra.
* Isolation and characterization of Impurities.
* Responsible for troubleshooting of instruments in case of problems.
* Impurity Profiling of Drug substances.
* Calibration of Analytical Instruments.
* HPLC (Shimadzu Technology)
* PHÂ meter
Job Description
- To assure & review quality system and to ensure the compliance with established standards.
- Ensure effective implementation of systems and procedures as per cGMP, GLP, ISO 13485 and other regulatory/customer requirements.
- Participate in risk assessment, provide risk-assessment tracking and other established mechanisms for risk assessment.
- Handling of various QMS related software’s like TrackWise, ENSUR and SAP.
- To represent QA department in external and internal audits including their compliance and responding to audit observations, customer queries related to QA and to ensure appropriate corrective actions based in audit findings.
- Participate in Quality Improvement Projects and their implementation.
- Handling of documentation related to self-inspection and to maintain the same as per procedure.
- Develop reports and analyses to document potential risks and gaps that need corrective action or preventative action.
- To impart training to team members/other concerned personnel/new employees on SOP’s and on job training.
- To update on regulatory requirement and implementation.
- To initiate change control for changes in documents as per requirements. Participate in review of Change Controls.
- To Review and Approve QMS like Deviation, Investigations, Change Control etc.
- To participate in the investigation of complaints related to quality of products.
- Site champion for QuEST. Assist in preparation and sharing MIS, QIP etc. with site senior team, corporate team and / or customer on timely basis.
- Monthly assessment of Warning letter, 483s and other regulatory observations within industry.
- Support to site DICO (Data Integrity Compliance Officer) for monitoring and implementation of actions related to Data Integrity awareness at site.
- To ensure the EHS (Environment, Health and Safety) related activities to be completed on time and to support EHS activities as per requirement. To report near miss and incidences as observed as per EHS requirement.
- To ensure data integrity compliances at site and while performing activities.
Job Description:
* LC-MS/HPLC Method Development
* Analytical Method Development of newly developed products independently.
* Interpretation of IR & NMR Spectra.
* Isolation and characterization of Impurities.
* Responsible for troubleshooting of instruments in case of problems.
* Impurity Profiling of Drug substances.
* Calibration of Analytical Instruments.
* HPLC (Shimadzu Technology)
* PHÂ meter
How to Apply :
Step 1: Click on below link and you will be redirected to Career Page of Recruiting Company or Career portal.
Step 2. Register on Career Page of the Company or Career Portal by giving log in credentials and other personal or education details .
Step 3.Upon successful registration .User need to log in with credentials.
Step 4.Once logged in, User need to fill the all relevant personal ,educational , Work experience details ,attach resume and submit application form.
Click here for notification and Apply
