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PHARMA WISDOM

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Tuesday 31 July 2018

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VIMTA LABS - Urgent Walk-Ins for B.Sc / B.Com / BA Freshers & Experienced Candidates on 1st August, 2018 @ Hyderabad

20:29:00 1
Required B.Com / B.Sc. / BA graduates Fresher's or Experienced with very good communication skills for Project Management role.
Job is based at Hyderabad location.
Interested candidates can send their cvs to suryavamsi.vasireddy@vimta.com
Salary / CTC is negotiable.
If you are localite of Hyderabad and you can come down for face to face round of interview on 1st of Aug at 1 PM.
Venue:
VIMTA Life Sciences
Genome valley
MN Park
Turkapally,
Medchal
Malkajgiri mandal
Hyderabad .
Documents to carry for interview:
- Updated CV
- Educational certificates photocopies
- Two passport size photographs
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Urgent Openings in AR&D / Stores / Warehouse / Purchase Departments @ Biophore India Pharmaceuticals Pvt. Ltd

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Divis Laboratories Limited - Campus Interviews on 1st August, 2018 @ KHAMMAM COLLEGE OF PHARMACY, KHAMMAM

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Granules India Limited - Walk-In Interview for Assistant Manager - QC on 1st August, 2018 @ Hyderabad

14:33:00 0
Walk-In Interview for Asst. Manager – QC @ Granules India Ltd, Hyderabad
Date & Time: 1st August, 9 AM onwards
Venue:
Granules India Limited,
Plot No 15A/1, Phase - III,
IDA, Jeedimetla,
Near Bus Depot,
Hyderabad -500055
Department: Quality Control
Position: Asst. Manager
Experience: 7 – 10 years
Job Location: Hyderabad
Job Description:
- Monitoring of cGLP followed by laboratory personnel during routine operations to ensure adherence to procedure.
- Ensuring training of analysts in Laboratory techniques, Quality Control procedures and principles of cGLP / cGMP /General analytical methods instrumentation etc.
- Implementation QMS
- Qualification of Laboratory Instruments (IQ/OQ/PQ)
- Planning of day to day Laboratory activities
- Maintain Real time documentation and Laboratory safety around the clock
- Review of analytical documents followed as per cGMP and Quality Policies.
- Preparation and Responsible to peer-review of Stability Protocols, compile the stability data.
- Coordinating with Regulatory Affairs and fulfilling their requirements with respect to filling of new drug products and annual updating.
- Handling of customer complaints
- Checking the audit trails and analytical reports.
- Responsible for GLP compliance in the QC Department
- Preparation and review of Method transfer/Validation protocols
- Review of Instrument Calibration data
- Handling of Incidents, OOS, Change controls, OOT and all other cGMP record.
- Implementation of CAPAs
- Monitoring implementation of changes as per change control.
- Stability Management
- Preparation and review of specification and test procedures (STPs), General test procedures (GTPs) and cleaning methods.
- Preparation and review of Standard operating procedures (SOPs) and Validation Protocols.
- Review of Analytical Raw data sheets With respect to STPs, GTPs and SOPs.
- Preparation of Certificate of Analysis (COA) for Finished Products, and for Raw materials and intermediates.
- Review of BPCRs
- Preparation and review of Lab Metrics.
- Conducting the analyst qualifications periodically for the all the analysts in QC as per the schedule.
- Timely support to the regulatory activities in view of Revision of specifications and Test Methods
- Conducting the functional trainings and on job trainings to the employees in QC as per the schedule with evaluation.
- Responsible for compliance of Customer and regulatory Audits

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