SOLARA (Strides Chemicals) - Walk-In Interviews for Quality Control on 22nd Mar' 2019 - PHARMA WISDOM

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Tuesday, 19 March 2019

SOLARA (Strides Chemicals) - Walk-In Interviews for Quality Control on 22nd Mar' 2019


Walk-In for Quality Control (API) Ambernath for Usfda Approved Plant
Company: Solara Active Pharma Sciences Limited
Date & Time: 22nd March , 9 AM onwards
Venue
Strides Chemicals Private Limited (A Subsidiary of Solara) Formerly known as Perrigo API India Pvt. Ltd.
Plot No - 39, Anand Nagar MIDC, Additional Ambernath,
Ambernath East, Pin 421506, Mumbai, India
Walk-In for Quality Control (API) Ambernath for USFDA Approved Plant for below positions -
1. Position - Executive - Quality Control (Shift Analyst)Education / Experience - M.Sc / 3 to 6 year
Job Description -
- Performing analysis with use of sophisticated analytical instruments like HPLC, GC, UV, IR, Polarimeter, Particle size analyzer, Autotitrator, KF titrator etc. for water analysis, raw material, packaging material, intermediates, in process, finished product as per standard testing procedure.
- Calibration and maintenance of instruments.
- Preparations of working standard, retention samples and maintain their records as per SOP.
- Good knowledge of cGMP, GLP, GDP and QMS.
- Knowledge of Instrument Software's like LIMS, Empower, etc. desired.
- Good Communication & Interpersonal Skill.
2. Position - Team Leader Quality Control (Instrumentations & Calibrations)
Education / Experience - M.Sc / 8 to 10 years 

Job Description -
- Performing routing Testing, Calibration and Qualification activities.
- Protocol writing and review of validation, calibration and qualification documents.
- Handle Instrumentation for LC, GC, KF, PSD, UV,IT, Potentiometer, etc.
- Calibration and maintenance of instruments.
- Knowledge of Wet Chemistry & CSV activities desired.
- Good knowledge of cGMP, GLP, GDP and QMS.
- Good Communication & Interpersonal Skills.
3. Position - Team Leader Quality Control (Reviewer)
Education / Experience - MSc / 8 to 10 years

Job Description -
- Review of all analytical data, log books, sequences of HPLC and GC.
- Review the specifications, method of analysis and analytical protocols.
- Review OOS, OOT, Deviations and QC Documentation.
- Review of QC registers, finished product, in-process, Protocol tracking, working standard, column usage and primary standard usage.
- Good knowledge of cGMP, GLP, GDP and QMS.
- Good Communication & Interpersonal Skills.

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