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Post : Senior Research Associate - AD

Job Description
1. Analytical method development and validation of different types of dosage forms (Tablet, Capsules) with protocol and report preparation.
2. Routine/stability analysis of formulation development samples
3. Documents review
4. Training to new joiners
5. Interact and coordinate with senior for day to day work allocation
6. Communication with supplier / vendors for Instrument maintenance and columns / chemicals inquiry.
7. Attend telecon for client communication
8. Follow the standard practices, cGLP/cGMP during lab experiments.
9. To perform calibration of the analytical instruments as per calibration schedule.

Additional Information
Qualification : M.Sc in Analytical / M.Pharm
Location : Ahmedabad  Plot No:-19,PHARMEZ, Sarkhej-Bawala NH-8A Village Matoda Tal-Sanand  Ahmedabad 382213
Industry Type : Pharma
Functional Area : R&D
End Date : 30th April, 2019

Require Senior Research Associate at Piramal Enterprises @ APply Now

Post : Senior Research Associate - AD

Job Description
1. Analytical method development and validation of different types of dosage forms (Tablet, Capsules) with protocol and report preparation.
2. Routine/stability analysis of formulation development samples
3. Documents review
4. Training to new joiners
5. Interact and coordinate with senior for day to day work allocation
6. Communication with supplier / vendors for Instrument maintenance and columns / chemicals inquiry.
7. Attend telecon for client communication
8. Follow the standard practices, cGLP/cGMP during lab experiments.
9. To perform calibration of the analytical instruments as per calibration schedule.

Additional Information
Qualification : M.Sc in Analytical / M.Pharm
Location : Ahmedabad  Plot No:-19,PHARMEZ, Sarkhej-Bawala NH-8A Village Matoda Tal-Sanand  Ahmedabad 382213
Industry Type : Pharma
Functional Area : R&D
End Date : 30th April, 2019

Require Quality Assurance Executive at Piramal Enterprises

Post : Executive Quality Assurance

Job Description
Knowledge of IPQA, Line Clearance for Manufacturing, Packing & Dispensing activity.  Sampling of Bulk and Finished goods, Review of production records and Finished Goods verification , on job training to the new people working in the production area, Statistical Process Monitoring, Online observation of process deviation and effective implementation of CAPA, Reporting of daily non conformance ,Daily verification of weighing balance calibration activity, Daily verification of environmental monitoring, verification and review of online Batch Manufacturing Records, Verification of production documents, Daily non conformance observation reported and maintained, knowledge of Change Control, Deviation, CAPA ,APQR, Stability study. Preparation of BMR/BPR. Validation and Qualification 

Special skill - Change control, Deviation ,CAPA,DCS, FSS Act 2006 regulation  

Any other information - Knowledge of Computer, SAP, Outlook.

Additional Information
Qualification : B.Pharm /M.Pharm
Location : Mahad  Piramal Enterprises Limited, Plot no. K-1 Additional M.I.D.C.  Mahad 402302
Industry Type : Pharma
Functional Area : Quality Assurance
End Date : 10th April, 2019

Require Senior Executive in Quality at Piramal Enterprises @ Apply now

Post : Senior Executive - Quality
Job Description
The Corporate Quality Assurance team is responsible for implementation of Corporate Quality Initiatives across all sites of Piramal Pharma Solutions, integration activities, corporate governance and audits, Data Integrity Compliance and Quench Management. As a critical member of the Corporate Quality Assurance team, your key responsibilities will include
• Responsible for integration of all newly acquired sites
• Handling projects under Corporate Quality Initiatives
* Annual Risk Assessment Compliance
* Quality Mindset
* Customer Centricity
* Audit Readiness
* Data Integrity Compliance
* Corporate Audits
• QMS maintenance and Quality Initiatives
* Audit Plan compliance
* Training compliance
* Management Overview
* Change control and deviations review
* SOP management
• Preparation and review of Corporate Guidelines/ Standard Operating Procedures/White Paper’s
• Support in preparation and hosting of Global Quality Meet
• Ensure rollout of Global software’s as assigned
• Support site and Corporate Quality team in various projects
• Responsible for Document Data Control and issuance & tracking.
• Ensure compliance to  QUENCH-Knowledge sharing portal
* Ensure that quality systems are in sync with current regulations by sharing updated regulatory guidance to all PEL sites
* Updating sites about warning letters and ensure compliance against each observation across PEL sites
• Any other tasks as assigned.
• Preparing and consolidating updates for Senior management

Candidate Profile
• B Pharm/M Pharm/MSc
•  Company with good regulatory track record
• Good communication skills/Fluent English
• Good exposure to GMP(Formulation and API).Sterile experience will be great.
• Should be able to have good experience on preparing Impactful PowerPoint presentations.
• Good collaboration,Commits and Delivers and Serves customer are skillsets
• Should have worked with Corporate team

Additional Information
Qualification : B.Pharm/M.Pharm/M.Sc
Location : Kurla  Project : Piramal Agastya, PRL Agastya Pvt Ltd., LBS Marg, Kamani Junction, Near Phoenix Mall, Kurla (West)  Mumbai 400070
Industry Type : Pharma
Functional Area : R&D
End Date : 28th February, 2019

Walk in Interview Piramal @ Banglore 1 September 2018