Friday 1 July 2016

Dr. Reddys Laboratories Ltd - Walk-in Drive for Method Validations On 03/07/16 @ Hyderabad


REFERENCE
Srinivasulu Tirumalasetty
Global pharma News

Dr. Reddy's Laboratories Ltd. - Walk-in Drive for Method Validations at Hyderabad for OSD and Injectables facilities at Visakhapatnam

Date: 3rd July, 2016 (Sunday)

Venue: 
Dr Reddys Laboratories Limited
Formulations Technical Operations 3 (FTO 3)
Survey No. 44, Bachupally,
Qutubullapur Mandal
Bachupally Campus,
Medak Dist 500 043

Contact person: KR Srinivas, Manager-HR

Qualification: M. Pharm, B. Pharm, M. Sc(min 60% is mandatory) 

Experience: 2 to 10 yrs

Following Safety procedures and practices at work place:

Strictly adherence to the practices and procedures (STPs, SOPs, SHE standards, JSAs & etc.,)
Maintenance of analytical equipments as per cGLP.
Performing instrument calibrations as per the schedule.
Conducting Dissolution profile analysis as per the analytical request.
Analysis of confirmatory batch, hold study and development related samples.
Training to new joiners during analysis.
Performing analysis by following online documentation practice.
Preparation of method validation protocols and reports.
Execution of method validation and transfer activity as per the protocol.
Review of analytical documents produced by team members.
Producing error free documents.
Escalation of issues in online to group leader. Highlighting the requirements to Group leader in right time.
Performing Method validations as per the protocol
Preparation of data compilation & relevant reports.
Maintenance of Instrument spares.

Area of Responsibilities: 
Work experience in Analysis of Pharmaceutical samples.
Having knowledge on analytical methods, instrumentation and calibrations.
Well versed with analytical instrumentation like HPLC, GC, Dissolution, UV, IR spectrophotometers etc.

Should have hands on experience on various analytical equipments calibrations.
Should have experience and capable of online documentation and following lab compliance.
Should have good knowledge of cGMP and cGLP.

Note:  Minimum of two years of experience in current or previous company is mandatory

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